A Safety and Efficacy Study Evaluating CTX130 in Subjects With Relapsed or Refractory Renal Cell Carcinoma
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- STATUS
- Recruiting
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- End date
- Apr 5, 2027
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- participants needed
- 95
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- sponsor
- CRISPR Therapeutics AG
Summary
This is a single-arm, open-label, multicenter, Phase 1 study evaluating the safety and efficacy of CTX130 in subjects with relapsed or refractory renal cell carcinoma.
Description
The study may enroll approximately 95 subjects in total.
Details
| Condition | Adenocarcinoma, Adenocarcinoma, Malignant neoplasm of kidney, kidney cancer, Renal Cell Carcinoma, Renal Cell Carcinoma, renal cell cancer, kidney cancer, renal cell cancer |
|---|---|
| Age | 18years - 100years |
| Treatment | CTX130 |
| Clinical Study Identifier | NCT04438083 |
| Sponsor | CRISPR Therapeutics AG |
| Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
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Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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