HIV Infections Clinical Trial
Official title:
A Phase 2, Open-Label, Multicenter Study of the Safety of Ritonavir-Boosted GS-9137 (GS-9137/r) Administered in Combination With Other Antiretroviral Agents for the Treatment of HIV-1 Infected Subjects
This study is being initiated to provide continued access to ritonavir-boosted elvitegravir
(EVG/r; GS-9137/r) for those participants currently benefiting from their participation in
an ongoing EVG/r study. This study will also provide initial access to EVG/r for those
participants who have completed a EVG/r study in which the participant was participating in
a treatment arm that did not include EVG/r.
While on study, participants will be monitored for safety using periodic assessments of
concomitant medications, adverse events and laboratory tests. Participants will be seen once
every 8 weeks for the first 48 weeks of the study. Upon completion of 48 weeks, study visits
will occur once every 12 weeks until EVG becomes commercially available, or until Gilead
elects to terminate the study.
n/a
Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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