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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03762512
Enrollment
300
Registered
2018-12-03
Start date
2018-12-01
Completion date
2028-03-31
Last updated
2025-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy Related

Brief summary

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

Interventions

None listed

Sponsors

Minovia Therapeutics Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Placenta donatedimmediateThe purpose of this study is to collect placenta for the production of mitochondria. Therefore, only general measurements are taken such as placenta weight and health of mother during pregnancy. No further intervention or interaction with the mother will occur, and she does not receive any drug product or treatment prior to or after placenta donation.

Countries

Israel

Contacts

Primary ContactKlari Uziel
klariuz@clalit.org.il+972544817280

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026