Antiretrovirals

Atazanavir launched in UK

Tenofovir/FTC co-formulation application made to EMEA

Abacavir/3TC co-formulation available in expanded access

Treatment with generics: tolerability, safety and resistance

Drug levels can persist for more than two weeks after stopping efavirenz

COLATE study shows no clinical benefit from continuing 3TC to maintain M184V mutation

Studies of new pipeline drugs

Little benefit seen for treatment during acute infection

Gilead discontinues DAPD development

Abbott raises price of ritonavir in the US by over 400%

Development of T-1249 put on hold

Tenofovir/abacavir/3TC triple-nuke fails as maintenance regimen

New data on viral load ‘blips’ and the link to replication

Invirase and Fortovase: new dosing regimens approved by FDA

UK named-patient access to tipranavir

FDA labelling changes for indinavir (Crixivan)

Switching from efavirenz to nevirapine to avoid CNS side effects

T20 is cost effective for UK purchasers

African patients and adherence in the UK

Five-year results of Kaletra-based therapy in treatment-naïve HIV patients

Rituximab plus CDE for HIV-related Non-Hodgkins Lymphoma (NHL)

FTC (emtricitabine, Emtriva) approved in Europe

EMEA recommend approval for atazanavir for treatment experienced patients

Fosamprenavir (Lexiva) approved in US

US paediatric, adult and maternal-child guidelines updated

ddI may retain activity in nucleoside experienced patients

Studies and strategies with existing drugs

Incremental progress with new antiviral drugs

Atazanavir ‘named-patient’ access extended in the UK and includes 150mg capsule

Another triple nuke failure: abacavir/ddI/d4T

FDA announces changes to ritonavir package insert

New atazanavir information

Boosted PI therapy antiretrovirals in treatment-experienced patients: SQV/r, ATV, ATV/r

Tenofovir, resistance and K65R and concomitant nucleosides

Mitochondrial toxicity with AZT and d4T – and benefits of switch to abacavir

Nevirapine and MTCT: the single-dose backlash

Triple nucleoside combinations fail patients again

Nucleoside-sparing regimens

Dual boosted PIs in salvage therapy

BMS reports on atazanavir efficacy and safety in treatment experienced patients

Unsupervised treatment interruptions are associated with increased risk of AIDS or death

Step-wise intervention eases diarrhoea linked to PI nelfinavir (Viracept) therapy

Lessons learned from early HAART in acute HIV infection

CD4 cell reconstitution is significantly slower in older patients

Pharmacology studies at the 2nd IAS conference

T-20 launched in UK

US approval of FTC (emtricitabine)

T-20 approved in Europe

Tenofovir European licence extended to include first-line therapy

FDA approves atazanavir in US – a once daily protease inhibitor

Atanazavir and saquinavir in salvage therapy: reduced effect on lipids shown in pilot study

Major change to OPTIMA salvage therapy study in the UK

New 625mg formulations of nelfinavir

Lopinavir suitable for TDM

Less diarrhoea and bioequivalence with the new nelfinavir 625mg tablet

T-20 access programme to continue in UK for a further two months

Durability and success capability of HAART: 4.5 years follow-up

Older HIV-positive patients in the era of HAART: changing of a scenario

Immune reconstitution in older HIV-positive individuals

Pipeline compounds in Phase 2/3 Studies

96-week results show tenofovir-including regimen has side-effect advantages over d4T regimen in treatment naïve patients

2NN results – nevirapine and efavirenz in prospective randomised head-to-head study

NIH/NIAID study of generic drugs shows results consistent with stringent manufacturing standards

Treatment interruptions: cycles, pauses, are just plain stopping?

Trizivir-only arm closed in PI-sparing, naïve therapy trial

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