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SCNI

Scinai Immunotherapeutics Ltd.

Biopharma developer (SEC filing verified)·Jerusalem, Israel·CEO: Mr. Amir Reichman M.B.A., M.Sc.

SCNI evidence brief

What we can confirm

Market Cap:
$1.7M

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $1.7M
BioSniper AIPage evidence connected

Prepared research question

What matters most for SCNI—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · SCNI

Scinai Immunotherapeutics Ltd. is a biopharmaceutical company with a dual business model combining in-house R&D in inflammation and immunology (including NanoAbs and the PC111 program) with a contract development and manufacturing (CDMO) platform, aiming to manage development risk and capital constraints [sec · filed 2026-04-01].

Key risk: No commercialized products

Market Cap

$1.7M

Cash Runway

—

Lead Asset

—

Next Catalyst

—

Financial data as of Dec 31, 2025.

AI OverviewAI overview is shown in English only.

Scinai Immunotherapeutics Ltd. is a biopharmaceutical company with a dual business model combining in-house R&D in inflammation and immunology (including NanoAbs and the PC111 program) with a contract development and manufacturing (CDMO) platform, aiming to manage development risk and capital constraints [sec · filed 2026-04-01].

  • Dual business model: Scinai operates both a drug development unit (Scinai R&D) and a CDMO platform (Scinai Biopharma Services Ltd.) to generate revenue and support pipeline development [sec · filed 2026-04-01].
  • Cash & equivalents of $1.7M and shareholders' equity of $8.1M as of 2025-12-31 [sec].
  • Pipeline includes NanoAbs (VHH antibody fragments) from MPG/UMG collaboration targeting clinically validated pathways, and the PC111 program (fully human monoclonal antibody) with EMA orphan drug designation for pemphigus [sec · filed 2026-04-01].
  • CDMO platform supports recombinant proteins, antibodies, peptides, small molecules, and oligonucleotides, with integration into Recipharm's network for lifecycle support [sec · filed 2026-04-01].
  • The company has not yet commercialized any product candidate and may never become profitable [sec · filed 2026-04-01].

What works

  • Dual business model combining R&D and CDMO operations provides operational expertise in CMC, generates external revenues, and supports internal pipeline development [sec · filed 2026-04-01].
  • Access to externally sourced assets with defined biological rationale and potential regulatory advantages, such as PC111 with EMA orphan drug designation, may offer expedited regulatory pathways [sec · filed 2026-04-01].
  • Focus on clinically validated targets for NanoAb programs may reduce scientific risk and support more efficient development [sec · filed 2026-04-01].
  • Integration with Recipharm allows client programs to transition from early-stage to commercial manufacturing, enabling participation in downstream economics [sec · filed 2026-04-01].

What to weigh

  • The company has not yet commercialized any product candidate and may never become profitable [sec · filed 2026-04-01].
  • The IL-17 program is under strategic review; there is no assurance that the program will continue under its current structure, timeline, or at all, which could result in loss of rights under the license agreement [sec · filed 2026-04-01].
  • Cash & equivalents of $1.7M as of 2025-12-31 is relatively low for a biotech with multiple R&D programs and no commercial revenue [sec].
  • The company's CDMO business faces uncertainty in scaling commercial activity and client acquisition, with no assurance of sustained growth [sec · filed 2026-04-01].

From the filings

Quoted directly from source documents.

  • Dual business model combining R&D and CDMO operations

    “We are a biopharmaceutical company with two complementary business units: (i) Scinai R&D, focused on the development of innovative therapeutics in inflammation and immunology, and (ii) our contract development and manufacturing organization (CDMO) business, which operates through”

    SEC filings · April 1, 2026

  • PC111 has orphan drug designation from EMA for pemphigus

    “PC111, which has received orphan drug designation for pemphigus from the European Medicines Agency”

    SEC filings · April 1, 2026

  • No product candidate has been commercialized

    “We have not yet commercialized any product candidate(s), and we may never become profitable.”

    SEC filings · April 1, 2026

Risks & what to watch (4)›

Key risks

  • No commercialized products — The company has not yet commercialized any product candidate and may never become profitable [sec · filed 2026-04-01].
  • IL-17 program uncertainty — The IL-17 program is under strategic review; discontinuation could result in loss of license rights and materially affect business [sec · filed 2026-04-01].
  • Low cash reserves — Cash & equivalents of $1.7M as of 2025-12-31 is limited for a biotech with multiple R&D programs and no commercial revenue [sec].
  • CDMO growth uncertainty — No assurance of sustained growth in CDMO business through client acquisition or repeat engagements [sec · filed 2026-04-01].

What to watch

  • Strategic decision on the IL-17 program: any modification, delay, or discontinuation could affect license rights and business prospects [sec · filed 2026-04-01].
  • Progress of the PC111 program, including potential clinical milestones and regulatory interactions given its orphan drug designation [sec · filed 2026-04-01].
  • CDMO business development: ability to scale commercial activity and acquire new clients [sec · filed 2026-04-01].
  • Cash runway and potential need for additional financing given $1.7M cash as of 2025-12-31 [sec].

Sources: SEC filings · Generated September 25, 2026 · How we verify sources →

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Evidence & data

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

4

Total value held

$15K

HolderSharesValue
xtx topco ltd24,041$13K
rhumbline advisers1,878$1K
ubs group ag919$524
morgan stanley58$33

Short Interest

as of May 1, 2026
% of float
2.1%
Days to cover
1.4
Shares short
72,973
Daily short volume (Aug 13, 2026)
50.7%

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

SCNI short interest

Frequently asked questions

What is the AI investment thesis for Scinai Immunotherapeutics Ltd.?

Scinai Immunotherapeutics Ltd. is a biopharmaceutical company with a dual business model combining in-house R&D in inflammation and immunology (including NanoAbs and the PC111 program) with a contract development and manufacturing (CDMO) platform, aiming to manage development risk and capital constraints [sec · filed 2026-04-01].

Who is the CEO of Scinai Immunotherapeutics Ltd.?

Mr. Amir Reichman M.B.A., M.Sc. is the chief executive officer of Scinai Immunotherapeutics Ltd. (SCNI).

Where is Scinai Immunotherapeutics Ltd. headquartered?

Scinai Immunotherapeutics Ltd. (SCNI) is headquartered in Jerusalem, Israel.

923 companies304,844 SEC filings22,644 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.