Pharmacokinetics and Pharmacodynamics of DMPA With HIV PrEP

EARLY_PHASE1CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

November 17, 2017

Primary Completion Date

April 18, 2018

Study Completion Date

December 1, 2020

Conditions
HIV/AIDSContraception
Interventions
COMBINATION_PRODUCT

tenofovir/emtricitabine

At the enrollment visit, participants will be given a 14-day supply of tenofovir/emtricitabine 200mg/300mg to take once daily for 14 days. Drug concentrations will be measured as outlined in the outcomes section at the end of the two week period. The tenofovir/emtricitabine 200mg/300mg course will be repeated approximately 2 to 6 weeks later to allow washout of tenofovir/emtricitabine.

DRUG

DMPA

After completion of the first 14 day course of tenofovir/emtricitabine depot medroxyprogesterone acetate 150 mg will be administered as intramuscular injection.

Trial Locations (1)

15213

Magee-Womens Hospital of UPMC, Pittsburgh

All Listed Sponsors
lead

Sharon Achilles

OTHER

NCT03197961 - Pharmacokinetics and Pharmacodynamics of DMPA With HIV PrEP | Biotech Hunter | Biotech Hunter