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Collection of Donated Placenta for Isolation of Mitochondria for Research and for Future Use in Mitochondrial Augmentation Therapies

M

Minovia

Status

Enrolling

Conditions

Pregnancy Related

Study type

Observational

Funder types

Industry

Identifiers

NCT03762512
MNV-005

Details and patient eligibility

About

Placenta will be collected and from these, mitochondrial will be harvested. Mitochondria will be used in mitochondrial augmentation therapy.

Enrollment

300 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Healthy pregnant females between the age of 18-45, judged to be medically eligible by the Investigator and the Sponsor's Medical Monitor.
  2. Planned elective C-section at weeks 36-41 of pregnancy.
  3. Uncomplicated pregnancy as determined by the Investigator.
  4. Available Medical History of the donor (diagnosis, diseases, medication etc...)

Exclusion criteria

  1. Donor is positive for a communicable disease, such as: HBV, HCV, HIV 1&2, WNV, HTLV 1&2, Treponema pallidum, CMV, Chagas, Chlamydia Trachomatis, Neisseria Gonorrhea, or any other tests required by the medical facility, IMoH, FDA, EMA or the Sponsor.
  2. Donor is at risk for a communicable disease as assessed by medical history, medical records, physical exam, and the Donor Screening Questionnaire.
  3. Donor is at risk for COVID-19 as assessed by medical history, medical records, physical exam, and the COVID-19 Screening Questionnaire.
  4. Donor smokes more than one pack of cigarettes a day or drinks more than one alcoholic beverage a day.
  5. Donor has taken a medication with potential mitochondrial effects within 2 weeks prior to placental donation, such as valproic acid, aminoglycoside antibiotics, neuromuscular blocking drugs (See Appendix 3).
  6. Donor has current or history of malignancy.
  7. Donor has current or history of insulin dependent diabetes
  8. Donor has current gestational diabetes treated with insulin, or pre-eclampsia.
  9. Donor is known to be a carrier of a primary mitochondrial disease.

Trial contacts and locations

1

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Central trial contact

Klari Uziel

Data sourced from clinicaltrials.gov

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