An Open-Label, FIH Study Evaluating the Safety, Tolerability, and Efficacy of VCTX211 Combination Product in Subjects With T1D
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT05565248 |
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Recruitment Status :
Recruiting
First Posted : October 4, 2022
Last Update Posted : March 15, 2023
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Sponsor:
CRISPR Therapeutics AG
Collaborator:
ViaCyte
Information provided by (Responsible Party):
CRISPR Therapeutics ( CRISPR Therapeutics AG )
- Study Details
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- No Results Posted
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No Study Results Posted on ClinicalTrials.gov for this Study
| Recruitment Status : | Recruiting |
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| Estimated Primary Completion Date : | April 2025 |
| Estimated Study Completion Date : | August 2025 |