Maternal TDF and FTC to Reduce NNRTI Resistance Mutations After Intrapartum NVP

HIV Clinical Trial

— TD-2  

Official title:

Addition of Single-dose, Maternal Tenofovir and Emtricitabine to Reduce Non-nucleoside Reverse Transcriptase Inhibitor Resistance Mutations in the Setting of Zidovudine and Nevirapine for Prevention of Mother-to-child HIV Transmission

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00204308
• Other study ID #: EGSA 19-02
• Status: Completed
• Phase: Phase 2
• First received: September 12, 2005
• Last updated: May 30, 2012
• Start date: March 2005
• Est. completion date: May 2007

Study information

• Verified date: May 2012
• Source: University of North Carolina, Chapel Hill
• Contact: n/a
• Is FDA regulated: No
• Health authority: Zambia: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether the addition of tenofovir (TDF) and emtricitabine (FTC)to a standard PMTCT regimen containing single-dose nevirapine (NVP) can reduce the development of post-ingestion HIV resistance to non-nucleoside reverse transcriptase inhibitors (NNRTIs).

Description:

Single-dose intrapartum and neonatal nevirapine (NVP), either alone or in combination with short course zidovudine (ZDV) is in widespread use to prevent mother-to-child HIV transmission throughout the developing world. Though the public health benefits cannot be overstated, widespread use of NVP in this fashion may come at a cost. Non-nucleoside reverse transcriptase inhibitor (NNRTI) resistance mutations are induced in at least 20% and probably a larger proportion of women exposed to NVP in this fashion. Addition of short-course ZDV does not appear to mitigate this effect substantially. The full implications of these NVP resistance mutations are yet unknown, though there is concern that they may result in reduced efficacy of the NVP or other NNRTIs in long-term, therapeutic regimens.

We are conducting a clinical trial of tenofovir (TDF) and emtricitabine (FTC), marketed as a fixed dose combination, Truvada ™, to reduce NNRTI-resistance post-delivery in the setting of NVP with or without ZDV for PMTCT. TDF and FTC are both Category B drugs and are approved for use in pregnancy. They have several characteristics that make them ideal candidate drugs for use in conjunction with NVP, including long intracellular half-lives and established safety profile among adults for HIV treatment.

Women will be enrolled between 28 and 38 weeks of gestation. As part of normal PMTCT services, they may choose NVP-boosted ZDV or single dose NVP for PMTCT; We anticipate that most (~80%) will choose the former. At arrival for delivery, they will be randomized to receive either the two study drugs (intervention) or no drug (control). A total of 400 women will be randomized, and followed, along with their infants, for 6 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 400
• Est. completion date: May 2007
• Est. primary completion date: May 2007
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 16 Years and older

Eligibility

Inclusion Criteria:

• Serologically confirmed HIV infection;

• Gestational age of 28 to 38 weeks;

• Previous selection of a NVP-based PMTCT regimen (with or without ZDV)

• Willingness to participate in a randomized trial;

• Willingness to follow up in a postpartum visit schedule;

• Willingness to allow her infant to participate in this trial;

Exclusion Criteria:

• Use of antiretroviral medications before this pregnancy, even in a single dose.

• Current use of antiretroviral medications for treatment of advanced HIV disease and/or AIDS

• Illness or complication of pregnancy likely to warrant transfer to the University Teaching Hospital (UTH), known at time of randomization;

• Known or suspected allergy to NVP or other benzodiazepine medications;

• History of known liver disease.

• Hemoglobin level of 7.9 g/dL or less

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

• HIV
• Pregnancy

Intervention

Drug:
• Combination tenofovir-emtricitabine
Tenofovir disoproxil 300 mg / emtricitabine 200 mg taken as a single dose during labor

Locations

Country	Name	City	State
Zambia	Kalingalinga Health Centre	Lusaka
Zambia	Kanyama Health Centre	Lusaka

Sponsors (2)

Lead Sponsor	Collaborator
University of North Carolina, Chapel Hill	Elizabeth Glaser Pediatric AIDS Foundation

Country where clinical trial is conducted

Zambia, 

References & Publications (4)

Chi BH, Chintu N, Cantrell RA, Kankasa C, Kruse G, Mbewe F, Sinkala M, Smith PJ, Stringer EM, Stringer JS. Addition of single-dose tenofovir and emtricitabine to intrapartum nevirapine to reduce perinatal HIV transmission. J Acquir Immune Defic Syndr. 200 — View Citation

Chi BH, Ellis GM, Chintu N, Cantrell RA, Sinkala M, Aldrovandi GM, Warrier R, Mbewe F, Nakamura K, Stringer EM, Frenkel LM, Stringer JS. Intrapartum tenofovir and emtricitabine reduces low-concentration drug resistance selected by single-dose nevirapine f — View Citation

Chi BH, Sinkala M, Mbewe F, Cantrell RA, Kruse G, Chintu N, Aldrovandi GM, Stringer EM, Kankasa C, Safrit JT, Stringer JS. Single-dose tenofovir and emtricitabine for reduction of viral resistance to non-nucleoside reverse transcriptase inhibitor drugs in — View Citation

Dorton BJ, Mulindwa J, Li MS, Chintu NT, Chibwesha CJ, Mbewe F, Frenkel LM, Stringer JS, Chi BH. CD4+ cell count and risk for antiretroviral drug resistance among women using peripartum nevirapine for perinatal HIV prevention. BJOG. 2011 Mar;118(4):495-9. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	maternal antiretroviral drug resistance to non-nucloeoside reverse transcriptase inhibitors		6 weeks	No
Secondary	maternal antiretroviral drug resistance to non-nucloeoside reverse transcriptase inhibitors		2 weeks	No
Secondary	maternal hematological and renal function after TDF-FTC use		6 weeks	Yes