Switch From Nevirapine-based Regimen to Once a Day Rilpivirine/Emtricitabine/Tenofovir

NCT ID: NCT02104700

Last Updated: 2021-03-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 150 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-04-30
• Study Completion Date: 2016-07-31

Brief Summary

The study will be an open-label, pilot study in virologically suppressed patients comparing the efficacy, safety and tolerability of two Antiretroviral regimen strategies:

Arm A: "Immediate switch" Rilpivirine/Emtricitabine/Tenofovir (single tablet formulation (STF))at randomization

Arm B: "Delayed switch" Continue Nevirapine/Lamivudine/other Nucleoside reverse transcriptase inhibitor (NRTI)through 24 weeks then switch to STF of Rilpivirine/emtrictabine/tenofovir and followed through 48 weeks.

Detailed Description

The current study is designed to be the first study to compare a continued nevirapine-based regimen to a switch to the FDC of rilpivirine/emtricitabine/tenofovir. Rwanda is a model country for implementation of newer approaches to more innovative ART strategies with an excellent National HIV Treatment program in place but has limited experience with clinical trials and as with most African countries has no clinical experience with Rilpivirine in treating HIV infected adults. Done in collaboration with Rwanda Biomedical center.

Conditions

HIV

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Rilpivirine/Emtricitabine/Tenofovir

"Immediate switch": RILPIVIRINE/ EMTRICITABINE /TENOFOVIR FDC QDAY at randomization.

Group Type: ACTIVE_COMPARATOR

Rilpivirine/Emtricitabine/Tenofovir

Intervention Type: DRUG

Rilpivirine 25mg/Emtricitiabine 200mg/Tenofovir 300mg FDC qday

Nevirapine/Lamivudine/ plus other NNRTI

"Delayed switch": Continue NEVIRAPINE 200MG BID + LAMIVUDINE 300MG + OTHER NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR (NRTI) through 24 weeks then switch to RILPIVIRINE 25MG/ EMTRICITABINE 200MG/TENOFOVIR 300MG FDC QDAY and then follow through 48 weeks.

Group Type: ACTIVE_COMPARATOR

Rilpivirine/Emtricitabine/Tenofovir

Intervention Type: DRUG

Rilpivirine 25mg/Emtricitiabine 200mg/Tenofovir 300mg FDC qday

Interventions

Rilpivirine/Emtricitabine/Tenofovir

Rilpivirine 25mg/Emtricitiabine 200mg/Tenofovir 300mg FDC qday

Intervention Type: DRUG

Other Intervention Names

Complera

Eligibility Criteria

Inclusion Criteria

• HIV-1 infection, as documented by any licensed ELISA test kit and confirmed by Western blot at any time prior to study entry. A second antibody test by a method other than ELISA is acceptable as an alternative confirmatory test or a previous detectable HIV RNA level
• HIV RNA level below the limit of quantification of the viral load assay in use in-country within the last 12 months
• Screening HIV RNA level below the limit of quantification as defined by the local assay
• At least twelve months of stable first-line antiretroviral therapy consisting of nevirapine and 2 nRTIs approved by the Rwandan HIV Treatment guidelines. (No prior changes in ART are allowed)
• Enrolled in the Rwanda National ART Program with no in-country transfer within the program.
• Negative TB symptom screen or eligible based on algorithm outlined in
• Laboratory values obtained within 30 days prior to study entry:

• Hemoglobin greater than 8.0 g/dL
• Platelet count greater than 40,000/mm3
• AST (SGOT), ALT (SGPT), and alkaline phosphatase less than 5 X ULN
• Total bilirubin less than 2.5 x ULN
• Calculated creatinine clearance greater than 60 mL/min as estimated by the Cockcroft-Gault equation:

• Ability to meet the nutritional requirements for rilpivirine; largest meal should consist of at least 400 total kcals and 117 kcals of fat (13 grams) to be assessed at screening.
• For women of reproductive potential, negative serum or urine pregnancy test within 4 weeks of initiating study medications and a negative urine pregnancy test at the entry visit prior to randomization.
• "Women of reproductive potential" is defined as women who have not been post-menopausal for at least 24 consecutive months (i.e., who have had menses within the preceding 24 months) and have not undergone surgical sterilization (e.g., hysterectomy, bilateral oophorectomy, or tubal ligation).
• Age greater than18 years.
• Ability and willingness of subject to give informed consent.

Exclusion Criteria

• History of on-treatment virologic failure (defined as HIV RNA level greater than 200 copies/mL at or after 6 months of antiretroviral therapy)
• Any change in prior ART.
• Currently breastfeeding.
• Active tuberculosis.
• Serious illness requiring systemic treatment and/or hospitalization until candidate either completes therapy or is clinically stable on therapy, in the opinion of the site investigator, for at least 14 days prior to study entry.
• NOTE: Isolated cutaneous Kaposi's Sarcoma, oral candidiasis, vaginal candidiasis, mucocutaneous herpes simplex, and other non-serious illnesses (as judged by the site investigator) have no restriction.
• Known allergy/sensitivity to study drugs or their formulations.
• Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
• Requirement for any current medications that are prohibited with any study treatment.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Gilead Sciences

INDUSTRY

Sponsor Role: collaborator

Philip Grant

OTHER

Sponsor Role: lead

Responsible Party

Philip Grant

Associatge Professor of Medicine

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Andrew Zolopa, MD

Role: PRINCIPAL_INVESTIGATOR

Stanford University

Locations

Rwanda Military Hospital

Kinombe, , Rwanda

Countries

Rwanda

Other Identifiers

ISR-In-US-264-0123

Identifier Type: OTHER

Identifier Source: secondary_id

Near Rwanda

Identifier Type: -

Identifier Source: org_study_id