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Financial Snapshot

Revenue
TTM
$3.936M
Gross Margin
Last 4 Quarters
N/A
Net Income
TTM
-$86.02M
Current Assets
2026 Q1
Current Liabilities
2026 Q1
Current Ratio
2026 Q1
614.76%
Total Assets
2026 Q1
Total Liabilities
2026 Q1
Book Value
2026 Q1
$30.90M
Cash
2026 Q1
P/E
Last 4 Quarters
N/A
Free Cash Flow
TTM
-$27.20M

Stock Price

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Market Cap: $216.53 Million

About CAMP4 Therapeutics Corp

CAMP4 Therapeutics Corp (CAMP) is a clinical-stage biopharmaceutical company focused on discovering and developing RNA-targeting therapeutics designed to upregulate gene expression and restore healthy protein levels in genetic diseases. Revenue comes from collaboration and license agreements, totaling $3.5 million in FY2025 and $0.7 million in FY2024. No product sales revenue has been generated as of the 10-K filed March 5, 2026. The lead program, CMP-002, is an intrathecally delivered antisense oligonucleotide targeting SYNGAP1-related disorder, a severe developmental and epileptic encephalopathy affecting an estimated 21,000 individuals in the United States and five largest European markets, for which no approved disease-modifying therapies exist. The company's RAP Platform underlies its pipeline and proprietary IP estate. Josh Mandel-Brehm serves as President and Chief Executive Officer.

Revenue model
Collaboration and license agreement revenue: $3.5 million in FY2025, $0.7 million in FY2024. No product sales revenue generated. Future revenue, if any, would come from product sales upon regulatory approval or payments from collaboration and license agreements.
Products and services
CMP-002: intrathecally delivered antisense oligonucleotide (ASO) targeting the SYNGAP1 gene to increase gene expression and restore SYNGAP protein levels, in development for SYNGAP1-related disorder. RAP Platform: proprietary RNA-targeting technology platform for upregulating gene expression.
Customers and end markets
End market: patients with rare genetic diseases, specifically SYNGAP1-related disorder (developmental and epileptic encephalopathy). Estimated patient population of approximately 21,000 in the United States and five largest European markets. Collaborators and licensors are counterparties to revenue-generating agreements.
Value-chain role
Drug discovery and clinical-stage development. Relies on contract research organizations (CROs) and contract manufacturing organizations (CMOs) for clinical trials and preclinical studies. Licenses foundational technology from the Whitehead Institute, with aggregate license maintenance and patent fees of approximately $0.9 million paid through December 31, 2025 under that agreement.
Geographic exposure
Headquartered in the United States. Target patient population identified in the United States and five largest European markets. No product commercialization geographic exposure disclosed in the filing excerpts.

Source: SEC 10-K, filed 2026-03-05

Industry: Pharmaceutical Preparations

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