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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 13, 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., is an allogeneic CAR-T cell therapy targeting CLL-1, specifically designed for patients with relapsed or refractory acute myeloid leukemia (AML). The therapy aims to address a significant unmet need in the AML market, particularly for patients who have limited treatment options after multiple lines of therapy. The competitive landscape includes other CAR-T therapies and emerging treatments targeting similar patient populations. However, the unique CRISPR-editing technology may provide a differentiation point in terms of efficacy and safety profile. The termination of this trial due to sponsor decision and pipeline reprioritization raises concerns regarding the asset's future and may indicate a strategic shift within Caribou's portfolio, necessitating further diligence on their remaining assets and overall pipeline strategy.
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.