Caribou Biosciences, Inc.
NASDAQ Global SelectCapital Structure
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in mil. unless spec.Working Capital
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in mil. unless spec.Growth Rates
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in mil. unless spec.Quarterly Revenue
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in mil. unless spec.Quarterly Earnings Per Share
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in mil. unless spec.Quarterly Dividends Per Share
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in mil. unless spec.- CEO
- Rachel E. Haurwitz
- Full Time Employees
- 97
- Sector
- Healthcare
- Industry
- Biotechnology
- Address
- 2929 7th Street Berkeley CA United States of America 94710
- IPO Date
- Jul 23, 2021
- CIK
- 0001619856
- Website
- cariboubio.com
- Similar Companies
- Business
- Caribou Biosciences, Inc. (NASDAQ: CRBU) is a clinical-stage biopharmaceutical company leveraging proprietary CRISPR-based genome-editing technologies to develop allogeneic, off-the-shelf CAR-T cell therapies for hematologic malignancies and autoimmune diseases. Founded in 2011 and headquartered in Berkeley, California, the company employs its patented Cas9 and Cas12a chRDNA platforms for precise multiplex editing, including TRAC knockout and CAR insertion, PD-1 knockout for checkpoint disruption, and B2M-HLA-E fusion for immune cloaking; its lead product candidate, vispa-cel (formerly CB-010), is an anti-CD19 CAR-T therapy in the ANTLER Phase 1 trial for relapsed or refractory B cell non-Hodgkin lymphoma (r/r B-NHL), featuring FDA Regenerative Medicine Advanced Therapy, Fast Track, and Orphan Drug designations, while CB-011 is an anti-BCMA CAR-T therapy in the CaMMouflage Phase 1 trial for relapsed or refractory multiple myeloma (r/r MM) with Fast Track and Orphan Drug status. Caribou operates primarily in the United States with international ambitions through scalable manufacturing for broad patient access to rapid, off-the-shelf treatments targeting oncology and autoimmune indications. In April 2025, the company announced a strategic pipeline prioritization, discontinuing earlier-stage programs like CB-012 and CB-020, reducing its workforce by 32%, and implementing cost cuts to extend its cash runway into the second half of 2027, while maintaining focus on CB-010 and CB-011; recent milestones include positive Phase 1 data disclosures in November 2025 for both programs, with vispa-cel demonstrating efficacy in second-line large B cell lymphoma and CB-011 establishing a 450 million CAR-T cell recommended dose for expansion in r/r MM, alongside ongoing FDA discussions for potential pivotal trials.
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