NXTS 10-K & 10-Q changes, risk factors and insider trading
Nexentis Technologies Inc. · Nasdaq · Pharmaceutical Preparations · CIK 1789192 · All filings on SEC.gov
At a glance
What changed in the latest 10-K
Risk Factors
New heading “Risks Related to Business Operations of MitoCareX”
New heading “MitoCareX has no operating history.”
New heading “MitoCareX will require substantial additional capital to finance its operations, and a failure to obtain this necessary capital when needed on acceptable terms, or at all, could force it to delay, limit, reduce, or terminate ACSMT development programs, MITOLINE™ related validations and optimizations, commercialization efforts or other operations.”
New heading “Raising additional capital may restrict MitoCareX’s operations, or require it to relinquish rights to its ACSMT or other technologies.”
New heading “MitoCareX is early in its development efforts. All of its ACSMT programs are still in the preclinical or discovery stage. Its MITOLINE™ algorithm requires further validations and optimizations. If MitoCareX is unable to successfully develop, obtain regulatory approval, and ultimately commercialize any current or future ACSMT or its MITOLINE™ algorithm, or experience significant delays in doing so, its business will be materially harmed.”
New heading “Conditions in Israel and regional instability may adversely affect our operations.”
New heading “If we fail to comply with the continued listing requirements of the Nasdaq Capital Market, our common stock may be delisted and the price of our common stock and our ability to access the capital markets could be negatively impacted.”
Removed heading “Because of our limited operating history, we may not be able to successfully operate our business or execute our business plan.”
Removed heading “Our customers require that our products undergo a lengthy testing period without any assurance of sales.”
Removed heading “Our products and technology require additional trials.”
Removed heading “The commercial success of our new generation products, as well as any future products, depend upon the degree of market acceptance by the packing house community as well as by other prospect markets and industries.”
Removed heading “We may face significant competition from other companies looking to develop or acquire new alternative environmentally friendly solutions for the treatment of fruits and vegetables, and other edible matter.”
Removed heading “Our success is dependent upon the acceptance of our environmentally friendly solutions for fruits and vegetables.”
Removed heading “We may be unable to respond effectively to technological changes in our industry, which could reduce the demand for our products.”
Removed heading “We currently rely on a limited number of suppliers to produce certain key components of our products.”
Removed heading “If we are unable to establish sales, marketing and distribution capabilities or enter into successful relationships with third parties to perform these services, we may not be successful in commercializing our products.”
Removed heading “We rely on rapidly establishing a global distributorship network in order to effectively market our products.”
Removed heading “The results of our early tests may not be indicative of results in future tests and we cannot assure you that any planned or future tests will lead to results sufficient for the necessary regulatory approvals.”
Removed heading “Our products are highly regulated by governmental agencies in the countries where we conduct business and in countries in which we plan to expand. Our failure to obtain regulatory approvals and registration, to comply with registration and regulatory requirements or to maintain regulatory approvals would have an adverse impact on our ability to market and sell our products.”
Removed heading “Our success is dependent upon our ability to achieve regulatory approvals and registration in the United States, Mexico, Peru, Brazil, and Israel, which might take longer than expected.”
Removed heading “The inherent dangers in production and transportation of hydrogen peroxide and highly concentrated organic acids could cause disruptions and could expose us to potentially significant losses, costs or other liabilities.”
Removed heading “Our business and operations may be affected by unexpected events, including climate change conditions and natural disasters, which could materially harm our financial results.”
Removed heading “We are subject to risks relating to portfolio concentration.”
Removed heading “Our operating results may fluctuate, which makes our results difficult to predict and could cause our results to fall short of expectations.”
Removed heading “International expansion of our business exposes us to business, regulatory, political, operational, financial and economic risks associated with doing business outside of the United States, Mexico or Israel.”
Removed heading “Our business depends to some extent on international transactions.”
Removed heading “Risks Related to NTWO OFF”
Removed heading “The evolution of our business strategy may not be successful and we may require additional financing, have increased operational costs or other financial harm to our business and financial condition.”
Removed heading “If NTWO OFF becomes subject to environmental-related claims, it could incur significant cost and time to comply.”
Removed heading “NTWO OFF requires certain permits to operate its nitrous oxide business. If NTWO OFF is unable to obtain or renew such permits it will adversely impact our operations.”
Removed heading “NTWO OFF is an early-stage company and we can provide no assurance of the successful and timely development of its products.”
Removed heading “Conditions in Israel, including Israel’s conflicts with Hamas and other parties in the region, as well as political and economic instability, may adversely affect our operations and limit our ability to market our products, which would lead to a decrease in revenues.”
Removed heading “If we fail to comply with the Nasdaq Capital Market listing requirements, we will be subject to potential delisting from the Nasdaq Capital Market.”
Largest changes
The recent historically high inflation in the U.S., geopolitical issues, continuous increases in interest rates, unstable global conditions and changes in exchange rates have led to global economic instability.see in full comparisonAlthoughMacroeconomicdemandconditionsformayfreshadverselyhorticultural products is considered inelastic in developed economies,affect thefreshindustriesproducein which we operate, including the biotechnology andcitrusrenewableindustriesenergythatsectors.weInflation,sellrisingto may be affected by material changes in supply, market prices, exchangeinterest rates andgeneralvolatility in global financial markets may increase our research and development expenses, raise the cost of materials and services, disrupt supply chains or limit our access to capital. In addition, higher interest rates and economicconditions.uncertaintyAsmayareduceresultinvestments in renewable energy projects and slow the pace ofthe high inflationdevelopment andrecession, we are seeing record high levelscommercialization ofunemploymentnew technologies. andconsumer spending trends are changing. Delays or reductions in our customers’ purchasing or shifts to lower-cost alternatives that result from tighter economic market conditions would reduce demand for our products and services andcould, consequently, have a material adverse effect on our business, financial condition and results of operations. Moreover, the new Trump administration has recently imposed tariffs on certain U.S. imports, and indicated that he would impose a 25% tariff against all goods imported from Canada and Mexico, and a 10% tariff on certain imports from China; China and other countries have responded with retaliatory tariffs on certain U.S. exports. We cannot predict what effects these tariffs and potential additional tariffs will have on our business. However, these tariffs and other trade restrictions could increase our operating costs, reduce our gross margins or otherwise negatively impact our financial results. Changes in international trade policies, tariffs or other restrictions on imports of equipment or materials used in our technologies could also increase our operating costs or otherwise negatively affect our financial results. Any of the foregoing factors could have a material adverse effect on our business, financial condition and results of operations.
“If we fail to comply with the continued listing requirements of the Nasdaq Capital Market, our common stock may be delisted and the price of our common stock and our ability to access the capital markets could be negatively impacted.”see in full comparison
“If we fail to comply with the Nasdaq Capital Market listing requirements, we will be subject to potential delisting from the Nasdaq Capital Market.”see in full comparison
“Regional instability and armed conflict may have broader adverse effects on economic and financial conditions in Israel, including effects on credit markets, currency valuation, inflation, and labor markets. Prolonged conflicts have in the past required significant mobilization of military reservists, including personnel employed in the sector in which we operate, which may affect workforce availability across the industry. Such conditions may also result in credit rating changes for Israel, which could adversely affect access to capital and general business conditions.”see in full comparison
“We have in the past fallen out of compliance with certain continued listing standards including the minimum bid price requirement although we have subsequently been able to regain compliance. No assurance however can be given that we will continue to be in compliance with the continued listing requirements of the Nasdaq Capital Market. Failure to meet applicable Nasdaq continued listing standards could result in a delisting of our common stock. …”see in full comparison
“In addition, new laws and regulations may be introduced, or existing laws and regulations may be changed or may become subject to new interpretations, which could result in additional compliance costs, seizures, confiscations, recalls, monetary fines or delays that could affect us or our customers.”see in full comparison
Full comparison: every changed paragraph (130)
If
we are unable to successfully complete the MitoCareX acquisition, or future acquisitions or to effectively integrate NTWO OFF or future
acquisitions, our ability to grow our business or to operate our business effectively could
be reduced, and our business, financial condition
and operating results could suffer. Even if we are successful in completing acquisitions,
we cannot assure that we will be able to integrate
the operations of the acquired business without encountering difficulty regarding
different business strategies with respect to marketing
and integration of personnel with disparate business backgrounds and corporate
cultures. The integration of NTWO OFF,MitoCareX, which was incorporated
in AugustFebruary 2023,2022, is still in progress and, we cannot assure that such
process will be completed without encountering difficulties. Further,
in certain cases, mergers and acquisitions require special approvals,
or are subject to scrutiny by the local authorities, and failing
to comply with such requirements or to receive such approvals, may prevent
or limit our ability to complete the acquisitions as well
as expose us to legal proceedings prior or following the consummation of such
acquisitions. In some cases, such proceedings, if initiated,
may conclude in a requirement to divest portions of the acquired business.
Because
of our limited operating history, we may not be able to successfully operate our business or execute our business plan.
In
September 2018, we changed our organizational structure and management team. After reviewing our company then existing strategy and results
of operation, as well as examining market opportunities, the new management team decided to update our strategy, reduce the marketing
and sales of its existing products, and focus our efforts and financial resources on developing its next generation of products. From
2019 to 2020, we developed, validated and tested the efficacy of our next generation product - a blend of food acids - on a variety of
crops in both small- and large-scale commercial pilots. In the years 2021 through 2022, we commenced commercialization in various jurisdictions,
while continuing to conduct commercial pilots. In 2023, the Company decided to reduce Save Foods Ltd.’s research and development
activities and focus on existing markets. In 2024, the Company expanded its pilots in Peru and Brazil and made initial efforts to enter
the Ethiopian market.
