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Scinai Immunotherapeutics (NASDAQ: SCNI) acquires Recipharm Israel and deepens CDMO collaboration

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Rhea-AI Filing Summary

Scinai Immunotherapeutics Ltd. completed the acquisition of 100% of the shares of Recipharm Israel Ltd., which operates a cGMP active pharmaceutical ingredient manufacturing site in Yavne, Israel, and entered into a long-term strategic commercial collaboration with Recipharm.

The deal adds a second Israeli facility to Scinai’s CDMO platform, broadening its services from early chemistry development and small-scale API manufacturing through to late-stage clinical and commercial supply via Recipharm’s global network. The collaboration is structured around planned Master Quality and Tech Transfer Framework Agreements to support seamless client transitions as programs advance.

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Insights

Scinai adds an API site and a global CDMO partner to deepen its development-to-commercial offering.

Scinai has acquired Recipharm Israel Ltd., a cGMP site in Yavne providing early chemistry development and small-scale API manufacturing for clinical programs. The facility is transferred with employees, quality systems, regulatory approvals and customer contracts to preserve operational continuity within Scinai’s CDMO platform.

Concurrently, Scinai signed a Commercial Collaboration Agreement with Recipharm, aiming to link Scinai’s early-stage services to Recipharm’s global late-stage and commercial manufacturing footprint. Pre-agreed Master Quality and Tech Transfer Framework Agreements are intended to reduce friction, delays and cost overruns when client programs scale.

The structure allows Scinai to retain project management while subcontracting selected capabilities from Recipharm and participating economically when client programs reach later-stage or commercial manufacturing at Recipharm facilities. Actual impact will depend on execution, client uptake and the broader risk factors described, including revenue growth in the CDMO business and access to capital.

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 6-K

 

Report of Foreign Private Issuer Pursuant to Rule 13a-16 or 15d-16

Under the Securities Exchange Act of 1934

 

For the Month of February 2026

 

Commission File Number: 001-37353

 

SCINAI IMMUNOTHERAPEUTICS LTD.

(Translation of registrant’s name into English)

 

Jerusalem BioPark, 2nd Floor

Hadassah Ein Kerem Campus

Jerusalem, Israel

(Address of principal executive office)

 

Indicate by check mark whether the registrant files or will file annual reports under cover Form 20-F or Form 40-F.

 

Form 20-F ☒       Form 40-F ☐

 

 

 

 

 

Explanatory Note 

 

On February 17, 2026, Scinai Immunotherapeutics Ltd. issued a press release announcing completion of acquisition of Recipharm Israel Ltd. and strategic commercial collaboration with Recipharm.

 

A copy of the press release is furnished herewith as Exhibit 99.1.

 

This Report on Form 6-K (other than the paragraphs under “Management Commentary”) is hereby incorporated by reference into the registrant’s Registration Statements on Form S-8 (File No. 333-291460333-271293 and File No. 333-239344) and Form F-3 (File No. 333-274078 and File No. 333-276767), to be a part thereof from the date on which this report is submitted, to the extent not superseded by documents or reports subsequently filed or furnished.

 

Exhibit Index

 

Exhibit No.   Description
99.1   Press release dated February 17, 2026.

 

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SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

  Scinai Immunotherapeutics Ltd.
     
Date: February 17, 2026 By: /s/ Amir Reichman
    Amir Reichman
    Chief Executive Officer

 

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Exhibit 99.1

 

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

 

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.

 

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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

 

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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

 

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FAQ

What transaction did Scinai Immunotherapeutics (SCNI) complete with Recipharm Israel Ltd.?

Scinai completed the acquisition of 100% of the shares of Recipharm Israel Ltd., which operates a cGMP facility in Yavne, Israel. The site provides early chemistry development and small-scale API manufacturing for clinical programs, and will now operate as part of Scinai’s CDMO platform.

How does the Recipharm collaboration change Scinai Immunotherapeutics (SCNI)’s CDMO offering?

The collaboration links Scinai’s early-stage CDMO services with Recipharm’s global late-stage and commercial manufacturing network. It allows Scinai to subcontract selected capabilities, retain project management, and support client programs from early development through commercialization under predefined quality and tech-transfer frameworks.

What capabilities does the newly acquired Yavne site add for Scinai Immunotherapeutics (SCNI)?

The Yavne facility adds cGMP early chemistry development and small-scale API manufacturing for clinical programs. It broadens Scinai’s technical scope, enabling expanded support for small-molecule programs alongside peptides and liposomes, enhanced handling of complex and hazardous materials, and access to additional infrastructure and equipment in Israel.

What are the expected strategic benefits of Scinai Immunotherapeutics (SCNI)’s agreement with Recipharm?

The agreement is intended to enhance Scinai’s competitive positioning by expanding service breadth via Recipharm’s capabilities and creating an end-to-end development pathway. It targets reduced friction, delays and cost overruns during tech transfers, and includes referral economics, joint marketing, business development initiatives and defined name-rights provisions.

How will quality and tech transfer be managed between Scinai Immunotherapeutics (SCNI) and Recipharm?

Scinai and Recipharm plan to establish a Master Quality Agreement and a Tech Transfer Framework Agreement. These are intended to pre-align quality systems, regulatory compliance, and tech-transfer processes, supporting efficient and consistent transitions of client programs across development stages between the two organizations.

What risks does Scinai Immunotherapeutics (SCNI) highlight regarding the Recipharm agreements and CDMO strategy?

Scinai notes risks that expected benefits from the Share Purchase and Commercial Collaboration Agreements may not materialize, including challenges in expanding small-molecule support, strengthening credibility and client base, or enhancing positioning. Additional risks include Nasdaq listing compliance, CDMO revenue levels, capital access, regulatory approvals and NanoAb development outcomes.

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