ANRS 12372 MODERATO Study

PHASE3UnknownINTERVENTIONAL
Enrollment

480

Participants

Timeline

Start Date

September 21, 2020

Primary Completion Date

February 5, 2025

Study Completion Date

February 5, 2025

Conditions
HIV-1-infection
Interventions
DRUG

dolutegravir

One daily tablet (50mg) during 96 weeks

DRUG

atazanavir boosted with ritonavir

One daily tablet with atazanavir (300 mg) boosted with ritonavir (100 mg) during 96 weeks

DRUG

tenofovir + lamivudine +efavirenz or dolutegravir + lamivudine + tenofovir

One daily tablet with tenofovir 245 mg + lamivudine (300 mg) + efavirenz (400 mg) during 96 weeks OR One daily tablet with dolutegravir 50 mg + lamivudine (300 mg) + tenofovir (300 mg) during 96 weeks

DRUG

Lamivudine

One daily tablet (300mg) during 96 weeks

Trial Locations (5)

Unknown

Hôpital de jour, Service des maladies infectieuses, CHU Sourô Sanou, Bobo-Dioulasso

Service de médecine interne, CHU Yalgado Ouédraogo, Ouagadougou

Service des Maladies Infectieuses, Hôpital du jour, Hôpital Central, Yaoundé

Centre de Prise en Charge et de Formation (CePReF), Association ACONDA, Abidjan

Service des Maladies Infectieuses et Tropicales (SMIT), CHU de Treichville, Abidjan

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Mylan Laboratories

INDUSTRY

lead

ANRS, Emerging Infectious Diseases

OTHER_GOV

NCT04022967 - ANRS 12372 MODERATO Study | Biotech Hunter | Biotech Hunter