STOCK TITAN

Scinai Announces Completion of Acquisition of Recipharm Israel Ltd. and Strategic Commercial Collaboration with Recipharm

Rhea-AI Impact
(Moderate)
Rhea-AI Sentiment
(Positive)
Tags
partnership acquisition

Scinai (NASDAQ: SCNI) completed the acquisition of 100% of Recipharm Israel Ltd., adding a cGMP Yavne manufacturing site and expanding Scinai's CDMO footprint and technical scope.

The companies also signed a long-term commercial collaboration granting Scinai preferred early-stage status and access to Recipharm's global manufacturing network under predefined terms, plus a Master Quality Agreement and Tech Transfer Framework to streamline program transitions.

Loading...
Loading translation...

Positive

  • Acquisition of 100% of Recipharm Israel Ltd., adding a cGMP Yavne site
  • Expanded CDMO services to include recombinant proteins, small molecules, peptides, antibodies, oligonucleotides
  • Preferred partner status for early-stage work and access to Recipharm's global manufacturing network
  • Master Quality & Tech Transfer framework to enable smoother program transitions
  • Referral economics allow Scinai to participate economically in later-stage and commercial success

Negative

  • Financial terms of the share purchase agreement remain confidential
  • Late-stage supply through Recipharm is subject to capacity and technical suitability

Key Figures

Stake acquired: 100% of shares
1 metrics
Stake acquired 100% of shares Acquisition of Recipharm Israel Ltd.

Market Reality Check

Price: $0.7444 Vol: Volume 13,596 is 0.25x th...
low vol
$0.7444 Last Close
Volume Volume 13,596 is 0.25x the 20-day average 55,266, suggesting limited pre-news positioning. low
Technical Shares at 0.7444, trading below the 200-day MA of 1.6 and far under the 6.18 52-week high.

Peers on Argus

Momentum scanner shows 2 peers (e.g., CDT -5.56%, PBM -6.15%) moving down togeth...
2 Down

Momentum scanner shows 2 peers (e.g., CDT -5.56%, PBM -6.15%) moving down together, indicating broader biotech pressure around this news.

Historical Context

4 past events · Latest: Jan 07 (Neutral)
Pattern 4 events
Date Event Sentiment Move Catalyst
Jan 07 Industry roundtable Neutral -3.2% CEO to co-lead biopharma manufacturing roundtable at HealthIL Week 2026.
Dec 02 Nine-month results Positive +3.0% Nine-month 2025 results showing higher CDMO revenues and lower R&D expenses.
Oct 06 CDMO grant award Positive +1.9% Israel Innovation Authority grant to expand sterile fill-and-finish capacity.
Sep 02 H1 2025 earnings Positive +0.7% H1 2025 results with CDMO revenue growth and strengthened balance sheet.
Pattern Detected

Recent fundamentally positive updates (CDMO grants and financial progress) tended to see modestly positive or muted price reactions, with no strong divergence pattern.

Recent Company History

Over the last few months, Scinai highlighted CDMO expansion and financial updates. On Sep 2, 2025, H1 2025 results showed CDMO-driven revenue growth and a reduced net loss. A Oct 6, 2025 grant supported fill-and-finish upgrades, followed by nine-month 2025 results on Dec 2, 2025 showing further CDMO momentum. A Jan 7, 2026 roundtable appearance underscored industry positioning. Today’s acquisition and collaboration deepen the same CDMO expansion theme.

Market Pulse Summary

This announcement combines a completed acquisition of Recipharm Israel Ltd. with a long-term commerc...
Analysis

This announcement combines a completed acquisition of Recipharm Israel Ltd. with a long-term commercial collaboration with Recipharm, expanding Scinai’s CDMO reach from early development through commercialization. It builds on prior CDMO-focused grants and financial updates and adds capabilities in APIs and complex modalities. Investors may watch how quickly the Yavne cGMP site is utilized, the flow of referred projects, and revenue contribution from the broader CDMO platform.

