- First allogeneic CAR-T cell therapy with PD-1 deleted by CRISPR genome editing cleared for Phase 1 clinical trials
- Upon initiation of the ANTLER Phase 1 clinical trial, CB-010 will be Caribou’s first clinical-stage product candidate
BERKELEY, Calif.–(BUSINESS WIRE)–Caribou Biosciences, Inc., a leading CRISPR genome editing company, announced today that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for CB-010, an off-the-shelf allogeneic anti-CD19, genome-edited CAR-T cell therapy for patients with relapsed/refractory B cell non-Hodgkin lymphoma (B-NHL).
Upon initiation of the ANTLER Phase 1 trial, CB-010 will be Caribou’s first clinical-stage product candidate. CB-010 is manufactured from healthy donor T cells using Caribou’s next-generation CRISPR genome editing technology. Through genome editing, PD-1 is deleted from the CAR-T cells, which in preclinical studies promoted an increase in the durability of antitumor activity. Genome editing is used to remove the endogenous T cell receptor in order to prevent graft-versus-host disease and to site-specifically insert the CAR into the CAR-T genome.
“We are excited to receive clearance for our first IND, a pivotal milestone in the continued evolution of Caribou,” said Rachel Haurwitz, Ph.D., Caribou’s President and Chief Executive Officer. “Caribou’s genome-edited cell therapies hold tremendous potential for patients and we are eager to begin clinical studies for CB-010.”
ANTLER is an open-label study designed to evaluate the safety and efficacy of a single dose of CB-010 in adult patients with different subtypes of relapsed/refractory B-NHL. The study will be conducted at multiple clinical trial sites in the United States, and enrollment is expected to begin later this year. (Read more…)
“B-NHL comprises multiple serious and life-threatening diseases, and CB-010 therapy has the potential to extend lives,“ said Steve Kanner, Ph.D., Caribou’s Chief Scientific Officer. “CB-010 is distinct among allogeneic CAR-Ts since the critical checkpoint PD-1 is eliminated to reduce CAR-T cell exhaustion, which we believe offers a crucial therapeutic advantage.”
About Caribou Biosciences, Inc.
Caribou is a leading company in CRISPR genome editing founded by pioneers of CRISPR biology. The company is developing an internal pipeline of off-the-shelf allogeneic CAR-T cell therapies and genome-edited natural killer (NK) cell therapies. For more information about Caribou visit www.cariboubio.com and follow the Company @CaribouBio.
“Caribou Biosciences” and the Caribou logo are registered trademarks of Caribou Biosciences, Inc.
Contacts
Caribou Biosciences Media Contact:
Greg Kelley
Ogilvy
gregory.kelley@ogilvy.com
(617)-461-4023