Given
our limited operating history, it is hard to evaluate our proposed business and prospects. Our proposed business operations will be subject
to numerous risks, uncertainties, expenses and difficulties associated with early-stage enterprises. Such risks include, but are not
limited to, the following:
Because
we are subject to these risks, evaluating our business may be difficult, our business strategy may be unsuccessful and we may be unable
to address such risks in a cost-effective manner, if at all. If we are unable to successfully address these risks our business could
be harmed.
Our
customers require that our products undergo a lengthy testing period without any assurance of sales.
Our
prospective customers generally test and evaluate our solutions before applying them to their commercial product lines or integrating
them into their facilities. This testing period takes at least two seasons and could be longer or subject to delays. Even after our solutions
are approved by the customers, due to seasonal effects, it could take several months before they begin purchasing our solutions, if at
all. Nothing guarantees that following such pilots, the targeted packing house will choose to use our solutions on its products or continue
the process further and complete the sale cycle. The combination of the longer sales cycle and the unique nature of our solutions that
could have different results following seasonal changes could have an impact on our profitability and business. As a result, we could
have limited revenues, or no revenues, from prospective customers, even after we have invested significant amounts of time in the pilot
phase and sales of our solutions, which in turn could adversely affect our business and financial results.
Our
products and technology require additional trials.
The
efficacy of our products has only been shown in the limited number of pathogens tested on certain produce and climates, and therefore
our products have yet to be proven against certain additional pathogens, produce and market climates to validate the efficacy and benefits
of our products. These trials are lengthy and prolong our sale cycle by at least two seasons, and no assurance can be made that such
packing facilities will chose to implement our solutions in their facilities.
The
commercial success of our new generation products, as well as any future products, depend upon the degree of market acceptance by the
packing house community as well as by other prospect markets and industries.
To
achieve high volume sales and attain a leading market share and become the new standard of treatment, our products must not only be approved
by the regulators, but also endorsed by the major packing houses and service providers, retailers of fruits and vegetables as well as
environmental organizations. Our success depends on our ability to create significant value to the growers, the packing houses and the
food retailers. We are aware of this key factor and are focusing on conducting large scale pilots with major fruits and vegetables packers
and retail suppliers of fresh consumed goods in several countries to show the efficacy of the products and our technology, and to receive
the recognition of packers and retailers. However, there can be no assurances that we will succeed in such an endeavor, nor is it clear
how long it will take until we receive market recognition.
There
can be no assurance that any product that we bring to the market will gain market acceptance by prospective customers. The commercial
success of our new generation products and any future product depends in part on the packing house community as well as other industries
for various use cases, depending on the acceptance by such industries of our technology as a useful and cost-effective solution compared
to current solutions. If our new generation products or any future product do not achieve an adequate level of acceptance, we may not
generate significant product revenue and may not become profitable. The degree of market acceptance of our products will depend on a
number of factors, including:
Our
efforts to penetrate the packing house industry and educate the marketplace on the benefits of our products may require significant resources
and may never be successful.
We
may face significant competition from other companies looking to develop or acquire new alternative environmentally friendly solutions
for the treatment of fruits and vegetables, and other edible matter.
We
expect to face significant competition in every aspect of our business, and particularly from other companies that seek to enter our
focal market. As regulators continue to move away from current residue chemical solutions, such as chlorpropham or CIPC, existing suppliers
of these solutions are continually looking to develop or acquire new alternative environment-friendly solutions that can sustain their
market share and revenue streams, or to enable the continuance of CIPC at current levels in new ways of treatment. Additionally, as market
opportunity becomes eminent, competitors and new players will most likely attempt to develop similar or comparable solutions. It is possible
that superior or more cost-effective alternative technology will emerge that will achieve greater market acceptance and render our products
less competitive. Furthermore, existing vendors can cooperate to combat new players by reducing market prices and margins or other competitive
initiatives. Our future success will therefore depend, to a large extent, upon our ability to achieve market acceptance of our innovative
solutions as well as develop and introduce new products and enhancements to existing products. No assurance can be given that we will
be able to compete in such a marketplace.
The
market for post-harvest solutions is fragmented with various regional suppliers. The market of post-harvest treatments for fruits and
vegetables is dominated by five large players with wide reach across the globe, which players may perceive us as a competitive threat
and institute commercial measures to reduce our market share, including by aggressively ‘bundling’ their products and services
to compete with us. We believe that the principal competitive factors in our industry include reputation, product quality, customer service
and customer intimacy, product innovation, technical service, and value creation.
Our
success is dependent upon the acceptance of our environmentally friendly solutions for fruits and vegetables.
Our
future success is dependent upon the acceptance of our environmentally friendly, non-toxic residual solutions for fruits and vegetables.
While the market is signaling that such a direction is likely, certain trends as well as the future size of this market, and other potential
markets for our products, rely upon a number of factors, many of which are beyond our control. For example, both the failure to convince
retailers to bear additional costs for “green” fruit and vegetables as well as the failure to persuade consumers to purchase
“green” fruits and vegetables for higher prices may adversely affect our business, financial condition, operating results
and cash flow going forward.
We
may be unable to respond effectively to technological changes in our industry, which could reduce the demand for our products.
Our
future business success will depend upon our ability to maintain and enhance our technological capabilities and develop and market products,
services and applications that meet changing customer needs and market conditions in a cost-effective and timely manner. Maintaining
and enhancing technological capabilities and developing new products may also require significant investments in research and development,
which following financial cutbacks, we have shifted our focus to the commercialization of our solutions with emphasis on converting recently
completed pilots into paying customers. We may not be successful in converting our completed pilots into paying customers or to develop
new products, services and technology that successfully compete or are able to anticipate changing customer needs and preferences, and
our customers may not accept one or more of our new products or services. If we fail to keep pace with evolving technological innovations
or fail to modify our products and services in response to customers’ needs or preferences, then our business, financial condition
and results of operations could be adversely affected.
We
currently rely on a limited number of suppliers to produce certain key components of our products.
We
rely on unaffiliated contract manufacturers to produce certain key components of our products. In Israel, we work exclusively with a
well-known producer of chemicals, Zohar Dalia, who is responsible for the production of our products. Zohar Dalia is well known for its
knowledge and handling of hydrogen peroxide. In the United States, we have worked for the past few years with Seeler Industries, a national
leader in the marketing and handling of hydrogen peroxide. There is limited available manufacturing capacity that meets our quality standards
and regulatory requirements, especially for the manufacturing of the SF3H and SF3HS with one of their active ingredients - hydrogen peroxide
- as well as for FreshPROTECT with one of its active ingredients - PO3. If we are unable to arrange for sufficient production capacity
among our contract manufacturers or if our contract manufacturers encounter production, quality, financial, or other difficulties, including
labor or geopolitical disturbances, we may encounter difficulty in meeting customer demands as we seek alternative sources of supply,
or we may have to make financial accommodations to such contract manufacturers or otherwise take steps to mitigate supply disruption.
We may be unable to locate an additional or alternate contract manufacturer that meets our quality controls and standards and regulatory
requirements in a timely manner or on commercially reasonable terms. Any such difficulties could have an adverse effect on our business,
financial condition and results of operations, which could be material.
If
we are unable to establish sales, marketing and distribution capabilities or enter into successful relationships with third parties to
perform these services, we may not be successful in commercializing our products.
We
have a limited selling and marketing infrastructure and have limited experience in the sale, marketing or distribution of products. To
achieve commercial success for any product for which we have obtained marketing approval, we will need to enter into collaborations with
third parties, like post-harvest service companies, and establish a selling and marketing infrastructure or to out-license our products.
In
the future, we may consider building a focused selling and marketing infrastructure to market our products in the United States or elsewhere
in the world. There are risks involved with establishing our own sales, marketing and distribution capabilities. For example, recruiting
and training a sales force could be expensive and time consuming and could delay any product launch. This may be costly, and our investment
may be lost if we cannot retain or reposition our selling and marketing personnel.
Factors
that may inhibit our efforts to commercialize our products on our own include:
If
we are unable to establish our own sales, marketing and distribution capabilities or enter into successful arrangements with third parties
to perform these services, our revenues and our profitability may be materially adversely affected.
In
addition, we may not be successful in entering into arrangements with third parties to sell, market and distribute our products in our
target markets, including Chile, Mexico, Peru, the United States, Brazil and Israel, or may be unable to do so on terms that are favorable
to us. We likely will have little control over such third parties, and any or all of them may fail to devote the necessary resources
and attention to sell and market our products effectively. If we do not establish sales, marketing and distribution capabilities successfully,
either on our own or in collaboration with third parties, we may not be successful in commercializing our product candidates.
We
rely on rapidly establishing a global distributorship network in order to effectively market our products.
We
have developed initial partnerships with local partners. In order to expand selling and marketing globally and capture leading market
share before any potential reaction from competitors, we will need to rapidly expand geographically and establish a global distribution
network. This will likely put pressure on our management as well as on our financial and operational resources. To mitigate this factor,
once we establish a significant presence in the market, we will proceed to establish strategic partnerships with leading market players;
however, there are no assurances that we will succeed in establishing such partnerships, which may harm the marketing of our products
and the development of our business.
The
results of our early tests may not be indicative of results in future tests and we cannot assure you that any planned or future tests
will lead to results sufficient for the necessary regulatory approvals.
Our
products have been tested in multiple commercial and small-scale pilots on certain types of produce and during specific times of the
year. We are currently in the development and optimization phases of these products. Results from our later-stage commercial tests may
show lower efficacy than our early-tests conducted previously, and we cannot guarantee that when commercialized, our products will be
effective and stable and product improvements as well as possible changes in the application and usage protocol may be required. Our
results could further be affected by the changing behavior of the fruits throughout the season, therefore demonstrating inconsistent
results. These factors may significantly delay receipts of regulatory approvals, and the introduction of our products into the market.
