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

Diabetes Mellitus, Type 1 | Endocrine System Diseases | Autoimmune Diseases | Diabetes...

This is an open-label, multicenter, Phase 1/2 study evaluating the Safety, Tolerability, and Efficacy of VCTX211 Combination Product in Subjects with T1D

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 to 65

Critères de participation

Inclusion Criteria:

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

Exclusion Criteria:

* Medical history of islet cell, kidney, and/or pancreas transplant
* Occurrence of 2 or more severe, unexplained hypoglycemic events within 6 months prior to enrollment
* Known causes of diabetes other than T1D
* 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

Lieu de l'étude

University of British Columbia
University of British Columbia
Vancouver, British Columbia
Canada

Contactez l'équipe d'étude

Primary Contact

Study Coordinator

University of Alberta
University of Alberta
Edmonton, Alberta
Canada

Contactez l'équipe d'étude

Primary Contact

Sara Qureshi

[email protected]
Étude parrainée par
CRISPR Therapeutics
Participants recherchés
Plus d'informations
ID de l'étude: NCT05565248