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Compound · clinical trials

Zimislecel clinical trials

Also listed in trial records as VX-880
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our USA, Canada, UK, Germany, France, Italy, Netherlands, Switzerland and Norway registers that name Zimislecel as an intervention. Synced 1 Oct 2026
2Current trials
2Recruiting now
1Lead sponsor
9Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Zimislecel is named as an intervention in 2 current clinical trials in our USA, Canada, UK, Germany, France, Italy, Netherlands, Switzerland and Norway registers. 2 are recruiting patients now. All registered phases are Phase 3. The lead sponsor is Vertex Pharmaceuticals Incorporated. The most-studied condition is Diabetes Mellitus, Type 1.

How Zimislecel works

All drug targets →
Diseases it has been tested for in clinical trials, by furthest phase
  • Type 1 diabetes mellitusPhase 3

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL5314904, CC BY-SA 3.0. The Guide to Pharmacology has no record of this medicine, so its targets rest on ChEMBL alone. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Trials by status

  • Recruiting2100%

Trials by phase

  • Phase 32100%
01

Clinical trials of Zimislecel

2 trials
StudyPhaseStatusLead sponsorRegisters
A Safety, Tolerability, and Efficacy Study of VX-880 and VX-017 in Participants With Type 1 Diabetes
NCT04786262 · ClinicalTrials.gov ↗ · Diabetes Mellitus, Type 1, Impaired Hypoglycemic Awareness, Severe Hypoglycemia
Phase 3 Recruiting Vertex Pharmaceuticals Incorporated UK, USA, Germany, France, Italy, Netherlands, Switzerland, Norway, Canada
An Efficacy, Safety, and Tolerability Study of VX-880 in Participants With Type 1 Diabetes With a Kidney Transplant
NCT06832410 · ClinicalTrials.gov ↗ · Type 1 Diabetes, Kidney Transplant
Phase 3 Recruiting Vertex Pharmaceuticals Incorporated USA, Canada

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Zimislecel

5 conditions
Diabetes Mellitus, Type 11Impaired Hypoglycemic Awareness1Severe Hypoglycemia1Type 1 Diabetes1Kidney Transplant1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Vertex Pharmaceuticals Incorporated2
04

By country register

RegisterTrialsRecruiting
Clinical trials in USA22
Clinical trials in Canada22
Clinical trials in UK11
Clinical trials in Germany11
Clinical trials in France11
Clinical trials in Italy11
Clinical trials in Netherlands11
Clinical trials in Switzerland11
Clinical trials in Norway11

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Zimislecel trials

How many clinical trials are testing Zimislecel?

2 current trials in our USA, Canada, UK, Germany, France, Italy, Netherlands, Switzerland and Norway registers name Zimislecel (also registered as VX-880) as a drug or biological intervention, as of the registry sync on 1 October 2026. Completed and withdrawn studies are not counted.

Are Zimislecel trials recruiting patients?

Yes. 2 of the 2 trials are recruiting: 2 with sites in USA, 2 with sites in Canada, 1 with sites in UK, 1 with sites in Germany, 1 with sites in France, 1 with sites in Italy, 1 with sites in Netherlands, 1 with sites in Switzerland and 1 with sites in Norway. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Zimislecel clinical trials?

The lead sponsor is Vertex Pharmaceuticals Incorporated. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Zimislecel works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Zimislecel works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Zimislecel (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 1 Oct 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.