Key Terms

cdmo, cgmp, active pharmaceutical ingredients, master quality agreement, +4 more
8 terms
cdmo technical
"a biopharmaceutical company developing inflammation and immunology (I&I) therapeutics and operating a growing CDMO business"
A contract development and manufacturing organization (CDMO) is a company that provides specialized services to help develop and produce pharmaceutical products for other businesses. Think of it as a contract factory that takes a company's recipe and makes the product on their behalf. For investors, CDMOs are important because they support the growth of pharmaceutical companies and can be key partners in bringing new medicines to market.
cgmp technical
"operates a cGMP manufacturing site in Yavne, Israel, providing early chemistry development"
cGMP (current Good Manufacturing Practice) are government-enforced quality standards that manufacturers must follow to ensure drugs, medical devices, and related products are made consistently, safely, and meet specified quality tests. For investors, cGMP compliance is like a restaurant passing health inspections: it reduces the risk of product recalls, regulatory fines, or production stoppages that can hurt revenue and company value, and it supports market access and long-term trust.
active pharmaceutical ingredients medical
"small-scale manufacturing of active pharmaceutical ingredients (APIs) for biopharmaceutical customers"
The active pharmaceutical ingredient (API) is the specific chemical or biological substance in a medicine that produces the intended health effect — the ‘engine’ that treats, prevents or diagnoses a condition. Investors watch APIs because they determine a drug’s cost, quality, regulatory approval and patent protection; shortages, manufacturing problems or competition at the API level can directly affect a drug maker’s sales and valuation.
master quality agreement regulatory
"agreed to establish a Master Quality Agreement and a Tech Transfer Framework Agreement"
A master quality agreement is a standing contract between a product buyer and a manufacturer that sets the agreed standards, tests, responsibilities and remedies for product quality across all batches or projects. Think of it as a shared recipe and inspection checklist that keeps production consistent and compliant with regulations. For investors, it matters because a clear agreement lowers the risk of recalls, delays and extra costs, protecting revenue and reputation tied to product supply and safety.
tech transfer framework agreement technical
"Master Quality Agreement and a Tech Transfer Framework Agreement, creating a pre-defined"
A tech transfer framework agreement is a high-level contract that sets the rules for how one party hands over technology, intellectual property, manufacturing know‑how or processes to another. Think of it as a blueprint that defines who owns what, how the technology will be licensed or paid for, who is responsible for quality and regulatory steps, and the timelines for implementation. Investors care because it shapes potential revenue streams, costs, timing to market and legal or operational risks tied to commercialization.
recombinant proteins medical
"capabilities will now cover recombinant proteins, small molecules, peptides, antibodies and"
Recombinant proteins are proteins produced by inserting the gene that codes for them into a host cell (like bacteria, yeast or cultured animal cells) so the cell becomes a mini factory making that exact protein. Investors care because many medicines, vaccines and diagnostic tests rely on these lab-made proteins; their commercial value depends on how easily they can be produced at scale, protected by patents, and cleared by regulators—similar to how a reliable factory and exclusive recipe affect a consumer product’s profitability.
oligonucleotides medical
"peptides, antibodies and oligonucleotides through a combination of internal capabilities"
Short strands of DNA or RNA designed to bind specific genetic sequences, oligonucleotides act like targeted messages that can turn genes on or off, block harmful proteins, or help detect disease. For investors, they matter because they represent a class of therapeutic and diagnostic products with potential for highly specific treatments, large market value, and distinct development, manufacturing and regulatory risks that can drive big gains or setbacks depending on clinical success and approval.
late-stage clinical medical
"preferred partners for late-stage clinical and commercial manufacturing, subject to capacity"
Late-stage clinical describes the final, large-scale tests of a medical treatment in people that occur after early safety and dosing checks. Think of it as the last full dress rehearsal before regulators decide whether the product can be approved; results carry more weight for safety, effectiveness and commercial potential. For investors, late-stage outcomes strongly influence a drug’s chance of approval, future sales and a company’s valuation.

AI-generated analysis. Not financial advice.

JERUSALEM, Feb. 17, 2026 /PRNewswire/ -- Scinai Immunotherapeutics Ltd. (NASDAQ: SCNI) ("Scinai", or the "Company"), a biopharmaceutical company developing inflammation and immunology (I&I) therapeutics and operating a growing CDMO business, today announced that it has acquired 100% of the shares of Recipharm Israel Ltd., which operates Recipharm's site in Yavne, Israel, and entered into a long-term strategic commercial collaboration with Recipharm.

