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A Phase 3 Study to Evaluate the Efficacy, Safety, and Tolerability of VX-880 in Subjects With Type 1 Diabetes With a Kidney Transplant
This study will evaluate the efficacy, safety, and tolerability of VX-880 in participants with Type 1 Diabetes (TID) with a kidney transplant.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Perelman Center for Advanced Medicine - Endocrinology
Philadelphia, Pennsylvania, United States
Montefiore Clinical and Translational Research Center - Endocrinology
Pittsburgh, Pennsylvania, United States
UW University Hospital - Endocrinology
Madison, Wisconsin, United States
Toronto General Hospital - Endocrinology
Toronto, Canada
Vancouver General Hospital - Gordon and Leslie Diamond Health Care Centre
Vancouver, Canada
King Abdullah International Medical Research Center (KAIMRC) - Riyadh - Endocrinology
Riyadh, Saudi Arabia
King Faisal Specialist Hospital & Research Centre - Riyadh - Endocrinology
Riyadh, Saudi Arabia
Start Date
March 31, 2025
Primary Completion Date
September 17, 2026
Completion Date
September 17, 2027
Last Updated
August 21, 2025
10
ESTIMATED participants
Biological/Vaccine
BIOLOGICAL
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05188027