Likewise, we cannot be sure these products will be commercially viable and have no assurances that we will be able to expand upon our
current product offerings or that any such expansion will generate revenue.
Our
products are highly regulated by governmental agencies in the countries where we conduct business and in countries in which we plan to
expand. Our failure to obtain regulatory approvals and registration, to comply with registration and regulatory requirements or to maintain
regulatory approvals would have an adverse impact on our ability to market and sell our products.
Some
of our products are subject to technical review and approval by government authorities in each country where we currently conduct our
business and where we intend to sell our products.
The
regulatory requirements to which we are subject are complex and vary from country to country. To obtain new registrations, it is necessary
to have a local registrant, and to understand the country’s regulatory requirements, both at the time an application for registration
is submitted and when the registration decision is made, which may be several years later. A significant investment in registration data
is required (covering all aspects from manufacturing specifications through storage and transport, use, and disposal of unwanted product
and used containers) to ensure that product performance (e.g., efficacy), intrinsic hazards and use patterns are fully characterized.
Risk assessments are conducted by government regulatory authorities who make the final decision on whether the documented risk associated
with a product and active ingredient is acceptable prior to granting approval for sale. This process may be prolonged due to requirements
for additional data or internal administrative processes. There is a risk that registration of a new product may not be obtained or that
a product label may be severely reduced, restricting the use of the product. If these circumstances arise, there is a risk that the substantial
investments made in product development will generate the projected sales that justified the investment, and our business, financial
condition and results of operations may be adversely affected by failure to obtain new registrations.
Products
that are already approved may be subject to periodic review by regulatory authorities in many countries. Such reviews frequently require
the provision of new data and more complex risk assessments. The outcome of such reviews of existing registrations cannot be guaranteed
and registrations may be modified or canceled. Since all government regulatory authorities have the right to review existing registrations
at any time, the sustainability of the existing portfolio cannot be guaranteed. Existing registrations may be lost at any time, resulting
in an immediate impact on sales. Furthermore, prior to expiration, it is necessary to renew registrations. The renewal period and processes
vary by country and may require additional studies to support the renewal process. Failure to comply could result in cancellation of
the registration, resulting in an impact on sales.
In
addition, new laws and regulations may be introduced, or existing laws and regulations may be changed or may become subject to new interpretations,
which could result in additional compliance costs, seizures, confiscations, recalls, monetary fines or delays that could affect us or
our customers.
Our
success is dependent upon our ability to achieve regulatory approvals and registration in the United States, Mexico, Peru, Brazil, and
Israel, which might take longer than expected.
We
are subject to extensive national, state and local government regulation. A critical key to our success and ability to expand our business
is our ability to obtain regulatory approvals and registration in the United States and in other countries for the use of our products.
The regulatory approvals of some of our products are dependent on trials to show the efficacy and the non-toxicity of our products and
are time and cost consuming. We do not anticipate any significant problems in obtaining future required licenses, permits or approvals
that are necessary to expand our business, however such licenses, permits or approvals may take longer than expected due to various factors,
which might cause delays in these countries and other jurisdictions.
We
do not have backlogs or firm commitments from our customers for our products. Our sales may deteriorate if we fail to achieve commercial
success or obtain regulatory approval of any of our products.
The
inherent dangers in production and transportation of hydrogen peroxide and highly concentrated organic acids could cause disruptions
and could expose us to potentially significant losses, costs or other liabilities.
Our
operations are subject to significant hazards and risks inherent to the transportation of the active ingredient of one of our products
- hydrogen peroxide. In high concentrations, our blend of acids has a very low pH which may lead to skin burn and hydrogen peroxide is
an aggressive oxidizer and both can corrode many materials. We are working with limited low concentration of the material, however in
high concentrations of H2O2 it will react violently. Hydrogen peroxide should be stored in a cool, dry, well-ventilated
area and away from any flammable or combustible substances. It should be transported in special tanks and vehicles and should be stored
in a container composed of non-reactive materials. These hazards and risks include, but are not limited to fires, explosions, third-party
interference (including terrorism) and mechanical failure of equipment at our or third-party facilities. The occurrence of any of these
events could result in production and distribution difficulties and disruptions, personal injury or wrongful death claims and other damage
to properties.
Our
business and operations may be affected by unexpected events, including climate change conditions and natural disasters, which could
materially harm our financial results.
Unexpected
events, including fires or explosions at our facilities, natural disasters such as earthquakes and wildfires, unplanned power outages,
supply disruptions, failure of equipment or systems, and severe weather events, such as droughts, heat waves, hurricanes, and flooding,
could adversely affect our reputation and results of operations through physical damage to our facilities and equipment and through physical
damage to, or disruption of, local infrastructure or disrupt our operations generally. During the past several years we have seen an
increase in the frequency and intensity of severe weather events and we expect this trend to continue due to climate change.
Our
business, in particular, may be affected from changes in climate conditions as such events would affect the crops yield and their storability
in those cases where there is unusually warm, dry, humid or cold weather before cropping.
In
such instances, we may suffer a decrease in revenues as a result of a smaller storage volume of rooms or shorter storage period. We anticipate
that once we increase our operations and enter certain markets which experience or will experience significant climate change, such as
above-common rain fall, heat waves, dry air conditions, and unusually cold or prolonged cold weather conditions, such events may materially
impact our financial results.
Furthermore,
certain natural disasters may affect our operations. Given that our operations are global in nature, and our partnerships are located
in various geographic locations subject to certain inherent dangers, it is plausible that our business and operations may be adversely
affected by any such future natural disasters.
The
recent historically high inflation in the U.S., geopolitical issues, continuous increases in interest rates, unstable global conditions
and changes in exchange rates have led to global economic instability. AlthoughMacroeconomic demandconditions formay freshadversely horticultural products is considered
inelastic in developed economies,affect the freshindustries producein
which we operate, including the biotechnology and citrusrenewable industriesenergy thatsectors. weInflation, sellrising to may be affected by material changes in supply,
market prices, exchangeinterest rates and generalvolatility in global
financial markets may increase our research and development expenses, raise the cost of materials and services, disrupt supply chains
or limit our access to capital. In addition, higher interest rates and economic conditions.uncertainty Asmay areduce resultinvestments in renewable energy
projects and slow the pace of the high inflationdevelopment and recession, we are seeing record
high levelscommercialization of unemploymentnew technologies. and consumer spending trends are changing. Delays or reductions in our customers’ purchasing or shifts
to lower-cost alternatives that result from tighter economic market conditions would reduce demand for our products and services and
could, consequently, have a material adverse
effect on our business, financial condition and results of operations. Moreover, the new
Trump administration has recently imposed tariffs
on certain U.S. imports, and indicated that he would impose a 25% tariff against all
goods imported from Canada and Mexico, and a 10%
tariff on certain imports from China; China and other countries have responded with
retaliatory tariffs on certain U.S. exports. We cannot
predict what effects these tariffs and potential additional tariffs will have
on our business. However, these tariffs and other trade
restrictions could increase our operating costs, reduce our gross margins or
otherwise negatively impact our financial results. Changes
in international trade policies, tariffs or other restrictions on imports of equipment or materials used in our technologies could also
increase our operating costs or otherwise negatively affect our financial results. Any of the foregoing factors could have a material
adverse effect on our business, financial condition and results of operations.
Risks Related to Business Operations of MitoCareX
MitoCareX has no operating history.
MitoCareX is a drug discovery and development company with a current focus on oncology with a limited operating history upon which you can evaluate its business and prospects. MitoCareX commenced operations in 2022, has no products approved for commercial sale, and has not generated any revenue from the sale of its products. To date, MitoCareX has focused primarily on organizing and staffing its company, business planning, raising capital, building its proprietary computational platform, discovering potential Anti-Cancer Small Molecule Therapeutics (ACSMT), establishing its intellectual property portfolio, conducting research, establishing arrangements with third parties for the manufacture of ACSMT and supply of related raw materials, and providing general and administrative support for these operations. Its scientific approach to the discovery and development of ACSMT is unproven and MitoCareX does not know whether MitoCareX will be able to develop or obtain regulatory approval for any products of commercial value. MitoCareX has only one type of chemical scaffold of ACSMT in early development. MitoCareX has not yet completed any preclinical and clinical trials, successfully developed and validated a diagnostic test, obtained regulatory approvals, manufactured products on a commercial scale, or arranged for a third party to do so on its behalf, or conducted sales or marketing activities necessary for successful product commercialization. Consequently, any predictions made about its future success or viability may not be as accurate as they could be if MitoCareX had a history of successfully developing and commercializing biopharmaceutical products.
MitoCareX has incurred significant operating losses since its inception and expects to incur significant losses for the foreseeable future. MitoCareX does not have any products approved for sale and has not generated any revenue since its inception. If MitoCareX is unable to successfully develop and obtain the requisite approval for and commercialize ACSMT, MitoCareX may never generate revenue. MitoCareX incurred net losses of $1,394,000 and $886,000 for the year ended December 31, 2025 and for the year ended December 31, 2024, respectively. As of December 31, 2025, MitoCareX had an accumulated deficit of $3,154,000. Substantially all of its losses have resulted from expenses incurred in connection with its research and development programs and from general and administrative costs associated with its operations. ACSMT will require substantial additional development time and resources before MitoCareX would be able to apply for or receive regulatory approvals and begin generating revenue from product sales. MitoCareX expects to continue to incur losses for the foreseeable future, and MitoCareX anticipates these losses will increase substantially as MitoCareX continues its development of, seeks regulatory approval for, and potentially commercializes ACSMT and seeks to discover and develop additional solutions as well as operate as a public company.
