BackgroundRapid reduction in human immunodeficiency virus (HIV) load is paramount to prevent peripartum transmission in women diagnosed late in pregnancy. We investigated dolutegravir population pharmacokinetics in maternal plasma, umbilical cord, breast milk, and infant plasma samples from DolPHIN-1 participants (NCT02245022) presenting with untreated HIV late in pregnancy (28-36 weeks gestation).MethodsPregnant women from Uganda and South Africa were randomized (1:1) to daily dolutegravir (50 mg/d) or efavirenz-based therapy. Dolutegravir pharmacokinetic sampling (0-24 hours) was undertaken 14 days after treatment initiation and within 1-3 weeks after delivery, with matched maternal and cord samples at delivery. Mothers were switched to e...
BackgroundMaternal-to-fetal transfer of antiretroviral drugs contributes to prevention of vertical t...
In 2018, Switzerland changed its guidelines to support women living with HIV wishing to breastfeed. ...
An intensive, prospective, open-label pharmacokinetic (PK) study in a subset of HIV-infected mothers...
BackgroundThe global transition to use of dolutegravir (DTG) in WHO-preferred regimens for HIV treat...
ObjectiveTo evaluate dolutegravir pharmacokinetics during pregnancy compared with postpartum and in ...
Background: ART initiation in the 3rd trimester of pregnancy is associated with failure to achieve v...
BACKGROUND: Pharmacokinetic and efficacy data on dolutegravir in pregnant women living with human im...
BACKGROUND:Remarkable progress has been achieved in the identification of HIV infection in pregnant ...
OBJECTIVES: Data on fetal exposure to antiretroviral agents during pregnancy are important to estima...
BACKGROUND: Late initiation of HIV antiretroviral therapy (ART) in pregnancy is associated with not ...
BackgroundLate initiation of antiretrovirals in pregnancy is associated with increased risk of perin...
BACKGROUND: Limited data exist on efavirenz pharmacokinetics in HIV-positive pregnant women and neon...
DolPHIN-1 is an RCT of dolutegravir versus efavirenz in women initiating treatment in the third trim...
BackgroundA knowledge gap exists for dolutegravir (DTG) pharmacokinetics and safety during the first...
International audienceOBJECTIVE:To determine the transplacental pharmacokinetics of the HIV integras...
BackgroundMaternal-to-fetal transfer of antiretroviral drugs contributes to prevention of vertical t...
In 2018, Switzerland changed its guidelines to support women living with HIV wishing to breastfeed. ...
An intensive, prospective, open-label pharmacokinetic (PK) study in a subset of HIV-infected mothers...
BackgroundThe global transition to use of dolutegravir (DTG) in WHO-preferred regimens for HIV treat...
ObjectiveTo evaluate dolutegravir pharmacokinetics during pregnancy compared with postpartum and in ...
Background: ART initiation in the 3rd trimester of pregnancy is associated with failure to achieve v...
BACKGROUND: Pharmacokinetic and efficacy data on dolutegravir in pregnant women living with human im...
BACKGROUND:Remarkable progress has been achieved in the identification of HIV infection in pregnant ...
OBJECTIVES: Data on fetal exposure to antiretroviral agents during pregnancy are important to estima...
BACKGROUND: Late initiation of HIV antiretroviral therapy (ART) in pregnancy is associated with not ...
BackgroundLate initiation of antiretrovirals in pregnancy is associated with increased risk of perin...
BACKGROUND: Limited data exist on efavirenz pharmacokinetics in HIV-positive pregnant women and neon...
DolPHIN-1 is an RCT of dolutegravir versus efavirenz in women initiating treatment in the third trim...
BackgroundA knowledge gap exists for dolutegravir (DTG) pharmacokinetics and safety during the first...
International audienceOBJECTIVE:To determine the transplacental pharmacokinetics of the HIV integras...
BackgroundMaternal-to-fetal transfer of antiretroviral drugs contributes to prevention of vertical t...
In 2018, Switzerland changed its guidelines to support women living with HIV wishing to breastfeed. ...
An intensive, prospective, open-label pharmacokinetic (PK) study in a subset of HIV-infected mothers...