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An Efficacy, Safety, and Tolerability Study of VX-880 in Participants With Type 1 Diabetes With a Kidney Transplant

RecruitingPhase 3Ages 18 Years - 65 YearsAllVertex Pharmaceuticals Incorporated
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In plain words

What the trial is, and whether it could suit you

This study will evaluate the efficacy, safety, and tolerability of VX-880 in participants with Type 1 Diabetes (TID) with a kidney transplant.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Key Inclusion Criteria: * Clinical history of T1D with greater than or equal to (โ‰ฅ)5 years of insulin dependence * Taking a stable immunosuppression regimen of tacrolimus and mycophenolate mofetil, mycophenolate sodium, or sirolimus for at least 4 weeks * Consistent use of continuous glucose monitor (CGM) for at least 4 weeks before Screening and willingness to use CGM for the duration of the study Key Exclusion Criteria: * Prior islet cell transplant, organ transplant (other than kidney transplant), or cell therapy, except prior pancreatic graft that failed within the first 4 weeks * Participants had \>1 kidney transplant procedure Other protocol defined Inclusion/Exclusion criteria may apply.
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What it tests

  • Biological/Vaccine
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Where

7 sites
Perelman Center for Advanced Medicine - Endocrinology
Philadelphia, United States
Montefiore Clinical and Translational Research Center - Endocrinology
Pittsburgh, United States
UW University Hospital - Endocrinology
Madison, 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
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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