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€12m FENG bid backs Scinai (NASDAQ: SCNI) PC111 and PinCell option

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(Neutral)
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Form Type
6-K

Rhea-AI Filing Summary

Scinai Immunotherapeutics has signed a Second Amendment to its Binding Option Agreement to acquire PinCell and aligned the option timelines with a European grant process. The deadline to meet option conditions is now August 31, 2026, with an exercise period through September 30, 2026.

Scinai also submitted a revised application to the FENG SMART Path program seeking €12 million in non-dilutive, non‑repayable funding to co-finance a €15 million R&D program for PC111, targeting severe autoimmune skin diseases. A funding decision is expected in about three to four months and, if awarded, could support early clinical development and human proof of concept while limiting shareholder dilution.

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Insights

Scinai ties a potential €12m non-dilutive grant to its option to acquire PinCell and advance PC111.

Scinai Immunotherapeutics is pursuing a FENG SMART Path grant of €12 million to fund a €15 million program for PC111, a monoclonal antibody for pemphigus vulgaris and SJS/TEN. The application targets about 80% project co‑financing, which would substantially offset development costs if approved.

The Second Amendment extends option milestones to August 31, 2026 for condition fulfillment and September 30, 2026 for exercise, aligning the acquisition timeline for PinCell with the grant review process. Management frames this as enhancing competitiveness and preserving balance sheet flexibility.

Actual impact depends on grant approval, timing of disbursements, and clinical progress. Risks highlighted include the possibility of reduced or rejected funding, failure to exercise the option, development setbacks for PC111, regulatory uncertainties around accelerated pathways, and broader capital and Nasdaq listing risks identified in prior SEC filings.

 

 

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 March 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 March 2, 2026, Scinai Immunotherapeutics Ltd. issued a press release announcing the execution of second amendment to its Binding Option Agreement for the acquisition of PinCell S.r.l and submission of revised application under the European Funds for the Modern Economy (FENG) SMART Path program.

 

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

 

This Report on Form 6-K 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.

 

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Exhibit Index

 

Exhibit No.   Description
99.1   Press release dated March 2, 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: March 23, 2026 By: /s/ Amir Reichman
    Amir Reichman
    Chief Executive Officer

 

 

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Exhibit 99.1

 

Scinai Signs Second Amendment to PinCell Option Agreement and Submits Revised €12 Million Non-Dilutive FENG Application to Advance PC111 Through Human Proof of Concept

 

JERUSALEM, March 2, 2026 /PRNewswire/ -- Scinai Immunotherapeutics Ltd. (Nasdaq: SCNI);(“Scinai” or the “Company”), today announced the execution of a Second Amendment to its Binding Option Agreement for the acquisition of PinCell S.r.l., and the submission of a revised application under the European Funds for the Modern Economy (FENG) SMART Path program.

 

The Company’s revised application seeks €12 million in non-dilutive, non-repayable funding to support a €15 million integrated R&D program for PC111 a fully human monoclonal antibody targeting soluble Fas Ligand (sFasL) for the treatment of pemphigus vulgaris (PV) and Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis (SJS/TEN), representing 80% project co-financing. The Company expects a funding decision within approximately three to four months following submission.

 

The Second Amendment aligns the option timeline with the grant evaluation process. Under the amended terms, the deadline for fulfillment of the option conditions extends to August 31, 2026, and the option exercise period extends to September 30, 2026.

 

 

 

 

 

Strengthened and Repositioned Application

 

The Company has submitted a revised application under the SMART Path program reflecting structural enhancements to project design and translational scope. The updated submission advances PC111 through a milestone-driven framework culminating in integrated non-clinical and First-in-Human datasets intended to support data-driven progression decisions. Management believes the revised structure enhances the project’s competitiveness under program criteria.

 

Strategic Financing Catalyst

 

If awarded, the €12 million grant would enable Scinai to advance PC111 through completion of early clinical development and human proof of concept while preserving balance sheet flexibility and minimizing shareholder dilution.

 

PC111 is a first-in-class therapeutic candidate for severe autoimmune blistering diseases, including pemphigus vulgaris (PV) and Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis (SJS/TEN). There are currently no approved therapies for SJS/TEN.

 

Subject to clinical results and regulatory engagement, management believes PC111 may qualify for accelerated regulatory pathways in severe orphan dermatologic indications given the high unmet medical need.

 

“The revised submission reflects a structurally strengthened innovation framework and a clearly defined translational pathway through human proof of concept,” said Amir Reichman, Chief Executive Officer of Scinai. “Securing substantial non-dilutive funding at this stage would meaningfully de-risk the PC111 program while maintaining disciplined capital allocation and preserving strategic flexibility.”

