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NCT06128044TERMINATEDanonymous

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

Sponsor

Source record

Caribou Biosciences, Inc.

Phase

Source record

Phase 1

Modality

AI-normalized

cell therapy

Target

AI-normalized

C-type lectin-like molecule-1 (CLL-1)

Indication / condition

AI-normalized

Acute Myeloid Leukemia, in Relapse

Intervention

Source record

CB-012

Source & freshness

Source record

NCT ID

NCT06128044

Original source

ClinicalTrials.gov

Source last updated

Jun 11, 2025

Ingested at

Jun 12, 2026

Internal sync

Jun 12, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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View original source fields

NCT ID

NCT06128044

Title

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

Sponsor

Caribou Biosciences, Inc.

Status

TERMINATED

Phase

Phase 1

Condition raw

Acute Myeloid Leukemia, in Relapse, Acute Myeloid Leukemia Refractory

Condition normalized

Acute Myeloid Leukemia, in Relapse, Acute Myeloid Leukemia Refractory

Modality raw

cell therapy

Modality normalized

cell therapy

Target raw

C-type lectin-like molecule-1 (CLL-1)

Target normalized

C-type lectin-like molecule-1 (CLL-1)

Interventions

CB-012

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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