drugset / Trial / NCT04786262

A Safety, Tolerability, and Efficacy Study of VX-880 in Participants With Type 1 Diabetes

NCT04786262 ↗

Phase 3 Recruiting 52 enrolled Vertex Pharmaceuticals Incorporated
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety, tolerability and efficacy of VX-880 infusion in participants with Type 1 diabetes (T1D) and impaired awareness of hypoglycemia (IAH) and severe hypoglycemia.

Timeline

Start
2021-03-29
Primary completion
2027-06-30
Completion
2030-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject VX-880 Cell therapy — Other