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A Phase 1 Dose Escalation and Cohort Expansion Study of the Safety and Efficacy of Allogeneic CRISPR-Cas9-Engineered T Cells (CTX130) in Subjects With Advanced, Relapsed or Refractory Renal Cell Carcinoma With Clear Cell Differentiation
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT04438083-Aug 04, 2026
NCT ID
NCT04438083
Status
TERMINATED
Phase
Phase 1
Sponsor
CRISPR Therapeutics AG
Executive brief
Investment-Ready Snapshot
CRISPR Therapeutics AG's CTX130 is positioned in the competitive landscape of advanced renal cell carcinoma (RCC) therapies, particularly targeting patients with relapsed or refractory clear cell RCC. The market for RCC treatments is expanding, driven by the increasing incidence of the disease and the demand for innovative therapies. CTX130's unique mechanism of action through CRISPR-Cas9 technology may provide a competitive edge, particularly in a market where CAR T-cell therapies are gaining traction. However, the termination of this trial suggests potential challenges in achieving clinical endpoints or safety profiles, necessitating further diligence on the implications for future development and market entry.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04438083
Indication
Renal Cell Carcinoma
Modality
gene therapy
Target
CD70-directed T-cell immunotherapy utilizing CRISPR-Cas9 gene editing technology.
Intervention
CTX130
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.