The transactions significantly expand Scinai's manufacturing footprint, capabilities, and commercial positioning, strengthening its CDMO platform and creating a differentiated, end-to-end development and manufacturing offering spanning early development directly by Scinai and late-stage clinical and commercial supply by Recipharm. Under the collaboration agreement, development activities and tech transfer will be set up between the companies in a manner designed to facilitate an efficient and frictionless graduation of Scinai clients to Recipharm at the appropriate stage. As a result of the acquisition and the collaboration agreement, Scinai's expanded capabilities will now cover recombinant proteins, small molecules, peptides, antibodies and oligonucleotides through a combination of internal capabilities and collaboration with Recipharm.

Acquisition of Recipharm Israel Ltd.

Under the terms of the Share Purchase Agreement, Scinai has acquired Recipharm Israel Ltd., which operates a cGMP manufacturing site in Yavne, Israel, providing early chemistry development and small-scale manufacturing of active pharmaceutical ingredients (APIs) for biopharmaceutical customers' clinical programs. The acquisition was structured as a share purchase to preserve full operational continuity, including employees, quality systems, regulatory approvals, customer contracts, and ongoing operations. The transaction was structured such that Recipharm Israel was transferred with an appropriate working capital position at closing, consistent with maintaining operational continuity.

Following closing, the Yavne site will continue to operate as part of Scinai's CDMO platform, complementing Scinai's existing Jerusalem-based capabilities in early-stage development, analytics, and clinical manufacturing.

The financial terms of the Share Purchase Agreement remain confidential.

Strategic Commercial Collaboration with Recipharm

Concurrently with the acquisition, Scinai and Recipharm entered into a comprehensive Commercial Collaboration Agreement designed to support customer projects across the full development lifecycle.

The collaboration framework provides that:

  • Scinai will serve as a preferred partner for early-stage development and clinical manufacturing projects within the Recipharm ecosystem.
  • Recipharm will serve as one of Scinai's preferred partners for late-stage clinical and commercial manufacturing, subject to capacity and technical suitability.
  • Scinai will have access to Recipharm's global manufacturing network, under predefined commercial terms, providing the ability to support client programs that extend beyond the capabilities of Scinai's internal manufacturing footprint, including the newly acquired Yavne site.
  • The parties will mutually refer client projects and share economics as programs transition from early-stage development at Scinai to late-stage or commercial manufacturing at Recipharm.

As part of the collaboration, the parties have agreed to establish a Master Quality Agreement and a Tech Transfer Framework Agreement, creating a pre-defined contractual basis for quality alignment, regulatory compliance, and efficient transfer of client programs across development stages.

Strategic Rationale and Expected Benefits

The acquisition of Recipharm's manufacturing capabilities in Israel expands Scinai's CDMO footprint in Israel and adds complementary capabilities to its existing Jerusalem site. The Yavne facility broadens Scinai's technical scope and service offering, enabling access to additional customer segments and project types.

Key expected benefits include expanded support for small-molecule programs alongside peptides and liposomes, enhanced handling of complex and hazardous materials, and access to operating infrastructure and equipment that strengthen Scinai's industrial credibility, service breadth, and potential client base.

The Commercial Collaboration Agreement is intended to materially enhance Scinai's competitive positioning in two principal ways. First, it expands the breadth of Scinai's service offerings by enabling the subcontracting of selected capabilities from Recipharm under predefined commercial terms, while allowing Scinai to retain control over project management and optimize service delivery and execution speed by leveraging capacity across its internal operations and, where available, Recipharm's network. Second, it links Scinai's early-stage CDMO offering with Recipharm's global late-stage and commercial manufacturing footprint.

This structure allows Scinai's clients to begin engaging with Recipharm early in development as Scinai's preferred partner for late-stage clinical supply and to benefit from a seamless transition as programs advance. These transitions will be supported by a Master Quality Agreement and a Tech Transfer Framework Agreement to be executed between the parties following closing.

Strategically, this aspect of the collaboration addresses a common industry challenge faced by clients of smaller CDMOs: the risk of friction, delay, and cost overruns when programs transition to a global late-stage or commercial manufacturer. By pre-aligning quality systems, tech-transfer processes, and commercial incentives, the collaboration is designed to streamline these transitions and maintain continuity of service as client programs scale. This positioning differentiates Scinai among smaller CDMOs by offering clients an integrated, end-to-end development pathway from early stage through commercialization.

