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ACTIVE NOT RECRUITING
NCT05791201
PHASE1/PHASE2

A Safety, Tolerability, and Efficacy Study of VX-264 in Participants With Type 1 Diabetes

Sponsor: Vertex Pharmaceuticals Incorporated

View on ClinicalTrials.gov

Summary

The purpose of the study is to evaluate the safety, tolerability, and efficacy of VX-264 in participants with type 1 diabetes (T1D).

Official title: A Phase 1/2 Study to Evaluate the Safety, Tolerability, and Efficacy of VX-264 in Subjects With Type 1 Diabetes Mellitus

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

7

Start Date

2023-05-16

Completion Date

2026-05-29

Last Updated

2025-08-11

Healthy Volunteers

No

Conditions

Interventions

DRUG

VX-264

Allogeneic human stem cell-derived islets.

Locations (16)

UHealth Diabetes Research Institute

Miami, Florida, United States

University of Chicago

Chicago, Illinois, United States

Massachusetts General Hospital

Boston, Massachusetts, United States

Hospital of the University of Pennsylvania

Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center Montefiore

Pittsburgh, Pennsylvania, United States

University of Wisconsin

Madison, Wisconsin, United States

University of Alberta, Edmonton

Edmonton, Canada

Montreal Clinical Research Institute

Montreal, Canada

Toronto General Hospital (TGH)

Toronto, Canada

Vancouver General Hospital

Vancouver, Canada

Dresden Center for Islet Transplantation

Dresden, Germany

IRCCS Ospedale San Raffaele

Milan, Italy

Leiden University

Leiden, Netherlands

Hopiteaux Universitaires de Geneve

Geneva, Switzerland

Churchill Hospital

Headington, United Kingdom

Royal Victoria Infirmary

Newcastle upon Tyne, United Kingdom