drugset / Trial / NCT04548843

A First in Human Study to Evaluate the Safety of Infusion of MNV-BM-PLC (Autologous CD34+ Cells Enriched With Placenta Derived Allogeneic Mitochondria) in Patients With Primary Mitochondrial Diseases Associated With Mitochondrial DNA Mutation or Deletion

NCT04548843 ↗

Phase 1 Withdrawn Minovia Therapeutics Ltd.
NaSequentialOpen-labelTreatment

Summary

The study objectives are to evaluate the safety of a single intravenous (IV) infusion of autologous CD34+ cells enriched with placenta-derived allogeneic mitochondria in participant with primary mitochondrial disease associated with mitochondrial DNA mutations or deletions. 6 participants aged from 4 to 18 years old on the day of screening visit with primary mitochondrial disease associated with mitochondrial DNA mutations or deletions will be enrolled.

Timeline

Start
2022-03-01
Primary completion
2024-12-01
Completion
2024-12-01

Outcome

Outcome not reported

Stopped (Enrollment): “No recruitment”

Drugs

EvaluationDrugModalityDoseRoute
Subject MNV-BM-PLC Cell therapy 0.88 unknown Intravenous
Subject MNV-BM-PLC Cell therapy 4.4 unknown Intravenous

Indications