The collaboration also enables Scinai to participate economically in client programs that successfully progress to later-stage clinical supply or commercial manufacturing at Recipharm's facilities and includes structured referral economics, joint marketing and business development initiatives, and defined name-rights provisions.

Management Commentary

"This transaction fundamentally strengthens Scinai's CDMO platform," said Amir Reichman, Chief Executive Officer of Scinai. "By combining our early-stage development strengths with Recipharm Israel's manufacturing capabilities and Recipharm's global footprint, we are creating a differentiated offering that supports clients from early development through commercialization. Importantly, the collaboration allows Scinai to participate in the long-term success of client programs while maintaining capital discipline and operational focus."

"Ensuring continuity for the Yavne site, its employees and its customers was a key priority for us, and we are pleased to pair that with a strategic collaboration with Scinai," said Greg Behar, Chief Executive Officer of Recipharm. "The agreement creates a clear pathway for programs to progress efficiently into Recipharm's global development and commercial manufacturing network."

About Recipharm Israel Ltd.

Recipharm Israel Ltd. operates a cGMP development and manufacturing facility in Yavne, Israel, dedicated to early chemistry development and small-scale manufacturing of active pharmaceutical ingredients (APIs) for clinical programs. The site supports projects from first synthesis through Phase I and Phase II clinical supply and serves biopharmaceutical customers across multiple geographies.

The Yavne facility comprises approximately 900 square meters of built area and includes multiple production rooms, analytical laboratories, an R&D laboratory, and controlled cleanroom environments. The site provides integrated capabilities spanning medicinal chemistry, route scouting and optimization, scale-up development, analytical method development and validation, stability studies, and small-batch cGMP manufacturing for toxicology and clinical studies.

About Recipharm

Recipharm is a leading Contract Development and Manufacturing Organisation (CDMO) employing over 5,000 employees worldwide. Recipharm provides expertise in development and manufacturing across oral dosage, sterile fill & finish and advanced biologics; clinical trial material development and manufacturing services; and pharmaceutical product development. Its Advanced Bio segment works with customers to develop and commercialise advanced therapy medicinal products (ATMPs): pre-clinical to clinical development, commercial development and manufacture for new biological modalities, encompassing technologies based on live viruses and viral vectors, live-microbial biopharmaceutical products, nucleic acid-based mRNA and plasmid DNA production.

Recipharm manufactures several hundred different products to customers ranging from big pharma to smaller research and development companies. It operates development and manufacturing facilities in France, Germany, India, Italy, Portugal, Spain, Sweden and the US.

For more information on Recipharm, please visit www.recipharm.com and www.recipharm-ab.com 

About Scinai Immunotherapeutics

Scinai Immunotherapeutics Ltd. (NASDAQ: SCNI) is a biopharmaceutical company with two complementary business units:

  • Scinai Bioservices, a boutique CDMO providing analytical method development, process development, and clinical cGMP manufacturing services for biotech clients worldwide.
  • Scinai R&D, focused on developing innovative inflammation and immunology therapeutics based on NanoAbs (VHH antibody fragments) with unique physicochemical properties suitable for advanced mono- and multi-specific antibody formats.

 Company website: www.scinai.com 

Company Contacts

Investor Relations - Allele Capital Partners | +1 978 857 5075 | aeriksen@allelecapital.com 
Business Development | +972 8 930 2529 | bd@scinai.com

