Coverage of 2006 International
Conference on AIDS
August 14–18, 2006, Toronto, Canada
First Day Dominated by the
Two “Bills”—Clinton and Gates
by Paul Dalton, August 14, 2006
Day one at the 16th International AIDS Conference was dominated
by the two “Bills”—Clinton and Gates. Their joint
press conference commanded an overflow crowd, intent on hearing
news of their efforts to address the global pandemic. There was
plenty of star power and commitments of both funds and attention.
While it is always good to hear such things, it is results that
count. Can the ex-President and the World’s Richest Man make
a difference? Time will tell.
Things started out fairly light on the treatment research front.
The International Conference hasn’t been the scene of many
scientific breakthroughs since the famous Vancouver meeting, but
his year’s confab promises somewhat more for treatment activists
to chew on.
Press releases from two major players in the HIV pharmaceutical
front came out first thing in the morning highlighting their pipeline
and their products.
GlaxoSmithKline and Shionogi announced completion of the Phase
I safety study of their investigational integrase inhibitor, called
364735. No data were presented, but the companies did report the
results allowed them to choose a dose to move forward with for their
Phase II trial, set to open later this year. The companies also
announced they will present data from the Phase I trial at an ‘upcoming
medical conference in 2007’.
Gilead Sciences is presenting a range of studies of their products,
both approved and experimental. Gilead announced more data from
their pivotal 934 study comparing Atripla (Sustiva + Truvada) to
Sustiva + Combivir. The 96-week data were similar to the 48-week
data which were the basis for Atripla’s approval by the FDA.
More people taking Atripla had viral loads under 400 copies/ml (75%
vs. 62%) and better increases in CD4+ cell counts (270 vs. 237).
Also fewer people taking Atripla developed the M184V mutation associated
with resistance to both Epivir (lamivudine/3TC ... a component of
Combivir) and Emtriva (emtricitibine/FTC ... a component of Truvada).
Finally, there were fewer significant adverse events among those
taking Atripla, with anemia (6% vs. 0%) being the major difference.
Another Gilead poster looked at twelve different studies of Sustiva
plus various nucleoside backbones. Their poster showed Truvada performing
best compared to other backbone regimens, which included most of
the nucleosides currently in use. Finally, Gilead presented two
posters demonstrating a lack of drug-drug interactions between their
investigational II, GS-9137 (boosted with RTV) and Truvada and AZT.
There was an interesting oral abstract discussion on how HIV enters
immune system cells, which included new imaging technology allowing
scientists a better view of the HIV entry process, and more research
on HIV’s use of co-receptors CCR5 and CXCR4.
The first full day of the conference felt a bit disorganized and
scattered. On my plate for tomorrow are presentations on dendritic
cells, HIV replication dynamics, viral co-infections and hopefully
more.