drugset / Trial / NCT05210530

An Open-Label, FIH Study Evaluating the Safety and Tolerability of VCTX210A Combination Product in Subjects With T1D

NCT05210530 ↗

Phase 1 Completed 7 enrolled CRISPR Therapeutics AG ViaCyte · collab
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multicenter, Phase 1 study evaluating the safety and tolerability of VCTX210A combination product in patients with T1D

Timeline

Start
2022-01-24
Primary completion
2023-01-19
Completion
2023-01-19

Drugs

EvaluationDrugModalityDoseRoute
Subject PEC210A Cell therapy — Other