drugset / Trial / NCT05565248

An Open-Label, FIH Study Evaluating the Safety, Tolerability, and Efficacy of VCTX211 Combination Product in Subjects With T1D

NCT05565248 ↗

Phase 1 Terminated 5 enrolled CRISPR Therapeutics AG ViaCyte · collab
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multicenter, Phase 1 study evaluating the Safety, Tolerability, and Efficacy of VCTX211 Combination Product in Subjects with T1D

Timeline

Start
2023-01-20
Primary completion
2025-08-08
Completion
2025-08-08

Outcome

Outcome not reported

Stopped: “Patients to be followed up in the VCTX-201 study”

Drugs

EvaluationDrugModalityDoseRoute
Subject VCTX211 Unknown — —