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Litigation Reform Act of 1995. Words such as "expect," "believe," "intend," "plan," "continue," "may," "will," "anticipate," and similar expressions are intended to identify forward-looking statements. All statements, other than statements of historical facts, are forward-looking statements, including statements regarding the expected benefits of the agreements with Recipharm described in this press release. These forward-looking statements reflect management's current views with respect to certain current and future events and are subject to various risks, uncertainties and assumptions that could cause the results to differ materially from those expected by the management of Scinai Immunotherapeutics Ltd. Risks and uncertainties include, but are not limited to; the risk that the currently expected benefits from the Share Purchase Agreement and Commercial Collaboration Agreement will not be as expected, including that Scinai will not be successful in expanding support for small-molecule programs alongside peptides and liposomes, strengthening Scinai's industrial credibility, service breadth, and potential client base, or materially enhancing Scinai's competitive positioning; that the Company will be unable to remain compliant with the continued listing requirements of Nasdaq; lower than anticipated revenues of Scinai's CDMO business in 2025 and thereafter, failure to sign agreements with other potential clients of the CDMO business; failure to receive grants under the EU STEP program or a delay in receiving grant decisions; delay in commencement of commercial operation of advanced sterile fill-and-finish system; a delay in the commencement and results of pre-clinical and clinical studies, the risk of delay in, Scinai's inability to conduct, or the unsuccessful results of, its research and development activities, including the contemplated in-vivo studies and a clinical trial; the risk that Scinai will not be successful in expanding its CDMO business or in-license other NanoAbs; the risk that Scinai may not be able to secure additional capital on attractive terms, if at all; the risk that the therapeutic and commercial potential of NanoAbs will not be met or that Scinai will not be successful in bringing the NanoAbs towards commercialization; the risk of a delay in the preclinical and clinical trials data for NanoAbs, if any; the risk that our business strategy may not be successful; Scinai's ability to acquire rights to additional product opportunities; Scinai's ability to enter into collaborations on terms acceptable to Scinai or at all; timing of receipt of regulatory approval of Scinai's manufacturing facility in Jerusalem, if at all or when required; the risk that the manufacturing facility will not be able to be used for a wide variety of applications and other vaccine and treatment technologies; and the risk that drug development involves a lengthy and expensive process with uncertain outcomes. More detailed information about the risks and uncertainties affecting the Company is contained under the heading "Risk Factors" in the Company's Annual Report on Form 20-F filed with the Securities and Exchange Commission ("SEC") on May 7, 2025, and the Company's subsequent filings with the SEC. Scinai undertakes no obligation to revise or update any forward-looking statement for any reason.

Photo: https://mma.prnewswire.com/media/2905104/Scinai_Recipharm.jpg

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/scinai-announces-completion-of-acquisition-of-recipharm-israel-ltd-and-strategic-commercial-collaboration-with-recipharm-302689449.html

SOURCE Scinai Immunotherapeutics Ltd.

FAQ

What did Scinai announce about the Recipharm Israel Ltd. acquisition on February 17, 2026?

Scinai completed the acquisition of 100% of Recipharm Israel Ltd.'s Yavne cGMP site. According to the company, the purchase adds early chemistry development and small-scale API manufacturing to Scinai's CDMO platform, preserving employees, regulatory approvals, and customer contracts.

How does the Scinai–Recipharm commercial collaboration affect SCNI's CDMO services?

The collaboration links Scinai's early-stage development with Recipharm's late-stage and commercial manufacturing. According to the company, predefined referral economics, Master Quality and Tech Transfer agreements aim to streamline transitions and widen service offerings globally.

Will Scinai retain operational continuity at the acquired Yavne site after closing?

Yes — Scinai structured the share purchase to preserve full operational continuity at Yavne. According to the company, employees, quality systems, regulatory approvals, customer contracts and ongoing operations were transferred to maintain continuity.

What limitations apply to Scinai using Recipharm for late-stage manufacturing under the February 17, 2026 agreement?

Late-stage and commercial manufacturing via Recipharm is subject to capacity and technical suitability. According to the company, Recipharm will serve as a preferred partner when capacity and technical fit permit, not unconditionally.

Did Scinai disclose the financial terms of the Recipharm Israel acquisition in the February 17, 2026 announcement?

No — the financial terms of the share purchase agreement remain confidential. According to the company, the specific purchase price and related financial terms were not disclosed in the announcement.

How will the Master Quality Agreement and Tech Transfer Framework benefit SCNI clients after the acquisition?

They create predefined quality alignment and tech-transfer processes to reduce friction during program transitions. According to the company, these agreements are designed to facilitate efficient graduation of clients from early-stage work at Scinai to late-stage supply at Recipharm.
Scinai Immunotherapeutics Ltd.

NASDAQ:SCNI

SCNI Rankings

SCNI Latest News

SCNI Latest SEC Filings

SCNI Stock Data

2.58M
776.74k
Biotechnology
Biological Products, (no Diagnostic Substances)
Link
Israel
JERUSALEM