To become and remain profitable, MitoCareX must succeed in discovering, developing, obtaining regulatory approvals for, and eventually commercializing products that generate significant revenue. This will require MitoCareX to be successful in a range of challenging activities, including preclinical studies and completing clinical trials of ACSMT, discovering additional ACSMTs, obtaining regulatory approval for these and manufacturing, marketing, and selling any products for which MitoCareX may need to obtain regulatory approval. MitoCareX is in the preliminary stages of these activities. MitoCareX may never succeed in these activities and, even if MitoCareX does, it may never generate revenue that is significant enough to achieve profitability. In addition, MitoCareX has not yet demonstrated an ability to successfully overcome many of the risks and uncertainties frequently encountered by companies in new and rapidly evolving fields, particularly in the biopharmaceutical industry. Because of the numerous risks and uncertainties associated with biopharmaceutical product development, MitoCareX is unable to accurately predict the timing or amount of increased expenses or when, or if, MitoCareX will be able to achieve profitability. Even if MitoCareX does achieve profitability, MitoCareX may not be able to sustain or increase profitability on a quarterly or annual basis. Its failure to become and remain profitable may have an adverse effect on its value and could impair its ability to raise capital, expand its business, maintain its research and development efforts, diversify its ACSMT pipeline, achieve its strategic objectives, or even continue its operations. A decline in the value of MitoCareX could also cause you to lose all or part of your investment.
MitoCareX will require substantial additional capital to finance its operations, and a failure to obtain this necessary capital when needed on acceptable terms, or at all, could force it to delay, limit, reduce, or terminate ACSMT development programs, MITOLINE™ related validations and optimizations, commercialization efforts or other operations.
The development of ACSMT, including conducting preclinical studies and clinical trials, is a very time-consuming, capital-intensive, and uncertain process. Since its acquisition in October 2025, MitoCareX’s operations have continued to consume substantial amounts of cash. The Company expects that MitoCareX’s expenses to substantially increase in connection with MitoCareX ongoing activities, particularly when MitoCareX will conduct its ongoing and planned preclinical studies and clinical trials and potentially seeks regulatory approval for its ACSMT and any future ACSMT MitoCareX may develop. If MitoCareX obtains regulatory approval for ACSMT, the Company expects that MitoCareX’s to incur significant commercialization expenses related to product manufacturing, marketing, sales, and distribution. Because the outcome of any preclinical study or clinical trial is highly uncertain, MitoCareX cannot reasonably estimate the actual amount of capital necessary to successfully complete the development and commercialization of ACSMT.
The Company will need to obtain substantial additional funding to support MitoCareX’s continuing operations. The ability to raise additional funds may be adversely impacted by global economic conditions, disruptions to, and volatility in, the credit and financial markets in the United States, inflation, diminished liquidity and credit availability, declines in consumer confidence, declines in economic growth, increases in unemployment rates, and uncertainty about economic stability. If the equity and credit markets deteriorate, it may make any necessary debt or equity financing by the Company more difficult, more costly, and more dilutive. If additional capital cannot be raised when needed or on attractive terms, the Company could be forced to delay, reduce, or eliminate MitoCareX’s research and development programs or any future commercialization efforts, or even cease operations.
The Company may also seek to finance MitoCareX’s operations through public or private equity or debt financings or other capital sources of MitoCareX, including potential collaborations, licenses, and other similar arrangements involving MitoCareX. Such transactions could include the issuance of new equity interests in MitoCareX to third parties, which may dilute the Company’s ownership and/or the value of its investment in MitoCareX.
Its future capital requirements will depend on many factors, including, but not limited to:
● the initiation, type, number, scope, progress, expansions, results, costs, and timing of preclinical studies and clinical trials of ACSMT that MitoCareX is pursuing or may choose to pursue in the future, including the costs of any third-party products used as combination agents in its clinical trials; the costs and timing of manufacturing for ACSMT, including commercial manufacturing at sufficient scale, if any ACSMT is approved;
● the costs, timing, and outcome of regulatory meetings and reviews of ACSMT;
Management's Discussion & Analysis (MD&A)
New heading “Change in fair value of contingent consideration”
New heading “Depreciation and amortization”
New heading “Net Loss from continued operations”
New heading “Net loss from discontinued operations”
Removed heading “MitoCareX Bio Transactions”
Removed heading “Private Placement”
Removed heading “Plantify Debt Settlement”
Removed heading “Credit Facility Agreement”
Removed heading “Revenues and Cost of Revenues”
Removed heading “Selling and Marketing Expenses”
Removed heading “Selling and Marketing Expenses”
Largest changes
“We operate through our two majority-owned Israeli subsidiaries, and one joint venture: (1) Save Foods Ltd., which focuses on post-harvest treatments in fruit and vegetables to control and prevent pathogen contamination, significantly reduce the use of hazardous chemicals and prolong fresh produce’s shelf life. (2) NTWO OFF which offers a pioneering solution to mitigate N2O (nitrous oxide) emissions, a potent greenhouse gas with 265 times the global warming impact of carbon dioxide. …”see in full comparison
“On December 22, 2024, we entered into a loan agreement with MitoCareX and Pure Capital, pursuant to which the Company agreed to loan $250,000 to MitoCareX at an annual interest rate pursuant to Section 3(j) of the Income Tax Ordinance, published by the Israel Tax Authority for loans in US dollars, which is currently the USD exchange rate fluctuation plus 3%, as may be adjusted from time to time. The term of the loan is six months with repayment of principal and accrued interest due at maturity. …”see in full comparison
“On the terms and subject to the conditions set forth in the SF Services Agreement, the consideration to be delivered by Voice Assist to us consists of (i) deferred cash consideration in an aggregate amount of $1,000,000, payable solely from future Voice Assist equity and/or debt financing transactions completed during the five-year period beginning on the execution date of the SF Services Agreement, in installments equal to no less than 5% and no more than 15% of the gross proceeds actually received by Voice Assist in each such financing, with each installment payable within 20 days after …”see in full comparison
“According to the SHA, we will lend €2,300,000 to SBI4 for financing two battery storage projects in Sicily, Italy, with the loan accruing interest at 7% per annum. The SHA includes a right of repurchase for SB if we fail to provide drawdown amounts in accordance with the terms of the SHA. Financing may be sought from Shareholders (as defined in the SHA) if external options are unavailable, with unaccepted portions convertible into equity. …”see in full comparison
“As of December 31, 2025, we had cash and cash equivalents of $3,832,000, as compared to $1,923,000 as of December 31, 2024. As of December 31, 2025, we had a working capital of $4,580,000, as compared to $2,560,000 as of December 31, 2024. The increase in our cash balance is mainly attributable to cash provided by financing activities. During 2025, the Company completed the sale of its NTWO OFF Ltd operations and classified its Save Foods business as held for sale and discontinued operations. …”see in full comparison
Full comparison: every changed paragraph (89)
MitoCareX is a drug discovery company dedicated to the development of cancer therapeutics by targeting the mitochondrial carrier family (SLC25A protein family) with a specific focus on one undisclosed SLC25A protein of interest. The company’s core technology and know-how relate to structural biology combined with computational chemistry – a knowledge that can be utilized for potentially each of the 53 protein members belonging to the SLC25A family (i.e., a platform-based drug discovery company). MitoCareX’s current focus is on Non-Small Cell Lung Cancer (NSCLC) therapeutics however it may consider other oncology and non-oncology indications in the future. MitoCareX’s mission is to be the foremost biopharma company that develops and delivers transformative metabolic-based therapies that improve and extend the lives of patients.
We
develop eco-friendly “green” solutions for the food industry. Our solutions are developed to improve the food safety and
shelf life of fresh produce. We do this by controlling human and plant pathogens, thereby reducing spoilage, and in turn, reducing food
loss.
We
operate through our two majority-owned Israeli subsidiaries, and one joint venture: (1) Save Foods Ltd., which focuses on post-harvest
treatments in fruit and vegetables to control and prevent pathogen contamination, significantly reduce the use of hazardous chemicals
and prolong fresh produce’s shelf life. (2) NTWO OFF which offers a pioneering solution to mitigate N2O (nitrous oxide) emissions,
a potent greenhouse gas with 265 times the global warming impact of carbon dioxide. Through NTWO OFF we aim to promote agricultural practices
that are both environmentally friendly and economically viable and to become a global leader in this field by collaborating with or acquiring
other companies that create innovative solutions and tools to solve other aspects of global warming’s impact of carbon dioxide.(3)
A joint venture with Solterra, which operates in the solar energy section and presents certain investment opportunities in solar PV projects.
Our
solutions are based on our proprietary blend of food acids combined with certain types of oxidizing agent-based sanitizers and in some
cases with fungicides at low concentrations. Our products have a synergistic effect when combined with these oxidizing agent-based sanitizers
and fungicides. Our “green” solutions are capable of cleaning, sanitizing, and controlling pathogens on fresh produce with
the goal of making them safer for human consumption and extending their shelf life by reducing their decay. One of the main advantages
of our products is that our ingredients do not leave any toxicological residues on the fresh produce we treat. In contrast, by forming
a temporary protective shield around the fresh produce we treat, our products make it difficult for pathogens to develop and potentially
provide protection which also reduces cross-contamination.
During 2025, the Company underwent significant changes to its business operations. In April 2025, the Company completed the sale of its NTWO OFF Ltd. operations. In addition, during 2025, the Company classified its Save Foods operations as held for sale and discontinued operations. Accordingly, the results of these operations are presented separately in the consolidated financial statements and are not included in the discussion of continuing operations below.
As a result of these changes, the Company’s consolidated financial statements for the periods presented have been reclassified to conform to the current presentation, and therefore may not be directly comparable to prior periods. Unless otherwise indicated, the discussion below relates to the Company’s continuing operations.
