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
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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 ColumbiaVancouver, British Columbia
Canada
Contactez l'équipe d'étude
Study Coordinator
University of Alberta
University of AlbertaEdmonton, Alberta
Canada
Contactez l'équipe d'étude
- Étude parrainée par
- CRISPR Therapeutics
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT05565248