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OpenTrials
Completed

NCT Number: NCT01625169

Etravirine Pharmacokinetics and HIV Viral Load in Breast Milk and Plasma

HIV positive pregnant women who receive potent combination antiretroviral therapy over at least the last trimester of pregnancy, and who have proper obstetric interventions and are able to avoid breast feeding, decrease the risk of having an infected infant to about 1%. Breast milk HIV-1 RNA (cell free) viral load is significantly associated with breast milk transmission, and a 2-fold increased risk of transmission associated with every 10-fold increase in breast milk viral load has been reported. In addition, cell associated virus (HIV DNA) was associated with a significant increase in risk of transmission independent of the level of cell-free viral RNA.

However, multiple studies of HIV positive women giving birth have shown that exclusive breast-feeding carries a much lower risk of HIV transmission than mixed breast-feeding (defined as breast milk along with complementary food, other milk, and/or infant formula). The proposed study will measure the antiretroviral (ARV) drug etravirine concentrations in blood and breast milk in postpartum HIV positive women on HAART therapy. The short-term goal is to determine how much etravirine penetrates into breast milk, and whether it leads to undetectable HIV viral load in the breast milk and therefore has the potential to decrease the risk of transmission of HIV through breast milk. The long term goal is to see if breast milk HIV levels can be lowered sufficiently to prevent maternal to child transmission (MTCT) of HIV in infants receiving only breast feeding in resource poor areas.

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Key information

Conditions

HIV

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

LAC+USC MCA Clinic

Los Angeles, California, 90033, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV+ pregnant women on HAART for the prevention of MTCT w/ undetectable viral load at time of delivery (w/i 30 days of delivery).
  • 18 years and older
  • Only women who are deemed by the physician as being capable of understanding that HIV positive women should not breastfeed will be approached.
  • Life expectancy greater than 6 months
  • No known allergies to etravirine
  • Willingness of subject to adhere to protocol requirements.

Exclusion criteria

  • Pregnant women with medical or psychological contraindications to breast milk expression.
  • Requirements for prohibited medications:
  • ARV: Tipranavir/ritonavir, fosamprenavir/ritonavir, atazanavir/ritonavir, and protease inhibitors administered without ritonavir, nonnucleoside reverse transcriptase inhibitor (NNRTIs).
  • Alternative/CAM: St. John's wort
  • Anticonvulsants: Phenobarbital, carbamazepine , phenytoin
  • Anti-infectives: Rifampin

Treatment and study plan

Etravirine pharmacokinetics in breast milk and plasma

Drug

HIV+ pregnant women will receive etravirine 200mg PO BID for 14 days postpartum. PK will be done on postpartum days 5 and 14.

Primary outcomes

  1. Peak Plasma Concentration of Etravirine in Plasma

    Time frame: Day 5

    Cmax ng/ml

    Note: One participant did not complete the Day 5 evaluation.

  2. Peak Concentration of Etravirine in Breast Milk

    Time frame: day 5

    Cmax ng/ml

    Note: One participant did not complete the Day 5 evaluation.

  3. Peak Concentration of Etravirine in Breast Milk

    Time frame: day 14

    Cmax ng/mL

  4. Peak Plasma Concentration of Etravirine in Plasma

    Time frame: day 14

    Cmax ng/mL

  5. Area Under the Curve (AUC) 0-12 for Plasma

    Time frame: Day 5: 0, 2,4, 8 and 24 hours post dose

    AUC 0-12 ng*hr/ml

  6. Area Under the Curve (AUC) 0-12 for Plasma

    Time frame: Day 14: 0, 2,4, 8 and 24 hours post dose

    AUC 0-12 ng*hr/ml

  7. Area Under the Curve (AUC) 0-12 for Breast Milk

    Time frame: Day 5

    AUC 0-12 ng*hr/ml

  8. Area Under the Curve (AUC) 0-12 for Breast Milk

    Time frame: Day 14

    AUC 0-12 ng*hr/ml

Secondary outcomes

  1. HIV Viral Load in Breast Milk and Plasma

    Time frame: Day 5

    Positive HIV RNA in breast milk and plasma- LDL 40 copies/ml

  2. HIV Viral Load in Breast Milk and Plasma

    Time frame: Day 14

    Positive HIV RNA in breast milk and plasma- LDL 40 copies/ml

Sponsors and collaborators

Lead sponsor

University of Southern California

Other

Collaborators

  • Tibotec Therapeutics, a Division of Ortho Biotech Products, L.P., USA

Registry information

Official study title

Antiretroviral Drug Concentrations and HIV Viral Load in Breast Milk and Plasma in HIV+ Women Receiving HAART (Highly Active Antiretroviral Therapy) Therapy: Etravirine (ETR) Pharmacokinetics (PK) in Breast Milk and Plasma

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Jun 21, 2012
Registry last updated
Aug 13, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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