MitoCareX Bio Transactions
On
February 25, 2025, we entered into a securities purchase and exchange agreement (the “SPEA”) with MitoCareX Bio Ltd., a
private company incorporated under the laws of the State of Israel (“MitoCareX”), SciSparc Ltd., a public company
incorporated under the laws of the State of Israel (“SciSparc”), Dr. Alon Silberman (“Alon”) and Prof. Ciro
Leonardo Pierri (together with SciSparc and Alon, the “Sellers”) pursuant to which we will acquire from each of the
Sellers their respective ordinary shares, nominal (par) value NIS 0.01 each, of MitoCareX (the “Ordinary Shares”),
thereby resulting in MitoCareX becoming a wholly-owned subsidiary of N2OFF. The closing of the transactions contemplated under the
SPEA is subject to stockholder approval. Under the SPEA, SciSparc will sell 6,622 Ordinary Shares to us (the “Purchased
Shares”) in consideration for a cash payment of $700,000. We will issue (i) to Alon shares of our common stock representing
15.5% on a fully-diluted basis; (ii) to Ciro representing 7.75% on a fully-diluted basis; and (iii) to SciSparc representing 16.75%
on a fully-diluted basis, (the “SPEA Closing”); and in exchange, each of the Sellers will transfer 100% of their
Ordinary Shares to us (and for SciSparc, such amount of Ordinary Shares that, together with the Purchased Shares, represents 100% of
SciSparc’s holdings in MitoCareX. The Sellers are entitled to additional shares of Common Stock, for no additional
consideration, up to 25% of our issued and outstanding capital stock on a fully-diluted basis calculated as of immediately following
the SPEA Closing in accordance with certain milestones set forth in the agreement. Effective as of the SPEA Closing, the board of
directors of MitoCareX will be reconstituted so as to consist of three directors, all of whom will be appointed by us.
Immediately
prior to the SPEA Closing, Alon will enter into an amended employment agreement (the “Amended CEO Agreement”) with us and
MitoCareX in connection with his employment as the Chief Executive Officer of MitoCareX, which Amended CEO Agreement provides, among other
things, for a grant of restricted stock representing 5% of our capital stock on a fully diluted basis. Such shares will vest quarterly,
in equal installments, for three years, subject to Alon’s continued employment with MitoCareX.
The
Sellers will receive, collectively, 30% of the gross proceeds of each financing transaction closed by us for five years up to
$1,600,000.
We
have committed to an initial investment of $1,000,000 in MitoCareX, less any such amounts previously loaned to MitoCareX pursuant to loan agreements, dated December 22, 2024 and March 12, 2025, among N2OFF, MitoCareX and Pure Capital. and future financing of MitoCareX’s
ongoing research and development subject to our board of directors approval of an operating plan and financial resources necessary to
provide such funding.
Alon,
the chief executive officer of MitoCareX is the brother of Kfir Silberman, the owner of Pure Capital, a stockholder and lender of our
company, and each of Amitay Weiss and Liat Sidi, members of our board of directors, also serve as board members of SciSparc.
SolterraSave
Foods TransactionsTransaction
On January 13, 2026, we entered into the SF Agreement with Voice Assist. Pursuant to the SF Agreement, at the Closing we transferred to Voice Assist all of the ordinary shares of Save Foods owned by us, representing approximately 98% of the issued and outstanding share capital of Save Foods (the “SF Shares”), free and clear of any encumbrances. The SF Agreement contains customary representations, warranties, covenants and closing conditions for transactions of this type.
On the terms and subject to the conditions set forth in the SF Agreement, the consideration delivered by Voice Assist to us for the SF Shares consist of the issuance at Closing to us of that number of shares of common stock of Voice Assist, par value $0.001 per share, that represented 19.99% of Voice Assist shares of common stock on a fully-diluted basis, calculated as of immediately following the closing of the SF Agreement.
We also entered into a Services Agreement with Voice Assist (the “SF Services Agreement”), pursuant to which we provide non-exclusive general advisory, support, collaboration and related services to Voice Assist from time to time.
On the terms and subject to the conditions set forth in the SF Services Agreement, the consideration to be delivered by Voice Assist to us consists of (i) deferred cash consideration in an aggregate amount of $1,000,000, payable solely from future Voice Assist equity and/or debt financing transactions completed during the five-year period beginning on the execution date of the SF Services Agreement, in installments equal to no less than 5% and no more than 15% of the gross proceeds actually received by Voice Assist in each such financing, with each installment payable within 20 days after Voice Assist’s receipt of such proceeds, subject to an aggregate cap of $1,000,000; (ii) ongoing royalty consideration equal to 75% of the gross profit generated from “New Future Projects” (as defined in the Services Agreement) during the first three years following such execution date, 15% of such gross profit generated during years four through ten following such date, and 5% thereafter, in each case calculated as set forth in the SF Services Agreement; and (iii) an amount equal to 75% of any “Ecolab Gross Proceeds” (as defined in the Services Agreement) actually received by Voice Assist, Save Foods or their respective affiliates in respect of the “Ecolab Claim,” in each case as defined and on the terms set forth in the SF Services Agreement.
The SF Services Agreement will remain in effect through calendar year 2026, and we may, in our sole discretion, extend the SF Services Agreement from time to time until we have received the full amount of the consideration payable to us under the SF Services Agreement.
On February 24, 2025, we entered into a shareholder’s agreement with Solterra Brand Services Italy SRL, an
Italian company (“SB”), and its wholly owned Israeli subsidiary, SB Impact 4 Ltd. (“SBI4” and the “SHA”,
respectively) pursuant to which our newly formed wholly-owned subsidiary, NITO Renewable will acquire 70% of SBI4’s shares from
SB in order to finance two battery storage projects in Sicily, Italy.
According to the SHA, we will lend €2,300,000 to
SBI4 for financing two battery storage projects in Sicily, Italy, with the loan accruing interest at 7% per annum. The SHA includes a
right of repurchase for SB if we fail to provide drawdown amounts in accordance with the terms of the SHA. Financing may be sought from
Shareholders (as defined in the SHA) if external options are unavailable, with unaccepted portions convertible into equity. Profits from
the sales of PV Projects will be distributed based on share ownership, with adjustments as follows: if the selling price per megawatt
(“MW”) (i) does not exceed €30,000, each party will receive profits according to its pro-rata share ownership of SBI4;
(ii) exceeds €30,000 up to €60,000 per MW, SB will receive 40% of the profit (10% above its pro-rata share) and we will receive
60% of the profit; and (iii) exceeds €60,000 per MW, SB will receive 50% of the net profit (20% above its pro-rata share) and we
will receive 50% of the net profit. Share transfer restrictions apply, requiring consent and adherence to the terms of the SHA. A party
will cease to be a party to the SHA if its shareholding drops below 10%.
On February 10, 2025, we established NITO Renewable Energy, Inc., in the State of Nevada (“NITO Renewable”)
for the purposes of managing and facilitating our investment opportunities in the solar energy sector.
On
November 27, 2024, we acquired 100,000 shares of Solterra Energy Ltd. (“Solterra Energy”) for NIS 300,000 (approximately
$82,000). Subsequently, on December 31, 2024, we acquired an additional 167,000 shares of Solterra Energy for NIS 501,000
(approximately $137,000), which resulted in us owning less than 5% of the outstanding shares of Solterra Energy.
There were no issuances of equity securities to directors during the year ended December 31, 2025.
On February 9, 2026, we issued 116,286 shares of common stock to the chairman of the board of directors.
Loan Agreement
On
December 22, 2024, we entered into a loan agreement with MitoCareX and Pure Capital, pursuant to which the Company agreed to loan
$250,000 to MitoCareX at an annual interest rate pursuant to Section 3(j) of the Income Tax Ordinance, published by the Israel Tax
Authority for loans in US dollars, which is currently the USD exchange rate fluctuation plus 3%, as may be adjusted from time to
time. The term of the loan is six months with repayment of principal and accrued interest due at maturity. In the event of a
transaction whereby MitoCareX becomes a subsidiary of the Company, any amount outstanding under the loan will be deducted from any
future amount allocated by us to MitoCareX during the first year following a transaction. Pure Capital has agreed to guarantee the
repayment of the loan by MitoCareX.
On March
12, 2025, we entered into a loan agreement with MitoCareX for an additional $250,000 under the same terms as prior loan agreement.
Private Placement
On December
10, 2024, we entered into a securities purchase agreement (the “Purchase Agreement”) with each of the Selling Stockholders
for aggregate gross proceeds of approximately $1,500,000 and agreed to issue an aggregate of 6,250,000 Units and/or pre-funded units (collectively,
the “Units”) at a purchase price of $0.24 per unit (less $0.00001 per pre-funded unit). Each Unit consists of (i) one share
of common stock and/or one pre-funded warrant to purchase one share of common stock (the “Pre-Funded Warrants”), and (ii)
a one and a half warrant to purchase one share of common stock (the “Common Warrant” and together with the Pre-Funded Warrants,
the “Warrants”).
The
Pre-Funded Warrants are immediately exercisable at an exercise price of $0.00001 per share of common stock and will not expire until exercised
in full. The Common Warrants have a five-year term, are immediately exercisable and have an exercise price of $0.24, subject to certain
anti-dilution and stock combination event protections. The Warrants may be exercised on a cashless basis.
The Warrants
may not be exercised if such exercise would result in an investor beneficially owning in excess 4.99% of the Company’s outstanding
capital stock (the “Beneficial Ownership Limitation”). The exercise price of the Warrants and number of shares issuable upon
the Warrants (the “Warrant Shares”) are subject to adjustments upon the issuance of certain common stock, options, convertible
securities and stock combination events.
On December
11, 2024, the Common Warrant was amended to provide for a floor price if the anti-dilution provisions of the Common Warrant are triggered.
The floor price is not less than $0.048 (20% of $0.24), subject to customary adjustments for stock splits and similar transactions. If
the exercise price is reduced as a result of a dilutive issuance, then the new exercise price will be reduced to the floor price and the
number of Warrant Shares will be proportionately increased.
On January
2, 2025, we consummated the private placement transactions contemplated by the securities purchase agreement, dated December 10, 2024
and issued 1,704,116 shares; pre-funded warrants to purchase 4,545,884 shares; and warrants to purchase 9,375,000 shares of our common
stock. We received gross proceeds of $1,500,000 as a result of such issuances.
On March
19, 2025, we amended the Purchase Agreement to increase the Beneficial Ownership Limitation from 4.99% to 9.99% of our outstanding
common stock.
Plantify Debt Settlement
On November
15, 2024, we entered into a debt settlement agreement (the “Settlement Agreement”) with Plantify pursuant to which Plantify
issued 2,420,848 of its common shares (the “Settlement Shares”) to us at CDN$0.848 per share in full payment of debt owed
to the Company in aggregate amount of CDN$2,053,000 (the “Debt”). The Debt consisted of (i) CDN$1,691,000, representing the
principal and accrued interest on a convertible debenture which matured on October 4, 2024 and (ii) US$258,000 representing draws against
a line of credit which we had made available to Plantify of up to $250,000 in April 2024. The closing of the Settlement Agreement occurred
on December 5, 2024 upon the approval by the TSX Venture Exchange of the issuance (the “Closing Date”). On the Closing Date,
Plantify issued the Settlement Shares to us and we released and discharged Plantify from all claims, demands, obligations and damages
arising under or related to the Debt and released the shares of Plantify’s subsidiary, Peas of Bean Ltd., the collateral securing
the convertible debenture.
As a
result of the issuance of the Settlement Shares, we owned approximately 65% of the outstanding shares of Plantify for a limited period
from December 5, 2024 until December 20, 2024. On December 20, 2024, Plantify notified us that it had issued its common shares in a private
placement offering which resulted in us owning approximately 27% of the outstanding shares of Plantify.
On January
12, 2025, Plantify informed us that it issued additional shares to an additional lender as a debt settlement. As a result of such issuance,
our share ownership of Plantify decreased to approximately 25%.
Amended Bylaws
Effective
November 11, 2024, our board of directors approved and adopted amended and restated our bylaws to change the quorum requirement from a
majority of the shares entitled to vote at a meeting of stockholders to 33.33% of the voting power entitled to vote at a stockholder meeting.
Credit Facility Agreement
On October 1, 2024, we entered
into a facility agreement (the “Facility Agreement”) with Pure Capital for financing of up to EUR 6,000,000 (the “Credit
Facility”), EUR 2,000,000 of which may be used to finance one project in Germany, and the remaining EUR 4,000,000 for any other
projects subject to pre-approval by Pure Capital. Under the Facility Agreement, we agreed to issue the Lender a five-year warrant (the
“Facility Warrant”) to purchase 1,850,000 shares of common stock (the “Facility Warrant Shares”), with an exercise
price of $1.00 per share. Such warrant may not be exercised by the Lender if such exercise would result in the Lender beneficially owning
in excess of 4.99% of our outstanding shares of common stock. The Facility Warrant Shares are immediately exercisable.
Notwithstanding that the Facility
Warrant Shares are immediately exercisable, Pure Capital has agreed, pursuant to a waiver agreement with us, dated December 5, 2024, (“Waiver
Agreement”) not to exercise the Facility Warrant until we obtain stockholder approval.
Revenues
and Cost of Revenues
Our
total revenue consists of products and our cost of revenues consists of cost of products.
The
following table discloses the breakdown of revenues and costs of revenues:
Our
current operating expenses consist of threefour components - research and development expenses, sellinggeneral and marketing expenses and general
and administrative expenses.expenses, change
in fair value of contingent consideration and depreciation and amortization.
We
implemented certain cost reduction measures in 2023, including, the reduction of our research and development expenses, as we decided
to focus on marketing and sales to try to materialize the efforts of our pilots conducted during 2022 and 2023. Following our August
29, 2023 Exchange Agreement with Yaaran Investment Ltd. we recorded IPR&D costs associated with such transaction and were committed
to invest research and development expenses under the said Exchange Agreement, for further information, see Research and Development
Expenses below.
Selling
and Marketing Expenses
Selling
and marketing expenses consist primarily of salaries and related expenses and other expenses.
The
following table sets forth the breakdown of selling and marketing expenses:
Revenues
Revenues
for the year ended December 31, 2024 were $210,000, a decrease of $53,000, or 20%, compared to revenues of $263,000 for the year ended
December 31, 2023. The decrease is mainly a result of a decrease in our sales in Mexico.
Cost
of Sales
Cost
of sales consists primarily of salaries, materials, and overhead costs of manufacturing our products. Cost of sales for the year ended
December 31, 2024 was $165,000, an increase of $110,000, or 200%, compared to total cost of sales of $55,000 for the year ended December
31, 2023. The increase is mainly a result of inventory write-off in South Africa and Turkey and unexpected surge in material consumption
due to temporary malfunction in our US client.
Gross
Profit
Gross
profit for the year ended December 31, 2024 was $45,000, a decrease of $163,000, or 78%, compared to gross profit of $208,000 for the
year ended December 31, 2023. The decrease is mainly a result of the increase in cost of sales .
Research and development expenses consist of Salaries and related expenses, service providers’ costs, related materials and overhead expenses. Research and development expenses for the year ended December 31, 2025 were $179,000, compared to no research and development expenses for the year ended December 31, 2024. The increase was attributable to research and development activities following the acquisition of MitoCareX in October 2025, including personnel-related expenses and costs associated with its ongoing development programs.
Research
and development expenses consist of consulting fees, service providers’ costs, related materials and overhead expenses. Research
and development expenses for the year ended December 31, 2024 were $369,000, a decrease of $1,569,000, or 81%, compared to research and
development expenses of $1,938,000 for the year ended December 31, 2023. The decrease is mainly attributable to a decrease in Save Foods
Ltd.’s expenses as a result of the implementation of certain cost reduction measures, including a reduction in Save Foods Ltd.’s
research and development budget in light of prevailing macroeconomic conditions and the shift of our focus to the commercialization of
our solutions and converting recently completed pilots into paying customers. Additionally, certain results of our operations relating
to Save Foods Ltd., were offset by an increase in professional fees associated with NTWO OFF Ltd.’s research and development activities.
Selling
and Marketing Expenses
What changed in the latest 10-Q
Risk Factors
We are a smaller reporting company, as defined by Rule 12b-2 of the Exchange Act, and are not required to provide the information under this item.
No wording changes found in this section.
Full comparison: every changed paragraph (0)
Management's Discussion & Analysis (MD&A)
New heading “All information in this Quarterly Report relating to shares or price per share reflects the 1-for-35 reverse stock split effected by us on September 22, 2025 and the 1-for-7 reverse stock split effected by us on April 8, 2026.”
New heading “Amendment to Credit Facility Agreement”
New heading “Registered Direct Offerings and Concurrent Private Placements”
New heading “Change in Independent Registered Public Accounting Firm”
New heading “Depreciation and amortization”
New heading “Financing expenses, Net”
New heading “Net Loss from continuing operations”
New heading “Net gain (loss) from discontinued operations”
New heading “Six months ended June 30, 2026 compared to six months ended June 30, 2025”
New heading “Research and Development Expenses”
New heading “General and Administrative Expenses”
New heading “Change in fair value of contingent consideration”
Removed heading “Special General Meeting”
Removed heading “Save Foods Transaction”
Removed heading “Issuances of common stock”
Removed heading “Name Change and the Symbol Change”
Removed heading “Reverse Stock Split”
Largest changes
“All information in this Quarterly Report relating to shares or price per share reflects the 1-for-35 reverse stock split effected by us on September 22, 2025 and the 1-for-7 reverse stock split effected by us on April 8, 2026.”see in full comparison
“Six months ended June 30, 2026 compared to six months ended June 30, 2025”see in full comparison
“On the terms and subject to the conditions set forth in the SF Services Agreement, the consideration to be delivered by Voice Assist to us consists of (i) deferred cash consideration in an aggregate amount of $1,000,000, payable solely from future Voice Assist equity and/or debt financing transactions completed during the five-year period beginning on the execution date of the SF Services Agreement, in installments equal to no less than 5% and no more than 15% of the gross proceeds actually received by Voice Assist in each such financing, with each installment payable within 20 days after …”see in full comparison
Full comparison: every changed paragraph (82)
All information in this Quarterly Report relating to shares or price per share reflects the 1-for-35 reverse stock split effected by us on September 22, 2025 and the 1-for-7 reverse stock split effected by us on April 8, 2026.
MitoCareX,
which has been our wholly owned subsidiary since October 2025, develops and advances targeted small-molecule therapeutics for oncologydiverse types of indications
by focusing on thetransport mitochondrialproteins SLC25A(i.e., proteintransporters). family.MitoCareX MitoCareX’sdeveloped solutionstechnologies that are designed to inhibitinteract specificwith SLC25A mitochondrialtransporters
carrier proteins that play a key role in cellular energy metabolism, thereby potentially disrupting cancerthe celldisease. growthMitoCareX androutinely survival. We are currently
focused on Non-Small Cell Lung Cancer (NSCLC) and utilizeutilizes structural
biology in combination with computational chemistry to discover, design and develop drug
candidates that selectively bindinteract towith our SLC25Aits
protein targets of interest. OurMitoCareX approach leverages oura proprietary MITOLINE™ algorithm,
which enables the reliable generation
of 3D molecular structural models acrossof allMitoCareX’s 53protein human SLC25A proteinstargets and allows for large-scale
virtual screening of moleculescampaigns against
these targets. MITOLINE™ provides a platform-level capabilitystarting point to identifyenable new mitochondrial
carrier targetsmodelling and further allows to develop novel therapeutics in areas where no FDA-approved SLC25A-directed therapies currently exist. therapeutics.
