Feasibility of Intravaginal Artesunate as Adjuvant HPV & Cervical Precancer Treatment in Kenya

PHASE2RecruitingINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

January 22, 2025

Primary Completion Date

November 30, 2025

Study Completion Date

November 30, 2025

Conditions
Human Immunodeficiency VirusHuman PapillomavirusCervical Precancer
Interventions
DRUG

Artesunate vaginal inserts

Subjects will self-administer 200 mg of Artesunate vaginal insert daily for 5 days, on weeks 1, 3, 5.

DRUG

Placebo vaginal inserts

Subjects will self-administer a placebo vaginal insert daily for 5 days, on weeks 1, 3, 5.

Trial Locations (1)

614-40100

RECRUITING

Lumumba Sub-County Hospital KEMRI- Research Care Training Program (RCTP) Building, Kisumu

Sponsors
All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

collaborator

Kenya Medical Research Institute

OTHER

collaborator

Maseno University School of Medicine, Kenya

UNKNOWN

lead

UNC Lineberger Comprehensive Cancer Center

OTHER