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TerminatedPhase 1

An Open-Label, FIH Study Evaluating the Safety, Tolerability, and Efficacy of VCTX211 Combination Product in Subjects With T1D

Key facts

Who runs it
CRISPR Therapeutics AG
Where
Canada2 sites in 1 countryChoose a country to see its sites
Trial code
Status
Terminated
Phase
Phase 1
People taking part
5 people enrolled
Started
20 Jan 2023
Ended
8 Aug 2025
Type of study
Interventional
Treatments tested
  • VCTX211
Record updated
7 May 2026
Why it stopped
Patients to be followed up in the VCTX-201 study

Who can take part

Age
18 years to 65 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 7 criteriaShow less

Who can take part

  • Diagnosis of T1D for a minimum of 5 years
  • Stable diabetes regimen for at least 3 months prior to enrollment

Who cannot take part

  • Occurrence of 2 or more severe, unexplained hypoglycemic events within 6 months prior to enrollment
  • Immunosuppressant therapy in the previous 30 days and/or requirements for chronic immunosuppressive therapy during the study
  • Prior treatment with gene therapy or edited product
  • Medical history of islet cell, kidney, and/or pancreas transplant
  • Known causes of diabetes other than T1D

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

This is an open-label, multicenter, Phase 1 study evaluating the Safety, Tolerability, and Efficacy of VCTX211 Combination Product in Subjects with T1D

The group in the trial

  • VCTX211 unitTreatment being tested

    Treatment: VCTX211

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
An Open-Label, First-in-Human Study Evaluating the Safety, Tolerability, and Efficacy of VCTX211 Combination Product in Subjects With Type 1 Diabetes Mellitus (T1D)
Publications
Record updated
7 May 2026