A key advantage
of ourMitoCareX platform is its ability to address the historical lack of experimental structural data that has limited
drug discovery efforts targeting SLC25A
proteins,MitoCareX’s proteins of interest, thereby expanding the druggable target space within mitochondrial biology.space. By enabling rational,
structure-guided inhibitor
discovery at scale, MitoCareX’s solutions are designed to unlock new treatment opportunities in NSCLC and potentially other oncology
and disease indications associated with mitochondrial dysfunction.opportunities.
We
collaborate with Solterra Renewable Energy Ltd., an Israeli corporation (“Solterra”) and a former wholly-owned subsidiary
of Solterra
Energy Ltd., an Israeli corporationpublic corporation, listed on the Tel Aviv Stock Exchange (“Solterra Energy”), which
operates in the solar energy sector and presents certain investment
opportunities in solar photovoltaic (“PV”) projects.
Solterra engages in the development of renewable energy projects through
its subsidiaries. Currently, operations are conducted in Italy,
Poland, and Germany, with potential expansion to additional countries.
Our subsidiary, NITO Renewable, was established in February 2025
in the State of Nevada and has a 70% interest in the joint venture in
Italy. Solterra’s business strategy primarily involves selling
renewable energy projects to third parties at various stages of
development, from the initial land identification and project advancement
through construction, operation, or sale to a third party.
Currently, most projects are expected to be sold at various development stages,
with the possibility of a larger portion of projects
being held long-term for operation by Solterra in the future. In July 2026, Solterra
Energy completed the sale of 100% of the issued share capital of Solterra to Sunflower Sustainable Investments Ltd., an Israeli public
corporation listed on the Tel Aviv Stock Exchange. We currently intend to continue to collaborate with Solterra as Solterra
surveys the
European solar energy market for additional projects.
During
2025, the Company underwent significant changes to its business operations. In April 2025, the Company completed the sale of its NTWO
OFF Ltd. operations. In addition, during 2025, the Company classified itsthe operations of Save Foods operationsLtd., our former 98.48% owned subsidiary
(“Save Foods”), as held for sale and discontinued operations.
Accordingly, the results of these operations are presented
separately in the consolidated financial statements and are not included in
the discussion of continuing operations below.
Amendment to Credit Facility Agreement
On April 30, 2026, we held a special general meeting of stockholders (the “Special Meeting”) to approve, among others, an amendment to a facility agreement (the “Original Facility Agreement”) with L.I.A. Pure Capital Ltd. (the “Lender”) for financing of up to EUR 6,000,000 (the “Original Credit Facility”), EUR 2,000,000 of which may be used to finance one project in Germany, and the remaining EUR 4,000,000 for other projects subject to the Lender’s pre-approval.
In connection with the Original Facility Agreement, we issued to the Lender a five-year warrant (the “Warrant”) to purchase 1,850,000 shares of our common stock (the “Warrant Shares”) at an exercise price of $1.00 per share, subject to customary anti-dilution adjustments.
Our stockholders previously approved the issuance of the Warrant Shares in accordance with Nasdaq Listing Rule 5635(d).
Following the approval of our stockholders at the Special Meeting, on May 27, 2026, we and the Lender released from escrow the signatures to the amended and restated facility agreement (the “Amended and Restated Facility Agreement”), which, among other things: (i) increases the total amount available under the credit facility from EUR 6,000,000 to EUR 10,000,000; and (ii) amends certain provisions relating to the Warrants, such that, following proportionate adjustments to the number of Warrant Shares and the exercise price as a result of the Company’s reverse stock splits, the Warrant was reset to entitle the Lender to purchase 1,850,000 shares of our common stock at an exercise price of $1.00 per share and include an anti-dilution adjustment mechanism, including adding a “price maintenance” provision to the Warrant’s anti-dilution adjustment mechanism. This provision is intended to preserve the economic value of the Warrant and provides that, upon certain future issuances of our securities at prices below the then-current exercise price of the Warrant, adjustments may be made to reduce the Warrant exercise price; and/or increase the number of Warrant Shares issuable upon exercise.
Except as modified, the principal economic terms of the credit facility, including interest rate, repayment structure, drawdown period, and general warrant terms, remain substantially consistent with the Original Facility Agreement.
Registered Direct Offerings and Concurrent Private Placements
On June 12, 2026, we entered into a securities purchase agreement with certain investors pursuant to which we issued and sold in a registered direct offering, an aggregate of 311,876 shares of our common stock at a purchase price of $4.008 per share (the “First June 2026 Registered Direct Offering”).
In a concurrent private placement (the First June 2026 Private Placement and together with the First June 2026 Registered Direct Offering, the “First June 2026 Offerings”), we also issued to the same investors an aggregate of 311,876 common warrants to purchase up to 311,876 shares of our common stock. The common warrants are exercisable upon issuance at an exercise price of $4.008 per share, subject to adjustment as set forth therein, and have a 5-year term from the issuance date. The common warrants may be exercised on a cashless basis if there is no effective registration statement registering the shares of common stock underlying such common warrants. A holder of the common warrants will not have the right to exercise any portion of its common warrants if the holder (together with such holder’s affiliates, and any persons acting as a group together with such holder or any of such holder’s affiliates or any other persons whose beneficial ownership of shares of our common stock would be aggregated with the holder’s or any of the holder’s affiliates), would beneficially own shares of our common stock in excess of 4.99% of the number of shares of common stock outstanding immediately after giving effect to such exercise.
Aggregate gross proceeds in respect of the First June 2026 Offerings were approximately $1.25 million, before deducting offering expenses payable by us. The First June 2026 Offerings closed on June 15, 2026.
On June 22, 2026, we entered into a securities purchase agreement with certain investors pursuant to which we issued and sold in a registered direct offering an aggregate of 410,998 shares of our common stock at a purchase price of $7.056 per share. (the “Second June 2026 Registered Direct Offering”).
In a concurrent private placement (the “Second June 2026 Private Placement” and together with the Second June 2026 Registered Direct Offering, the “Second June 2026 Offerings”), we also issued to the same investors an aggregate of 410,998 common warrants to purchase up to 410,998 shares of our common stock. The common warrants are exercisable upon issuance at an exercise price of $ 7.056 per share, subject to adjustment as set forth therein, and have a 5-year term from the issuance date. The common warrants may be exercised on a cashless basis if there is no effective registration statement registering the shares of common stock underlying such common warrants. A holder of the common warrants will not have the right to exercise any portion of its common warrants if the holder (together with such holder’s affiliates, and any persons acting as a group together with such holder or any of such holder’s affiliates or any other persons whose beneficial ownership of shares of our common stock would be aggregated with the holder’s or any of the holder’s affiliates), would beneficially own shares of our common stock in excess of 4.99% of the number of shares of common stock outstanding immediately after giving effect to such exercise.
Aggregate gross proceeds in respect of the Second June 2026 Offerings were approximately $2.9 million, before deducting offering expenses payable by us. The Second June 2026 Offerings closed on June 24, 2026.
Change in Independent Registered Public Accounting Firm
On August 6, 2026, our board of directors (“the Board”) and the audit committee of the Board approved (i) the dismissal of Somekh Chaikin, a member firm of KPMG International, as the Company’s independent registered public accounting firm and (ii) the appointment of Brightman Almagor Zohar & Co., a firm in the Deloitte Global Network, as the Company’s new independent registered public accounting firm for the fiscal year ending December 31, 2026.
Special
General Meeting
On
April 30, 2026, we held a special general meeting of stockholders (the “Special General Meeting”). A total of 3,129,968 shares
of common stock, representing approximately 61.23% of the shares outstanding and entitled to vote, were present in person or represented
by proxy, constituting a quorum.
At
the Special General Meeting, stockholders considered and approved the following proposals: (i) Proposal No. 1, to approve the amendment
to our Articles of Incorporation, as amended (the “Reverse Split Amendment”), implementing one or more reverse stock splits
of the issued and outstanding shares of our common stock (the “Reverse Stock Split”) at a ratio of not less than 1-for-2
and not more than 1-for-500 (the “Reverse Split Range”), and to grant our board of directors (the “Board”) the
discretionary authority to determine the exact ratio of the Reverse Stock Split within the Reverse Split Range and by such number of
increments, and to effect the Reverse Split Amendment at such times and dates, if at all, as to be determined by the Board in its sole
discretion (the “Reverse Stock Split Proposal”). (ii) Proposal No. 2, to approve the
issuance of securities in one or more non-public offerings where the maximum discount at which securities will be offered will be equivalent
to a discount of 20% below the market price of our common stock, as required by and in accordance
with Nasdaq Marketplace Rule 5635(d) (the “Equity Issuance Proposal”). (iii) Proposal No. 3, to approve,
for Nasdaq Marketplace Rule 5635(d) purposes, the potential issuance of shares of common stock upon exercise of warrants that may be
issued under an amendment to our facility agreement with L.I.A. Pure Capital Ltd. (the “Facility
Amendment Proposal”).(iv) Proposal No. 4, to approve the authorization of an adjournment
of the Special General Meeting to a later date or dates, if necessary, to solicit additional
proxies if there are not sufficient votes in favor of the Reverse Stock Split Proposal, the Equity Issuance Proposal, or the Facility
Amendment Proposal.
Save
Foods Transaction
On
January 13, 2026, we entered into the SF Agreement with Voice Assist. Pursuant to the SF Agreement, at the Closing we transferred to
Voice Assist all of the ordinary shares of Save Foods owned by us, representing approximately 98% of the issued and outstanding share
capital of Save Foods (the “SF Shares”), free and clear of any encumbrances. The SF Agreement contains customary representations,
warranties, covenants and closing conditions for transactions of this type.
