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Clinical Trials/NCT06017869
NCT06017869
Recruiting
Phase 2

PHASE II, OPEN LABEL, SINGLE DOSE STUDY OF THE SAFETY AND EFFICACY OF MNV-201 FOR THE TREATMENT OF PEARSON SYNDROME

Minovia Therapeutics Ltd.1 site in 1 country6 target enrollmentJuly 31, 2023

Overview

Phase
Phase 2
Intervention
MNV-201
Conditions
Mitochondrial Diseases
Sponsor
Minovia Therapeutics Ltd.
Enrollment
6
Locations
1
Primary Endpoint
Occurrence of treatment-related adverse events
Status
Recruiting
Last Updated
10 months ago

Overview

Brief Summary

Primary Mitochondrial diseases are a clinically and genetically heterogeneous group of disorders caused by mutations in genes encoded by nuclear Deoxyribonucleic Acid (DNA) or by mutations and/or deletions in the mitochondrial DNA (mtDNA). While some mitochondrial disorders only affect a single organ (e.g., the eye in Leber hereditary optic neuropathy [LHON]), many involve multiple organs. Mitochondrial disorders may present at any age and a frequent feature is the increasing number of organs involved in the course of the disease.

Minovia Therapeutics Ltd. ("Minovia") is a biotech company developing novel therapeutics based on its mitochondrial augmentation technology (MAT). MNV-201 is a cell therapy produced by MAT that consists of the participant's autologous CD34+ hematopoietic stem and progenitor cells (HSPCs) enriched with allogeneic placental-derived mitochondria, manufactured in Minovia's GMP facility.

Registry
clinicaltrials.gov
Start Date
July 31, 2023
End Date
December 1, 2027
Last Updated
10 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female participants aged from 1 to 18 years old.
  • Diagnosis of Pearson Syndrome (current or history) as verified by molecular identification of deletion in mtDNA of peripheral blood. Participants are diagnosed with PS Participant can be in either the PS manifestations of the disease or may have transitioned to Kearns Sayre Syndrome (KSS) manifestations but has a history of PS.
  • Participants have failure to thrive (height SDS smaller than -1)
  • Participants should have at least 12 months' history of body weight and height and calculated GFR (from creatinine) before treatment.
  • Body weight ≥ 10 kg.
  • Participants' living parent(s) and/or legal guardian(s) able to understand and provide voluntary written informed consent.
  • Participants' parents or legal guardian have a good understanding of the study and nature of the procedure and are expected to be able to comply with study visit schedules and caregiver assessments without difficulty.
  • Participants' parents or legal guardian provides written informed consent prior to study participation.
  • Participants are medically able to undergo the study interventions as determined by the Investigator.
  • Exclusion criteria:

Exclusion Criteria

  • Not provided

Arms & Interventions

Autologous CD34+ cells enriched with allogenic placenta-derived mitochondria

Intervention: MNV-201

Outcomes

Primary Outcomes

Occurrence of treatment-related adverse events

Time Frame: 12 months post treatment.

Occurrence of treatment-related adverse events as assessed by CTCAE v5.0 following MNV-201 infusion

Height SDS

Time Frame: 24 months

Improvement from baseline to 12 months post treatment in height SDS compared to the calculated change in height SDS in the 12 months prior to treatment.

Secondary Outcomes

  • Height SDS(12 months)
  • Calculated GFR Slope(24 months)

Study Sites (1)

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