drugset / Trial / NCT01776996

An Expanded Access Protocol for Subjects Who Have Completed Clinical Studies Involving Maraviroc

NCT01776996 ↗

Expanded access No longer available ViiV Healthcare GlaxoSmithKline · collab

Summary

This is an open-label protocol designed to provide continued access to maraviroc to only those subjects who have completed previous studies of maraviroc and continue to receive clinical benefit.

Timeline

Start
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Primary completion
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Completion
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Drugs

EvaluationDrugModalityDoseRoute
Subject Maraviroc Other / unclassified 300 mg —
Background Lamivudine Other / unclassified 150 mg Oral
Background Zidovudine Small molecule 300 mg Oral