GSK's majority-owned ViiV Healthcare unit said on Wednesday the
experimental two-drug injection of cabotegravir and rilpivirine
maintained similar rates of viral suppression compared with a
standard three-drug oral regimen, after 48 weeks of a clinical
trial.
The result from the big Phase III study is a boost for GSK's goal of
developing dual therapies that are easier to tolerate than
conventional triple ones, and shares in GSK rose more than 1
percent. It follows recent positive data from combining two oral
drugs.
GSK hopes its new approach will allow it to compete more effectively
against Gilead Sciences, the U.S. drugmaker that dominates the $26
billion-a-year HIV market.
Gilead currently has a market share of around 52 percent against
GSK's 22 percent, but Deborah Waterhouse, who heads the British
drugmaker's HIV unit, says she hopes to overtake her U.S. rival by
the mid-2020s.
That is a bold ambition, since many analysts have been expecting GSK
to lose market share to Gilead's new triple drug Biktarvy, rather
than see it gain ground.
Liberum analyst Roger Franklin, who rates GSK a 'buy', believes the
company's dual-drug strategy has been under-appreciated by the
market.
"Whilst duals will likely be a slow burn as resistance data is
collected and the regimen gains credence among physicians, the
prospects are much improved now versus a year ago," he said.
GSK is betting that a shift to using two drugs rather than three
will boost its sales by offering patients a therapy with greater
convenience and fewer toxic side effects. In certain cases,
depending on the drugs used, two-drug regimens will also be
significantly cheaper.
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Still, some doctors worry that using just two drugs to keep the AIDS
virus at bay might risk drug resistance because HIV will only have
to evade two drugs rather than three. That is certainly the view at
Gilead, which is sticking with three.
In the case of the cabotegravir and rilpivirine monthly injection,
GSK said drug resistance results in the latest study were consistent
with data from earlier smaller trials. It did not go into further
details but said full results would be presented at an upcoming
scientific meeting.
ViiV Chief Scientific and Medical Officer John Pottage argued the
novel injection offered an alternative long-term treatment for
patients.
"If approved, this regimen would give people living with HIV one
month between each dose of antiretroviral therapy, changing HIV
treatment from 365 dosing days per year, to just 12," he said.
Results from a second trial of cabotegravir and rilpivirine are
expected later this year. Rilpivirine was developed by Johnson &
Johnson and GSK is working with the U.S. drugmaker on the new
injection regimen.
(Reporting by Ben Hirschler; editing by David Evans and Emelia
Sithole-Matarise)
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