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A Phase 1 Dose Escalation and Cohort Expansion Study of the Safety and Efficacy of Anti-BCMA Allogeneic CRISPR-Cas9-Engineered T Cells (CTX120) in Subjects With Relapsed or Refractory Multiple Myeloma
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 25, 2026
Report code
NCT04244656-Jun 25, 2026
NCT ID
NCT04244656
Status
TERMINATED
Phase
Phase 1
Sponsor
CRISPR Therapeutics AG
Executive brief
Investment-Ready Snapshot
CRISPR Therapeutics AG is advancing CTX120, an allogeneic CRISPR-Cas9-engineered T cell therapy targeting BCMA, for the treatment of relapsed or refractory multiple myeloma. The therapy is positioned within a competitive landscape that includes CAR T-cell therapies and other BCMA-targeted treatments. Given the increasing prevalence of multiple myeloma and the limitations of existing therapies, CTX120 has the potential to capture significant market share, particularly if it demonstrates a favorable safety and efficacy profile. The termination of the trial indicates a strategic pivot to follow-up studies, suggesting ongoing commitment to this asset's development and potential future commercialization.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04244656
Indication
Multiple Myeloma
Modality
gene therapy
Target
B-cell maturation antigen (BCMA)
Intervention
CTX120
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.