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Financial Snapshot

Revenue
Last 4 Quarters
N/A
Gross Margin
Last 4 Quarters
N/A
Net Income
TTM
-$7.136M
Current Assets
2026 Q1
Current Liabilities
2026 Q1
Current Ratio
2026 Q1
1.56%
Total Assets
2026 Q1
Total Liabilities
2026 Q1
Book Value
2026 Q1
-11.01M
Cash
2026 Q1
P/E
Last 4 Quarters
N/A
Free Cash Flow
Last 4 Quarters
N/A

Stock Price

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Market Cap: $8.7366 Million

About Brainstorm Cell Therapeutics Inc

Brainstorm Cell Therapeutics Inc. (OTCQB: BCLI) is a clinical-stage biotechnology company developing autologous cellular therapies for neurodegenerative diseases. The company has no approved products and generates no product revenue, operating entirely on external funding while advancing its NurOwn cell therapy platform through clinical development. NurOwn is designed to treat amyotrophic lateral sclerosis (ALS), progressive multiple sclerosis, Alzheimer's disease, and other neurodegenerative conditions. The platform uses mesenchymal stem cells engineered to secrete neurotrophic factors (MSC-NTF cells), and the company has also conducted preclinical research into NurOwn-derived exosomes for conditions including acute respiratory distress syndrome. As of the 10-K filed March 31, 2026 (fiscal year ended 2025), the company remained pre-commercial, with operations spanning the United States and Israel. Brainstorm faces active securities litigation related to its NurOwn clinical trial disclosures and FDA interactions, with several claims surviving a motion to dismiss as of September 15, 2025.

Revenue model
Brainstorm Cell Therapeutics has no disclosed product revenue. The company is pre-commercial and funds operations through capital raises. No licensing, royalty, or partnership revenue streams are described in the filing excerpts.
Products and services
NurOwn (MSC-NTF cell therapy platform): autologous mesenchymal stem cells engineered to secrete neurotrophic factors, in clinical development for ALS, progressive multiple sclerosis, and Alzheimer's disease. NurOwn-derived exosomes (small extracellular vesicles): preclinical stage, evaluated in mouse models of ARDS as of a study published January 20, 2021.
Customers and end markets
No commercial customers as of the filing date. Target end markets are patients with neurodegenerative diseases, specifically ALS, progressive multiple sclerosis, and Alzheimer's disease. Reimbursement would ultimately flow through Medicare, Medicaid, and private insurers upon any future approval.
Value-chain role
Clinical-stage drug developer. Brainstorm conducts cell therapy research, manages clinical trials, and handles regulatory interactions with the FDA. Manufacturing of autologous cell therapies is part of the development process. The company operates under U.S. and Israeli regulatory frameworks and is subject to HIPAA, CCPA, and Israeli data protection law.
Geographic exposure
Operations in the United States and Israel, as indicated by references to Israeli data protection law obligations and U.S. federal and state regulatory compliance described in the fiscal year 2025 10-K.

Source: SEC 10-K, filed 2026-03-31

Industry: Biological Products, (No Diagnostic Substances) Peers: Savara Inc Anixa Biosciences Inc CEL-SCI Corp CHIMERIX INC Clovis Oncology, Inc. Larimar Therapeutics Inc Viracta Therapeutics, Inc. Vor Biopharma Inc

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