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. 333-291460, 333-271293 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to be a part thereof from the date on which this report is submitted, to the extent not superseded by documents or reports subsequently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 March 2, 2026. |
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
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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