The Safety of Nevirapine When Given to Breast-Feeding Babies From Birth to Age 6 Months

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
National Institute of Allergy and Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier:
NCT00006279
First received: September 14, 2000
Last updated: February 13, 2012
Last verified: February 2012

September 14, 2000
February 13, 2012
Not Provided
Not Provided
Not Provided
Not Provided
Complete list of historical versions of study NCT00006279 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
The Safety of Nevirapine When Given to Breast-Feeding Babies From Birth to Age 6 Months
Phase I/II Study to Assess the Safety and Plasma Concentrations of Nevirapine Given Daily, Twice a Week or Weekly as Prophylaxis in Breastfeeding Infants From Birth to 6 Months

The purpose of this study is to see if it is safe to give nevirapine (NVP) to breast-feeding babies from birth to the age of 6 months and to determine what dose of NVP should be given.

Breast-feeding has been shown to be very important for the physical and mental health of infants. This is especially true during the first 6 months of life. However, an HIV-positive mother can pass the virus on to her baby by breast-feeding. Because of this risk, HIV-positive mothers are encouraged to formula-feed, not breast-feed, their babies. In developing countries, however, some women cannot afford to formula-feed. If they do formula-feed, these women risk exposing their HIV status. These women have great need for methods that can lower the chance that they will pass HIV on to their babies. This study will test NVP as a way of doing this.

Breast-feeding is of such critical importance to the general health of the infant, as well as the mother-infant relationship, that special efforts should be made to retain this practice even during the HIV pandemic. Breast-feeding is associated with lower rates of infant gastrointestinal infections and protects against high infant mortality from respiratory and gastrointestinal diseases. These protective effects are greatest in the first 6 months of life. However, HIV is transmitted through breast-feeding. HIV-infected women whose circumstances permit them a choice between breast- and formula-feeding have been encouraged to formula-feed. But in developing countries there are HIV-infected women who cannot afford to formula-feed or who, knowing the risks, choose to breast-feed. In these societies, HIV-infected women who deviate from the cultural norm of breast-feeding risk exposing their HIV status and becoming prey to negative social implications. For this group of women, defining strategies that can reduce their risk of transmitting HIV to their infants is essential. Based on data from previous studies, this study proposes to test the hypothesis that NVP will reduce breast-feeding transmission of HIV.

Pregnant HIV-positive women take an oral dose of NVP at the onset of labor. A second dose of NVP will be given 48 hours after the first dose if the woman remains in labor. Infants who initiate breast-feeding are randomized to 1 of the 3 study arms below and receive their first dose of NVP within 48 hours of birth.

Arm 1 receives NVP once a week, Arm 2 receives NVP twice a week, and Arm 3 receives NVP daily. There is no placebo control group. The first 18 infants enrolled in each arm will contribute pre- and post- NVP dose blood samples for pharmacokinetics. The remaining infants will contribute data on safety and pre-dose NVP levels only. Infants return to the clinic weekly for visual assessment of NVP toxicity. Women are counseled to stop breast-feeding their infants by the end of 6 months. Infants receive their last dose of NVP at either 24 weeks of age or 1 week after breast-feeding cessation, whichever occurs first, and have follow-up visits until the infant is 32 weeks old.

Interventional
Phase 1
Endpoint Classification: Safety Study
Primary Purpose: Prevention
HIV Infections
Drug: Nevirapine
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
75
May 2005
Not Provided

Inclusion Criteria

Mothers may be eligible for this study if they:

  • Receive prenatal care at King Edward VIII Hospital, Durban, or St. Mary's Hospital, Marianhill, South Africa; or polyclinics in Chitungwiza District, Zimbabwe.
  • Are pregnant for at least 30 weeks before giving birth.
  • Are at least 18 years of age.
  • Are HIV-positive by 2 ELISA tests.
  • Have no serious current or previous problems in pregnancy (e.g., seizures).
  • Have a fixed home and/or work address.
  • Plan to deliver the baby at a hospital or clinic where the study is based.
  • Plan to breast-feed their babies.
  • Infants may be eligible for this study if they:
  • Are born to women participating in this study.
  • Weigh at least 2.5 kg at birth.
  • Begin breast-feeding by 48 hours.

Exclusion Criteria

Mothers will not be eligible for this study if they:

  • Have AIDS or any other serious illness.
  • Are using illegal drugs or have been using alcohol for a long time.
  • Are sensitive to NVP.
  • Have taken any nonnucleoside reverse transcriptase inhibitors in the past.
  • Are using rifampin, rifabutin, ketoconazole, macrolides, or cimetidine.
  • Infants will not be eligible for this study if they:
  • Have jaundice (yellowing of the skin and whites of eyes) that requires a blood transfusion.
  • Have any serious or life-threatening condition(s).
Both
Not Provided
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00006279
HIVNET 023, 11720
Not Provided
National Institute of Allergy and Infectious Diseases (NIAID)
National Institute of Allergy and Infectious Diseases (NIAID)
Not Provided
Study Chair: Hoosen Coovadia
Study Chair: Mary Bassett
Study Chair: Salim Karim
National Institute of Allergy and Infectious Diseases (NIAID)
February 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP