LAC+USC MCA Clinic
Los Angeles, California, 90033, United States
NCT Number: NCT01625169
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.
Looking for future studies?
Notify Me18 year and older
Female
Interventional
Not applicable
Los Angeles, California, 90033, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
HIV+ pregnant women will receive etravirine 200mg PO BID for 14 days postpartum. PK will be done on postpartum days 5 and 14.
Time frame: Day 5
Cmax ng/ml
Note: One participant did not complete the Day 5 evaluation.
Time frame: day 5
Cmax ng/ml
Note: One participant did not complete the Day 5 evaluation.
Time frame: day 14
Cmax ng/mL
Time frame: day 14
Cmax ng/mL
Time frame: Day 5: 0, 2,4, 8 and 24 hours post dose
AUC 0-12 ng*hr/ml
Time frame: Day 14: 0, 2,4, 8 and 24 hours post dose
AUC 0-12 ng*hr/ml
Time frame: Day 5
AUC 0-12 ng*hr/ml
Time frame: Day 14
AUC 0-12 ng*hr/ml
Time frame: Day 5
Positive HIV RNA in breast milk and plasma- LDL 40 copies/ml
Time frame: Day 14
Positive HIV RNA in breast milk and plasma- LDL 40 copies/ml
University of Southern California
Other
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
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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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