HTB

Antiretrovirals

Small increase in birth defects in the French Perinatal Cohort

Uptake and retention in Malawi’s Option B+ programme

Optimising ART initiation in pregnancy through linkage of services vs integration of ART into antenatal care

EU approves four-in-one Stribild

FDA delays decision for elvitegravir and cobicistat

EU approval for raltegravir in children aged 2 years and older

FDA update label for paediatric efavirenz and capsule sprinkle formulation

Cobicistat compared to ritonavir to boost atazanavir in treatment naive patients

ARV pipeline: dolutegravir, TAF (GS-7340), MK-1439 and cenicriviroc

ARV pipeline: long-acting formulations of rilpivirine, GSK-744 and nanoformulations

Five-year results from the AntiRetroviral Research for Watoto (ARROW) Trial

Comparison of ritonavir-boosted lopinavir or NNRTI ART and PK with antimalarials in Ugandan children

Pharmacokinetics and acceptability of lopinavir/ritonavir sprinkles in children aged 1 to 4 years

Pharmacokinetics of currently available antiretroviral options for young children

Safety of transplacental raltegravir in neonates and washout pharmacokinetics

Tenofovir use in children

ddI resistance in South African children failing an abacavir or d4T based first-line regimen

Dietary requirements changed in Europe for fixed dose combination rilpivirine/tenofovir/FTC (Eviplera)

EU adopts positive opinion for decision on regulatory approval of Quad

Gilead Sciences announces fourth quarter and full year 2012 financial results

ViiV stops development of NNRTI lersivirine

Nelfinavir non-renewal of marketing authorisation in the EU

START study increases sample size: additional 600 participants to be older than 35

WHO statement: generic antiretroviral therapy is safe and effective

Nevirapine-containing ART does not reduce combined oral contraceptive effectiveness

Differences by age for women in response to initial ART: meta-analysis from clinical studies submitted to the FDA

Lopinavir/ritonavir in pregnancy: results from a systematic review

Dolutegravir submitted to EU, US and Canadian regulatory agencies

Darunavir: new oral suspension and 800 mg formulations approved in EU

US label changes for rilpivirine and Eviplera follows EU caution on high baseline viral load: new summary on drug resistance

Dolutegravir: integrase resistance and the impact of the background regimen

Updated results on Quad: 96 week data from phase 3 studies

Darunavir 800 mg tablet approved in the US

Study summaries from ICAAC 2012

Antiviral activity in vitro with S/GSK1265744

Efavirenz interaction studies with TB compounds bedaquiline and delamanid

HPTN-052: clinical advantages from earlier treatment

Online video interviews between researchers and activists

FDA approves Quad in US: price may prohibit UK access

Merck acquires CMX157 and EFdA and starts phase 2 study for new NNRTI

Roche to discontinue production of nelfinavir and saquinavir 200 mg hard capsules

New booster – cobicistat as an alternative to ritonavir

Dolutegravir vs raltegravir in treatment-naive patients: 48 week results from the SPRING 2 study

Elvitegravir vs raltegravir: 96 week phase III results in treatment experienced patients

In vitro and animal data support safety profile BMS 986001: d4T-like NRTI currently in clinical trials

Switching to rilpivirine/tenofovir/FTC fixed dose combination from boosted-PI regimen: SPIRIT study draws the line at 24 weeks

Maraviroc plus atazanavir/ritonavir in a nuke-sparing regimen in treatment-naive patients

Five-year results from raltegravir registrational studies

First report: atazanavir-related gallstones (cholelithiasis)

Novel lopinavir/ritonavir sprinkle formulation for children in resource-limited settings

Update on new antiretrovirals for children and adolescents

Efavirenz levels variable in children in the CHAPAS-3 study

Early initiation of ART is associated with growth recovery in children in NEVEREST-2

Lipid profile in children in PREDICT: immediate versus deferred nevirapine-based ART

Skeletal muscle toxicity and raltegravir

Dolutegravir indicates superiority compared to efavirenz in treatment-naïve patients: top-line results only

FDA update to darunavir label: severe skin reactions

Outcomes from switches to atazanavir/r in London

Studies on pipeline ARVs

Fosamprenavir paediatric dosing approved in US for ages 4 weeks to <6 years

FDA advisory panel vote 13:1 for approval of Quad

FDA advisory hearing supports approval of tenofovir/FTC for PrEP

Pharmacokinetics of atazanavir/ritonavir plus raltegravir

Renal impairment in the D:A:D study

Early data for rilpivirine long acting formulation supports further investigation for PrEP

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