Darunavir and Rilpivirine Interactions With Etonogestrel Contraceptive Implant

HIV Clinical Trial

— DRIVE-1  

Official title:

A Pharmacokinetic Evaluation of Etonogestrel Implant in HIV-infected Women on Darunavir Versus Ripilvirine-based Antiretroviral Therapy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03589040
• Other study ID #: PK21
• Status: Recruiting
• Phase: Phase 2
• Start date: September 25, 2018
• Est. completion date: June 2020

Study information

• Verified date: March 2019
• Source: Makerere University
• Contact: Senior research administrator
• Phone: 0392878652
• Email: sokoboi[@]idi.co.ug
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will evaluate the pharmacokinetic properties of rilpivirine and darunavir when used in combination with etonogestrel

Description:

Despite the benefits of hormonal contraceptives, significant drug-drug interactions (DDIs) with some antiretroviral therapies (ART) represent a barrier to effective family planning methods for HIV-infected women. It is therefore critical to generate data on the combined use of hormonal contraceptives and ART. This study is a prospective, non-randomized, open-label, parallel, two-group, sparse-sampling pharmacokinetic study to describe etonogestrel (ENG) pharmacokinetic (PK) parameters in two treatment groups (rilpivirine or darunavir- based ART) in 60 HIV-1 infected women. The primary endpoint is the comparison of the mean ENG concentrations at month 6 between the rilpivirine or darunavir treatment groups versus historical controls. This study will provide information on effective ART options for HIV positive women who opt for the contraceptive implant as a family planning method of choice.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: June 2020
• Est. primary completion date: June 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Evidence of a personally signed and dated informed consent document indicating that the participant has been informed of all pertinent aspects of the study.

2. Participants who are willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.

3. Women age 18 years to 45 years

4. Diagnosed with HIV infection

5. Medically eligible for the ENG subdermal implant as a contraceptive method based on the WHO Medical Eligibility Criteria for Contraceptive Use

6. Receiving EFV- or LPV/r-based ART for a minimum of 1 year

7. If not abstinent, must agree to use an effective non-hormonal method of contraception for the duration of the study including male and female condoms or the copper-T intrauterine device.

8. Participants must have a negative urine pregnancy test at entry and report no unprotected sex since the last menstrual period or in the last two weeks.

Exclusion Criteria:

1. HIV RNA greater than 50 copies/mL at the screening visit

2. CD4 count below 200 cells/mm3 at the screening visit

3. History of virologic failure on the current regimen (two consecutive viral load results equal to or greater than 400 copies/mL)

4. Serum hemoglobin less than 9.0 g/dl at screening

5. Elevations in serum levels of alanine transaminase (ALT) above 5 times the upper limit of normal

6. Elevations in serum creatinine above 2.5 times the upper limit of normal

7. Use of drugs known to be contraindicated with ENG, RPV (for women taking EFV-based ART), or DRV (for women taking LPV-based ART) within 30 days of study entry. Due to the dynamic nature of drug interactions related to antiretroviral therapy, the study team will review all concomitant medications at screening based on the US Department of Health and Human Services drug interaction table and the University of Liverpool HIV drug interaction tables (www.hiv-druginteractions.org)

8. Currently pregnant or postpartum <30 days at study entry.

9. Breastfeeding women within 6 months of delivery.

10. Patients with a history of hypersensitivity to ENG implant, undiagnosed vaginal bleeding, diagnosed or suspected sex hormone dependent neoplasia, benign or malignant liver tumor, or thromboembolic disease.

11. Presence of any active clinically significant disease or life-threatening disease that, in the investigator's opinion, would compromise the subject's safety or outcome of the study.

Related Conditions & MeSH terms

• Contraception
• HIV

Intervention

Drug:
• Etonogestrel 68Mg Implant
Etonogestrel single-rod subdermal implant (68mg/rod) will be administered to all study participants
• rilpivirine
Oral rilpvirine 25mg
• darunavir
Oral darunavir+ritonavir 600/100mg

Locations

Country	Name	City	State
Uganda	Infectious Diseases Institue	Kampala

Sponsors (4)

Lead Sponsor	Collaborator
Makerere University	University of Liverpool, University of Nebraska, University of Pittsburgh

Country where clinical trial is conducted

Uganda, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Concentration of etonogestrel	Comparison of the mean etonogestrel concentrations at month 6 between rilpivirine and darunavir treatment groups versus historical controls.	Six months of combined use.
Secondary	Concentration of rilpivirine and darunavir	Rilpivirine and darunavir mean concentration changes prior to implant placement and then over the duration of the study time period.	12 months
Secondary	Number and severity of adverse events	Any signs and symptoms related to hormone exposure, including abnormal vaginal bleeding and local or systemic adverse events observed during the study period in both study groups.	12 months