Combivir And Maraviroc In Antiretroviral Naive Subjects In Russia

PHASE4CompletedINTERVENTIONAL
Enrollment

98

Participants

Timeline

Start Date

June 30, 2011

Primary Completion Date

October 31, 2012

Study Completion Date

July 31, 2013

Conditions
HIV
Interventions
DRUG

HIV therapy

Combivir one tablet BD with maraviroc 300mg BD for 48 weeks

Trial Locations (8)

105275

Federal scientific and methodological center on AIDS prophylaxis and control, Moscow

129110

Moscow regional center on AIDS and infectious diseases prophylaxis and control, Moscow

190103

Saint-Petersburg Center on AIDS and Infectious Diseases Prophylaxis and Control, Saint Petersburg

196645

Federal State Institution Republican clinical infectious hospital of Roszdrav, Saint Petersburg

214006

Smolensk Center on AIDS and infectious diseases prophylaxis and control, Smolensk

400040

Volgograd Regional Center on AIDS and Infectious Diseases Prophylaxis and Control, Volgograd

603005

Regional Center on AIDS and Infectious Diseases Prophylaxis and Control, Nizhny Novgorod

660049

Regional Center on AIDS and Infectious Diseases Prophylaxis and Control, Krasnoyarsk

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Pfizer

INDUSTRY

lead

ViiV Healthcare

INDUSTRY

NCT01275625 - Combivir And Maraviroc In Antiretroviral Naive Subjects In Russia | Biotech Hunter | Biotech Hunter