 

About Scinai Immunotherapeutics

 

Scinai Immunotherapeutics Ltd. (NASDAQ: SCNI) is a biopharmaceutical company operating a contract development and manufacturing organization (CDMO) alongside a focused immunology R&D pipeline.

 

The Company’s wholly owned CDMO unit provides fee-for-service development and manufacturing solutions to biotech and pharmaceutical companies across early-stage biologics and small-molecule programs. In parallel, Scinai is advancing a focused immunology pipeline, including PC111 and next-generation NanoAb-based programs, and is pursuing strategic partnerships, co-development agreements and regional licensing opportunities.

 

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 U.S. Private Securities Litigation Reform Act of 1995 and other applicable securities laws. Forward-looking statements include, among other things, statements regarding the planned submission and anticipated review timeline of the revised FENG grant application; the potential award, amount and non-dilutive nature of funding under the European Funds for the Modern Economy (FENG) SMART Path program; the Company’s ability to satisfy the conditions for and exercise its option to acquire PinCell S.r.l.; the expected scope, timing and outcomes of the PC111 development program, including completion of early clinical studies and generation of translational evidence; the potential eligibility of PC111 for accelerated regulatory pathways; and the Company’s strategic and capital allocation plans. Words such as “expects,” “intends,” “plans,” “believes,” “may,” “will,” “anticipates,” “estimates,” “targets,” and similar expressions are intended to identify forward-looking statements.

 

These statements are based on current expectations and assumptions and are subject to a number of risks, uncertainties and other factors that could cause actual results to differ materially from those expressed or implied by such forward-looking statements. These risks and uncertainties include, without limitation: the risk that the FENG grant application is not approved, is approved in a lower amount than anticipated, or is subject to conditions that delay, limit or prevent access to funding; delays in grant review or disbursement timelines; the Company’s ability to secure alternative financing required under the option agreement if grant funding is not obtained; the risk that the Company does not satisfy the conditions for, or otherwise does not, exercise the option to acquire PinCell; risks inherent in preclinical and clinical development, including delays in or unsuccessful results from studies of PC111; regulatory risks, including the risk that accelerated or other expedited pathways may not be available; risks relating to intellectual property protection; the Company’s ability to maintain compliance with Nasdaq continued listing requirements; risks associated with the Company’s need for additional capital; and general market and economic conditions.

 

More detailed information regarding these and other risks and uncertainties is included under the heading “Risk Factors” in the Company’s Annual Report on Form 20-F filed with the U.S. Securities and Exchange Commission on May 7, 2025, and in the Company’s subsequent filings with the SEC.

 

Forward-looking statements speak only as of the date of this press release. Except as required by applicable law, the Company undertakes no obligation to update or revise any forward-looking statements to reflect new information, future events, or otherwise.

 

 

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FAQ

What did Scinai Immunotherapeutics (SCNI) announce in this Form 6-K?

Scinai reported two related strategic steps. It executed a Second Amendment to its Binding Option Agreement to acquire PinCell and submitted a revised application to the FENG SMART Path program, seeking significant non-dilutive funding to advance its PC111 autoimmune dermatology program through early clinical development.

How much FENG SMART Path funding is Scinai (SCNI) seeking and for what purpose?

Scinai’s revised FENG application seeks €12 million. The funding would co-finance a €15 million integrated R&D program for PC111, supporting non-clinical work and First‑in‑Human studies aimed at generating human proof-of-concept data in severe autoimmune blistering skin diseases.

What is PC111 and which diseases is Scinai targeting with it?

PC111 is a fully human monoclonal antibody targeting soluble Fas Ligand. Scinai is developing it for pemphigus vulgaris and Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis (SJS/TEN), severe autoimmune blistering diseases where, according to the company, no approved therapies currently exist for SJS/TEN.

When does Scinai expect a decision on the revised FENG grant application?

The company anticipates a relatively near-term review outcome. Scinai states it expects a funding decision from the FENG SMART Path program approximately three to four months after submission, potentially influencing how it finances PC111’s early clinical development and options regarding the PinCell acquisition.

How were the option deadlines to acquire PinCell changed in the amendment?

The amendment extends and aligns key option milestones. Under the revised terms, the deadline to fulfill conditions for exercising the option now runs to August 31, 2026, and the actual option exercise period extends to September 30, 2026, matching the expected timeline of the FENG grant evaluation.

Why does Scinai view the potential €12 million FENG grant as strategically important?

The grant would provide non-dilutive, non‑repayable capital. Management indicates that, if awarded, it could fund PC111 through early clinical development and human proof of concept while preserving balance sheet flexibility and limiting shareholder dilution, although approval and terms remain uncertain.

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Scinai Immunotherapeutics Ltd.

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Biotechnology
Biological Products, (no Diagnostic Substances)
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Israel
JERUSALEM