Filing Analysis
Caribou Biosciences announced its financial results for the first quarter ended March 31, 2026, and provided a general business update. The disclosure was made via a press release furnished as an exhibit to the filing.
Key Facts
- Announced financial results for the quarter ended March 31, 2026
- Provided a business update in the accompanying press release (Exhibit 99.1)
- The report was filed under Item 2.02 (Results of Operations and Financial Condition)
- The filing was signed by President and CEO Rachel E. Haurwitz, Ph.D.
Caribou Biosciences announced that the FDA has granted Regenerative Medicine Advanced Therapy (RMAT) designation to CB-011, its allogeneic anti-BCMA CAR-T cell therapy for relapsed or refractory multiple myeloma. The candidate is currently being evaluated in the ongoing CaMMouflage Phase 1 clinical trial.
Key Facts
- FDA granted RMAT designation for CB-011 on March 31, 2026.
- CB-011 is an allogeneic anti-BCMA CAR-T cell therapy product candidate.
- The designation is for the treatment of relapsed or refractory multiple myeloma (r/r MM).
- CB-011 is currently in the CaMMouflage Phase 1 clinical trial.
Caribou Biosciences announced its financial results for the fourth quarter and fiscal year ended December 31, 2025. The filing includes a press release providing a business update alongside the financial data.
Key Facts
- Reported financial results for Q4 2025 and the full year ended December 31, 2025
- Filing date of March 5, 2026
- The information was furnished under Item 2.02 and is not deemed 'filed' for liability purposes
- Includes Exhibit 99.1: Press Release Issued by Caribou Biosciences, Inc. on March 5, 2026