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A Safety, Tolerability, and Efficacy Study of VX-264 in Participants With Type 1 Diabetes
NCT05791201 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of the study is to evaluate the safety, tolerability, and efficacy of VX-264 in participants with type 1 diabetes (T1D).
Conditions Studied
Interventions
- DRUG VX-264
Study Locations (16)
Other
- University of Alberta, Edmonton — Edmonton
- Montreal Clinical Research Institute — Montreal
- Toronto General Hospital (TGH) — Toronto
- Vancouver General Hospital — Vancouver
- Dresden Center for Islet Transplantation — Dresden
- IRCCS Ospedale San Raffaele — Milan
- Leiden University — Leiden
- Hopiteaux Universitaires de Geneve — Geneva
- Churchill Hospital — Headington
- Royal Victoria Infirmary — Newcastle upon Tyne
Pennsylvania
- Hospital of the University of Pennsylvania — Philadelphia
- University of Pittsburgh Medical Center Montefiore — Pittsburgh
Florida
- UHealth Diabetes Research Institute — Miami
Illinois
- University of Chicago — Chicago
Massachusetts
- Massachusetts General Hospital — Boston
Wisconsin
- University of Wisconsin — Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 7 participants |
| Start Date | 2023-05-16 |
| Est. Completion | 2026-05-29 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05791201
The ClinicalTrials.gov registry entry for NCT05791201 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 7 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vertex Pharmaceuticals Incorporated, which has 82 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Type 1 Diabetes appearing as the primary indexed condition, and to 1 intervention — of which VX-264 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05791201 reports 16 study locations spanning 6 distinct geographic areas — top geographies include Other, Pennsylvania, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05791201 about?
NCT05791201 is a clinical study titled "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).
What is the current status of trial NCT05791201?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 7 participants. The study started on 2023-05-16. Estimated completion is 2026-05-29.
What conditions does trial NCT05791201 study?
This clinical trial studies the following conditions: Type 1 Diabetes. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05791201?
The interventions under investigation include: VX-264 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05791201?
This trial is sponsored by Vertex Pharmaceuticals Incorporated, which has 82 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05791201 being conducted?
This trial has 16 study locations across Florida, Illinois, Massachusetts, Pennsylvania, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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