TrialSignal
Clinical trial intelligence report
A Phase 1, Multicenter, Open-Label Study of CB-012, a CRISPR-Edited Allogeneic Anti-CLL-1 CAR-T Cell Therapy in Patients With Relapsed/Refractory Acute Myeloid Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 20, 2026
NCT ID
NCT06128044
Status
TERMINATED
Phase
Phase 1
Sponsor
Caribou Biosciences, Inc.
Executive brief
Investment-Ready Snapshot
CB-012, developed by Caribou Biosciences, Inc., represents a novel allogeneic CAR-T cell therapy targeting CLL-1 for patients with relapsed/refractory acute myeloid leukemia (AML). The market for AML therapies is significant, with a growing demand for innovative treatments due to the high unmet need in this patient population. The competitive landscape includes established therapies and emerging CAR-T products. The termination of this trial due to pipeline reprioritization may indicate a strategic shift for Caribou, potentially reallocating resources to more promising assets. This decision could impact investor confidence and market positioning, necessitating close monitoring of Caribou's future developments and strategic focus.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06128044
Indication
Acute Myeloid Leukemia, in Relapse
Modality
cell therapy
Target
C-type lectin-like molecule-1 (CLL-1)
Intervention
CB-012
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.