Etravirine Pharmacokinetics and HIV Viral Load in Breast Milk and Plasma
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
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.
調査の概要
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
-
-
California
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Los Angeles、California、アメリカ、90033
- LAC+USC MCA Clinic
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-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
他の:HIV + pregnant women
Etravirine pharmacokinetics in breast milk and plasma.
Etravirine 200mg PO BID for 14 days with PK on days 5 and 14
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HIV+ pregnant women will receive etravirine 200mg PO BID for 14 days postpartum.
PK will be done on postpartum days 5 and 14.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Peak Plasma Concentration of Etravirine in Plasma
時間枠:Day 5
|
Cmax ng/ml Note: One participant did not complete the Day 5 evaluation. |
Day 5
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Peak Concentration of Etravirine in Breast Milk
時間枠:day 5
|
Cmax ng/ml Note: One participant did not complete the Day 5 evaluation. |
day 5
|
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Peak Concentration of Etravirine in Breast Milk
時間枠:day 14
|
Cmax ng/mL
|
day 14
|
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Peak Plasma Concentration of Etravirine in Plasma
時間枠:day 14
|
Cmax ng/mL
|
day 14
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Area Under the Curve (AUC) 0-12 for Plasma
時間枠:Day 5: 0, 2,4, 8 and 24 hours post dose
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AUC 0-12 ng*hr/ml
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Day 5: 0, 2,4, 8 and 24 hours post dose
|
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Area Under the Curve (AUC) 0-12 for Plasma
時間枠:Day 14: 0, 2,4, 8 and 24 hours post dose
|
AUC 0-12 ng*hr/ml
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Day 14: 0, 2,4, 8 and 24 hours post dose
|
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Area Under the Curve (AUC) 0-12 for Breast Milk
時間枠:Day 5
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AUC 0-12 ng*hr/ml
|
Day 5
|
|
Area Under the Curve (AUC) 0-12 for Breast Milk
時間枠:Day 14
|
AUC 0-12 ng*hr/ml
|
Day 14
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
HIV Viral Load in Breast Milk and Plasma
時間枠:Day 5
|
Positive HIV RNA in breast milk and plasma- LDL 40 copies/ml
|
Day 5
|
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HIV Viral Load in Breast Milk and Plasma
時間枠:Day 14
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Positive HIV RNA in breast milk and plasma- LDL 40 copies/ml
|
Day 14
|
協力者と研究者
捜査官
- 主任研究者:LaShonda Y Spencer, MD、University of Southern California
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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