<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Luque AE</submitter><funding>NCATS NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIAID NIH HHS</funding><pagination>2094-101</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4356823</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>59(4)</volume><pubmed_abstract>We conducted an open-label, steady-state pharmacokinetic (PK) study of drug-drug interactions between depot medroxyprogesterone acetate (DMPA) and twice-daily lopinavir (LPV) plus low-dose ritonavir (RTV) (LPV/r) among 24 HIV-infected women and compared the results to those for HIV-infected women receiving DMPA while on no antiretroviral therapy or on nucleosides only (n = 14 subjects from the control arm of AIDS Clinical Trials Group [ACTG] study 5093). The objectives of the study were to address the effect of LPV/r on DMPA and to address the effect of DMPA on LPV/r therapy. PK parameters were estimated using noncompartmental analysis with between-group comparisons of medroxyprogesterone acetate (MPA) PKs and within-subject comparisons of LPV and RTV PKs before and 4 weeks after DMPA dosi</pubmed_abstract><journal>Antimicrobial agents and chemotherapy</journal><pubmed_title>Depot medroxyprogesterone acetate in combination with a twice-daily lopinavir-ritonavir-based regimen in HIV-infected women showed effective contraception and a lack of clinically significant interactions, with good safety and tolerability: results of the ACTG 5283 study.</pubmed_title><pmcid>PMC4356823</pmcid><funding_grant_id>UM1 AI069423</funding_grant_id><funding_grant_id>P30 AI050410</funding_grant_id><funding_grant_id>AI068634</funding_grant_id><funding_grant_id>UL1 TR000150</funding_grant_id><funding_grant_id>UM1 AI068632</funding_grant_id><funding_grant_id>UM1AI068616</funding_grant_id><funding_grant_id>UM1 AI106716</funding_grant_id><funding_grant_id>U01 AI069481</funding_grant_id><funding_grant_id>UM1 AI068634</funding_grant_id><funding_grant_id>UM1AI068636</funding_grant_id><funding_grant_id>UM1 AI068636</funding_grant_id><funding_grant_id>UM1AI106716</funding_grant_id><funding_grant_id>1U01AI068636</funding_grant_id><funding_grant_id>UM1 AI068616</funding_grant_id><funding_grant_id>UM1AI068632</funding_grant_id><funding_grant_id>UL1TR000150</funding_grant_id><funding_grant_id>U01 AI068636</funding_grant_id><funding_grant_id>UL-1RR02460</funding_grant_id><funding_grant_id>UM1 AI069481</funding_grant_id><funding_grant_id>1U01AI069481</funding_grant_id><funding_grant_id>UM1 AI106701</funding_grant_id><funding_grant_id>UM1 AI069511</funding_grant_id><funding_grant_id>P30 AI50410</funding_grant_id><funding_grant_id>U01 AI069471</funding_grant_id><funding_grant_id>UL1 TR002489</funding_grant_id><funding_grant_id>P30 AI027763</funding_grant_id><funding_grant_id>UL1 TR001111</funding_grant_id><funding_grant_id>1U01AI069513</funding_grant_id><funding_grant_id>1U01AI069511</funding_grant_id><funding_grant_id>1U01AI069471</funding_grant_id><funding_grant_id>1UL1TR001111</funding_grant_id><funding_grant_id>UM1 AI069471</funding_grant_id><funding_grant_id>UM1-AI069423-08</funding_grant_id><funding_grant_id>UM1 AI069496</funding_grant_id><funding_grant_id>U01 AI069511</funding_grant_id><funding_grant_id>U01 AI069513</funding_grant_id><pubmed_authors>Weinberg A</pubmed_authors><pubmed_authors>Klingman KL</pubmed_authors><pubmed_authors>Park JG</pubmed_authors><pubmed_authors>Livingston E</pubmed_authors><pubmed_authors>Cohn SE</pubmed_authors><pubmed_authors>Watts DH</pubmed_authors><pubmed_authors>Luque AE</pubmed_authors><pubmed_authors>Cramer Y</pubmed_authors><pubmed_authors>Aweeka F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Depot medroxyprogesterone acetate in combination with a twice-daily lopinavir-ritonavir-based regimen in HIV-infected women showed effective contraception and a lack of clinically significant interactions, with good safety and tolerability: results of the ACTG 5283 study.</name><description>We conducted an open-label, steady-state pharmacokinetic (PK) study of drug-drug interactions between depot medroxyprogesterone acetate (DMPA) and twice-daily lopinavir (LPV) plus low-dose ritonavir (RTV) (LPV/r) among 24 HIV-infected women and compared the results to those for HIV-infected women receiving DMPA while on no antiretroviral therapy or on nucleosides only (n = 14 subjects from the control arm of AIDS Clinical Trials Group [ACTG] study 5093). The objectives of the study were to address the effect of LPV/r on DMPA and to address the effect of DMPA on LPV/r therapy. PK parameters were estimated using noncompartmental analysis with between-group comparisons of medroxyprogesterone acetate (MPA) PKs and within-subject comparisons of LPV and RTV PKs before and 4 weeks after DMPA dosi</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Apr</publication><modification>2025-04-04T19:19:57.216Z</modification><creation>2019-03-27T01:48:02Z</creation></dates><accession>S-EPMC4356823</accession><cross_references><pubmed>25624326</pubmed><doi>10.1128/AAC.04701-14</doi><doi>10.1128/aac.04701-14</doi></cross_references></HashMap>