Caribou Biosciences, Inc. (CRBU), a clinical-stage CRISPR genome-editing biopharmaceutical company, said it will discontinue development of two allogeneic CAR-T cell therapy programs: vispa-cel for relapsed or refractory B-cell non-Hodgkin lymphoma and CB-011 for relapsed or refractory multiple myeloma.
Vispa-cel had reached pivotal-trial readiness, and the company had already agreed with the FDA on a Phase 3 trial design.
The company will also discontinue clinical development and significantly reduce its workforce, with most layoffs expected by the fourth quarter of 2026.
Caribou cited a challenging financing environment for allogeneic CAR-T therapies that has made it increasingly difficult to raise the capital needed to advance these programs. Consequently, it plans to evaluate strategic alternatives.
Its Board of Directors approved a strategic review process that may include a merger, acquisition, business combination, or other transactions involving the company or its assets.
Wedbush Securities has been retained as the company’s exclusive financial adviser for the review.
Caribou has not established a timeline for completing the strategic review.
As of June 30, 2026, the company had $113.8 million in cash, cash equivalents, and marketable securities.
CRBU shares have traded between $1.13 and $3.53 over the past year. The stock closed Tuesday at $1.13, down 4.62%, and fell 39.49% to $0.68 in overnight trading.
Also Read
- Stockholm to Host Nobel Chemistry Prize Ceremony
- Navigating the Trump Tightrope: Republican Candidates Face a Delicate Political Balance
- Bahrain Foreign Minister Arrives in Islamabad to Advance Trade, Security and Investment Ties
- IDF Unveils Three-Year War Report: Near 100,000 Targets Struck and Command Restructuring Detailed

