drugset / Trial / NCT05061030

Mesenchymal Stromal Cells to Treat Type 1 Diabetes in Children and Adolescents

NCT05061030 ↗

Phase 1/2 Active not recruiting 66 enrolled Uppsala University Hospital
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a combined phase 1 and 2 study in 66 subjects, male or female, between 7-21 years of age that have recently (\< 6 months) been diagnosed with type 1 diabetes. The first phase 1 part of the study includes six subjects openly receiving allogeneic Wharton's jelly derived mesenchymal stromal cells as the Advanced Therapy Medicinal Product (ATMP) Protrans, three each in the age ranges 7-11 and 12-18.The second part is a randomized, double-blinded placebo-controlled phase 2 study in parallel design comparing allogeneic Wharton's jelly derived mesenchymal stromal cells treatment (as Protrans) to placebo in children and adolescent subjects (7-21 years of age) diagnosed with type 1 diabetes, The primary objectives of this study will be to investigate the safety, tolerance and efficacy after an allogieneic infusion of Wharton's jelly derived mesenchymal stromal cells.

Timeline

Start
2022-01-14
Primary completion
2028-09
Completion
2028-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator ProTrans Cell therapy 1e+08 cells Intravenous
Comparator ProTrans Cell therapy 2e+08 cells Intravenous