Search Menu

Antiretrovirals

Importance of intensive adherence support for people with HIV-related neurological symptoms

Efavirenz side effects become long-term for over one in three

ABT-378/r oral formulation available in UK

Trimeris, Roche to begin phase III pivotal trials of T-20 HIV fusion inhibitor

United States FDA approves Kaletra for HIV infection

Videx EC (ddI, didanosine) – food restrictions

Importance of protease inhibitor plasma levels in patients treated with genotypic-guided therapy

Flavopiridol inhibits cellular processes essential to replication of HIV

Abbott expands early-access program for ABT-378/r (Kaletra)

Roche and Trimeris announce intention to manufacture commercial supplies of anti-HIV fusion inhibitor T-20

PRO-542 shows efficacy in trial

New potential dual NNRTI-based combinations

Once-daily protease-based regimens

European drug approvals: amprenavir, ddI EC, Trizivr and Kaletra

DAPD shows activity in vitro against multidrug-resistant HIV but initial results from monotherapy in treatment experienced subjects are disappointing

Indinavir/ritonavir at 400/400 mg or 800/100 mg as intensification

Ritonavir/saquinavir combination: effect of ritonavir dosage

Nevirapine vs efavirenz: the SENC trial

Nevirapine daily exposure for daily 400 mg dose compared to 200 mg twice-daily

Didanosine systemic exposure in children similar with or without food, high interpatient variability suggests TDM to titrate individual dosages

Low level HIV replication despite good virological response may explain CD4+ cell decline in a patient receiving combination nucleoside analogue therapy

ABT-378/r (lopinavir) now available on named patient basis in UK

Enteric coated ddI available on named patient basis in UK

Nelfinavir potency concerns

Post navigation