Recruiting
Phase 1, Phase 2
A Safety, Tolerability, and Efficacy Study of VX-264 in Participants With Type 1 Diabetes

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

ClinicalTrials.gov Identifier

Eligibility criteria
Sex
Age
18 Years - 65 Years
Phase
1, 2
Key inclusion criteria
  • * Clinical history of T1D with greater than or equal to (\>=) 5 years duration
  • * Participant is on a stable diabetic treatment
  • * Consistent use of continuous glucose monitoring (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, or cell therapy
Other protocol defined Inclusion/Exclusion criteria may apply.
Trial details
Condition
Type 1 Diabetes
Study duration
May 2023 - May 2026
Study type
Interventional
Intervention/Treatment
DRUG : VX-264
Estimated enrollment
17

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About clinical trials

Volunteers who participate in clinical trials help make new medicines a reality. Clinical trials are carefully designed research studies in humans that evaluate the safety and efficacy of an investigational medicine.

If you’re interested in participating in a Vertex clinical trial, we encourage you to speak with your health care provider first about what’s involved and your eligibility. 

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