Access to Hepatitis C Treatment in Cameroon: Comparison of a Simplified Test and Treat Strategy to a Standard Strategy

PHASE4Not yet recruitingINTERVENTIONAL
Enrollment

576

Participants

Timeline

Start Date

September 1, 2025

Primary Completion Date

December 31, 2027

Study Completion Date

June 30, 2028

Conditions
Hepatitis C Virus Infection
Interventions
DRUG

ACCESS+ strategy Epclusa 400/100 Oral Tablet

The ACCESS+ strategy will rely on four components: (1) same-day on-site rapid anti-HCV and HCV RNA testing (rapid diagnostic test and GeneXpert), (2) same-day on-site pan-genotypic DAA treatment initiation (sofosbuvir 400 mg/velpatasvir 100 mg once daily for 12 weeks), (3) minimal clinical and biological monitoring, and (4) management of patients in non-specialist services by trained general medical doctors and counselors (community health workers, nurses or social workers).

DRUG

ACCESS+ Strategy Vosevi 400/100/100 Oral Tablet

The ACCESS+ strategy will rely on four components: (1) same-day on-site rapid anti-HCV and HCV RNA testing (rapid diagnostic test and GeneXpert), (2) same-day on-site pan-genotypic DAA treatment initiation (sofosbuvir 400 mg/velpatasvir 100 mg/voxilaprevir 100mg) once daily for 12 weeks, (3) minimal clinical and biological monitoring, and (4) management of patients in non-specialist services by trained general medical doctors and counselors (community health workers, nurses or social workers).

DRUG

Standard Strategy Vosevi 400/100/100 Oral Tablet

In the standard strategy based on routine medical practice in Cameroon, anti-HCV positive participants will be referred to and managed by gastroenterologists who will initiate pan-genotypic DAA treatment initiation (sofosbuvir 400 mg/velpatasvir 100 mg/voxilaprevir 100mg) once daily for 12 weeks, and the patients' management will be closer. However, the process for screening and treatment initiation will be longer.

DRUG

Standard Strategy Epclusa 400/100 Oral Tablet

In the standard strategy based on routine medical practice in Cameroon, anti-HCV positive participants will be referred to and managed by gastroenterologists who will initiate pan-genotypic DAA treatment initiation (sofosbuvir 400 mg/velpatasvir 100 mg) once daily for 12 weeks, and the patients' management will be closer. However, the process for screening and treatment initiation will be longer.

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

IRD, Epidemiologie et Prevention, Montpelier, France

UNKNOWN

collaborator

SESSTIM (IRD, Inserm, Université Aix-Marseille)

UNKNOWN

collaborator

Centre de Recherche sur les Maladies Emergentes et Re-Emergentes (CREMER)

UNKNOWN

collaborator

Faculté de Médecine et des Sciences Biomédicales, Université de Yaoundé I, Yaoundé, Cameroun

UNKNOWN

collaborator

PharmAccess

UNKNOWN

collaborator

Service d'hépato-gastroentérologie, Hôpital Saint Joseph, Marseille, France

UNKNOWN

lead

ANRS, Emerging Infectious Diseases

OTHER_GOV