On
the terms and subject to the conditions set forth in the SF Agreement, the consideration delivered by Voice Assist to us for the SF Shares
consist of the issuance at Closing to us of that number of shares of common stock of Voice Assist, par value $0.001 per share, that represented
19.99% of Voice Assist shares of common stock on a fully-diluted basis, calculated as of immediately following the closing of the SF
Agreement.
We
also entered into a Services Agreement with Voice Assist (the “SF Services Agreement”), pursuant to which we provide non-exclusive
general advisory, support, collaboration and related services to Voice Assist from time to time.
On
the terms and subject to the conditions set forth in the SF Services Agreement, the consideration to be delivered by Voice Assist to
us consists of (i) deferred cash consideration in an aggregate amount of $1,000,000, payable solely from future Voice Assist equity and/or
debt financing transactions completed during the five-year period beginning on the execution date of the SF Services Agreement, in installments
equal to no less than 5% and no more than 15% of the gross proceeds actually received by Voice Assist in each such financing, with each
installment payable within 20 days after Voice Assist’s receipt of such proceeds, subject to an aggregate cap of $1,000,000; (ii)
ongoing royalty consideration equal to 75% of the gross profit generated from “New Future Projects” (as defined in the Services
Agreement) during the first three years following such execution date, 15% of such gross profit generated during years four through ten
following such date, and 5% thereafter, in each case calculated as set forth in the SF Services Agreement; and (iii) an amount equal
to 75% of any “Ecolab Gross Proceeds” (as defined in the Services Agreement) actually received by Voice Assist, Save Foods
or their respective affiliates in respect of the “Ecolab Claim,” in each case as defined and on the terms set forth in the
SF Services Agreement.
The
SF Services Agreement will remain in effect through calendar year 2026, and we may, in our sole discretion, extend the SF Services Agreement
from time to time until we have received the full amount of the consideration payable to us under the SF Services Agreement.
Issuances
of common stock
On
January 8, 2026, we issued 5,000 shares of common stock pursuant to a new consulting agreement to a consultant in consideration of investor
relations services provided to us.
On
January 22, 2026, we issued 198,172 shares of common stock to YA II PN, Ltd., pursuant to the terms of the Standby Equity Purchase Agreement
dated December 22, 2023 for net proceeds of $2,896.
On
February 9, 2026, our Board approved the issuance of an equity grant to executive officers and consultant of an aggregate of 28,572 shares
of common stock.
On
February 9, 2026, we issued 16,613 shares of common stock to the chairman of the Board.
On
February 23, 2026, we issued 85,716 shares of common stock to consultants in consideration of various investor relations and business
development services provided to us.
Name
Change and the Symbol Change
On
January 26, 2026, our Board approved our name change to “Nexentis Technologies Inc.” which became effective on The Nasdaq
Capital Market on February 26, 2026. Our common stock was traded on the Nasdaq Capital Market under the symbol “NITO” until
February 25, 2026. On February 26, 2026, in connection with our name change on February 26, 2026, our stock began trading under the symbol
“NXTS”.
Reverse
Stock Split
On
September 25, 2025, at the special meeting of stockholders of the Company held on said date, the stockholders approved a proposal authorizing
our Board of directors, in its sole discretion, to amend our Amended and Restated Certificate of Incorporation, at any time within one
year after stockholder approval is obtained, to effect a reverse stock split of the issued and outstanding shares of our common stock,
$0.0001 par value per share, by a ratio of no less than 1-for-2 and no more than 1-for-150, with the exact split ratio to be determined
by the Board in its sole discretion without further approval or authorization of our stockholders. After the special meeting, the Board
determined that it is in the best interests of the Company and its stockholders to effectuate a reverse stock split of our common stock
at a ratio of one-for-seven (1-for-7) (the “April 2026 Reverse Stock Split”). On April 8, 2026, our common stock began trading
on the Nasdaq Capital Market on the post-April 2026 Reverse Stock Split basis. The April 2026 Reverse Stock Split was implemented to
increase the per share price and bid price of the Company’s common stock to regain compliance with the continued listing requirements
of Nasdaq and make the common stock more attractive to certain institutional investors.
As
a result of the April 2026 Reverse Stock Split, every seven (7) shares of issued and outstanding common stock automatically combined
into one (1) issued and outstanding share of Common Stock, without any change in the par value per share. No fractional shares were issued
as a result of the April 2026 Reverse Stock Split. Any fractional shares that would otherwise have resulted from the April 2026 Reverse
Stock Split were rounded up to the next whole number.
All
share, stock option, and per share information presented in these consolidated financial statements have been retroactively adjusted
to reflect the April 2026 Reverse Stock Split.
Three
months ended MarchJune 31,30, 2026 compared to three months ended MarchJune 31,30, 2025
Research
and development expenses consist of Salariessalaries and related expenses, service providers’ costs, related materials and overhead expenses.
Research and development expenses for the three months ended MarchJune 31,30, 2026 were $275,000,$373,000, compared to no research and development expenses
for the three months ended MarchJune 31,30, 2025. The increase was attributable to research and development activities following the acquisition
of MitoCareX in October 2025, including personnel-related expenses and costs associated with its ongoing development programs.
General
and administrative expenses consisted primarily of professional services, salaries and related expenses including share based compensation
and other non-personnel related expenses, including legal expenses and directors and officers insurance costs. General and administrative
expenses for the three months ended MarchJune 31,30, 2026 were $1,899,000,$1,257,000, ana increasedecrease of $1,396,000,$1,370,000, or 278%,52%, compared to general and administrative
expenses of $503,000$2,627,000 for the three months ended MarchJune 31,30, 2025. The increasedecrease was primarily attributable to higherdecrease of share-based compensation
to our employees and service providers, aspartially welloffset asby increasedan increase of professional services and legal expenses, partially offset by a decrease
of insurance costs.expenses.
Change
in fair value of contingent consideration for the three months ended MarchJune 31,30, 2026 was a gainnet loss of $343,000.$139,000. The gain is related to the
contingent cash and
equity consideration was recognized in connection with the acquisition of MitoCareX in October 2025.2025 The fair value of
the contingent considerationand is remeasured at fair value at
each reporting date, andwith changes in fair value are recognized in the statement of operations.
The gainnet wasloss primarily attributableresulted to a decrease infrom the estimated fair value remeasurement
of the contingent consideration,cash mainlyconsideration dueupon tobecoming certain
cashfixed and equity consideration no longer being considered contingent. Specifically,payable following the Company’s financing activities, after which
certain cash consideration became payable andit was reclassified outto ofaccrued contingentexpenses. consideration.This Inloss addition,was followingpartially MitoCareX’s
achievementoffset by a gain from the remeasurement of the first milestone, the relatedcontingent equity considerationconsideration,
which becamecontinues payableto andbe wasmeasured no longer included in theat fair value measurement
of contingent consideration.value.
Depreciation and amortization
Depreciation and amortization for the three months ended June 30, 2026 was $106,000, compared to $0 for the three months ended June 30, 2025. The increase was attributable to the amortization of intangible assets recognized in connection with the acquisition of MitoCareX in October 2025 as part of the purchase price allocation.
Financing expenses, Net
Financing expenses, net for the three months ended June 30, 2026 was $8,839,000, an increase of $7,605,000 or 616%, compared to financing expenses, net of $1,234,000 for the three months ended June 30, 2025. The increase was primarily attributable to expenses resulting from changes in the fair value of the warrant liabilities associated with the amendment to the Credit Facility Agreement and the day-one losses recognized upon the issuance of the First PIPE Warrants and the Second PIPE Warrants in June 2026. These expenses were partially offset by gains from the subsequent remeasurement of the PIPE warrant liabilities.
Income taxes
Income tax benefit for the three months ended June 30, 2026 was $23,000. The tax benefit is primarily attributable to a reduction in deferred tax liabilities, and does not reflect taxable income generated from operations. The decrease in deferred tax liabilities was primarily related to the amortization of intangible assets recognized in connection with the acquisition of MitoCareX, which resulted in a corresponding income tax benefit.
Net Loss from continuing operations
Net loss from continuing operations for the three months ended June 30, 2026, was $11,160,000, compared to $4,387,000 for the three months ended June 30, 2025, an increase of $6,773,000, or 154%. The increase was primarily attributable to higher financing expenses, net, as discussed above.
Net gain (loss) from discontinued operations
No gain or loss from discontinued operations was recognized for the three months ended June 30, 2026, as the sale of the Company’s former Save Foods business was completed on March 15, 2026. This compares to a net loss from discontinued operations of $121,000 for the three months ended June 30, 2025, which reflected the operating results of the former Save Foods business.
Total net loss
As a result of the foregoing, our total net loss for the three months ended June 30, 2026 was $11,160,000 compared to $4,508,000 for the three months ended June 30, 2025, an increase of $6,652,000, or 148%.
Six months ended June 30, 2026 compared to six months ended June 30, 2025
Research and Development Expenses
Research and development expenses consist of salaries and related expenses, service providers’ costs, related materials and overhead expenses. Research and development expenses for the six months ended June 30, 2026 were $648,000, compared to no research and development expenses for the six months ended June 30, 2025. The increase was attributable to research and development activities following the acquisition of MitoCareX in October 2025, including personnel-related expenses and costs associated with its ongoing development programs.
General and Administrative Expenses
NXTS insider buying and selling (Form 4)
Since 2026-04-11, insiders reported open-market purchases in 0 Form 4 filings and open-market sales in 0 filings. Totals add up every open-market (code P and S) line in those filings, using the prices reported in the filings. Awards, option exercises, tax withholding and gifts are listed below but not counted.
No Form 4 stock transactions in this period.
Well-known investors holding NXTS (13F)
None of the 59 investors we track reported a position in their latest 13F.