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Atazanavir pharmacokinetics with and without tenofovir during pregnancy.
- Source :
-
Journal of acquired immune deficiency syndromes (1999) [J Acquir Immune Defic Syndr] 2011 Apr 15; Vol. 56 (5), pp. 412-9. - Publication Year :
- 2011
-
Abstract
- Background: Few data are available describing atazanavir exposure during pregnancy, especially when used in combination with tenofovir, whose coadministration with atazanavir results in decreased atazanavir exposure.<br />Design: International Maternal Pediatric Adolescent AIDS Clinical Trials 1026 s is an ongoing, prospective, nonblinded study of antiretroviral pharmacokinetics in HIV-infected pregnant women that included 2 cohorts receiving atazanavir/ritonavir 300 mg/100 mg once daily, either with or without tenofovir.<br />Methods: Intensive steady-state 24-hour pharmacokinetic profiles were performed during the third trimester and at 6-12 weeks postpartum. Atazanavir was measured by reverse-phase high-performance liquid chromatography (detection limit 0.047 mcg/mL). Pharmacokinetic targets were the estimated 10th percentile atazanavir area under the concentration versus time curve [(AUC): 29.4 mcg · hr · mL-1] in nonpregnant historical controls (mean AUC = 57 mcg · hr · mL-1) and a trough concentration of 0.15 mcg/mL, the concentration target used in therapeutic drug monitoring programs.<br />Results: Median atazanavir AUC was reduced during the third trimester compared with postpartum for subjects not receiving tenofovir (41.9 vs. 57.9 mcg · hr · mL-1, P = 0.02) and for subjects receiving tenofovir (28.8 vs. 39.6 mcg · hr · mL-1, P = 0.04). During the third trimester, AUC was below the target in 33% (6 of 18) of women not receiving tenofovir and 55% (11 of 20) of women receiving tenofovir. Trough concentration was below the target in 6% (1 of 18) of women not receiving tenofovir and 15% (3 of 20) of women receiving tenofovir. The median (range) ratio of cord blood/maternal atazanavir concentration in 29-paired samples was 0.18 (0-0.45).<br />Conclusions: Atazanavir exposure is reduced by pregnancy and by concomitant tenofovir use. A dose increase of atazanavir/ritonavir to 400 mg/100 mg may be necessary in pregnant women to ensure atazanavir exposure equivalent to that seen in nonpregnant adults.
- Subjects :
- Adenine administration & dosage
Adenine pharmacokinetics
Anti-HIV Agents administration & dosage
Atazanavir Sulfate
Drug Administration Schedule
Drug Monitoring
Drug Therapy, Combination
Female
HIV Infections prevention & control
HIV Infections transmission
HIV Infections virology
HIV Protease Inhibitors administration & dosage
HIV Protease Inhibitors pharmacokinetics
HIV-1 drug effects
Humans
Infectious Disease Transmission, Vertical prevention & control
Oligopeptides administration & dosage
Organophosphonates administration & dosage
Postpartum Period
Pregnancy
Pregnancy Complications, Infectious virology
Pregnancy Trimester, Third
Prospective Studies
Pyridines administration & dosage
Reverse Transcriptase Inhibitors administration & dosage
Ritonavir administration & dosage
Ritonavir pharmacokinetics
Tenofovir
Treatment Outcome
Adenine analogs & derivatives
Anti-HIV Agents pharmacokinetics
HIV Infections drug therapy
Oligopeptides pharmacokinetics
Organophosphonates pharmacokinetics
Pregnancy Complications, Infectious drug therapy
Pyridines pharmacokinetics
Reverse Transcriptase Inhibitors pharmacokinetics
Subjects
Details
- Language :
- English
- ISSN :
- 1944-7884
- Volume :
- 56
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Journal of acquired immune deficiency syndromes (1999)
- Publication Type :
- Academic Journal
- Accession number :
- 21283017
- Full Text :
- https://doi.org/10.1097/QAI.0b013e31820fd093