A Phase 2 Trial to Evaluate the EBA, Safety and Tolerability of Eto Alone and in Combination With BVL-GSK098

PHASE2CompletedINTERVENTIONAL
Enrollment

105

Participants

Timeline

Start Date

December 6, 2022

Primary Completion Date

April 16, 2024

Study Completion Date

April 16, 2024

Conditions
Rifampicin- and Isoniazid-Susceptible Pulmonary Tuberculosis (TB)
Interventions
DRUG

BVL-GSK098 9mg

BVL-GSK098 9 mg once daily po OD plus ethionamide 250 mg po OD (b9Eto250) BVL-GSK098 27 mg OD plus ethionamide 125 mg po OD (b27Eto125 BVL-GSK098 27 mg OD plus ethionamide 250 mg po OD (b27Eto250) BVL-GSK098 27 mg OD plus ethionamide 500 mg po OD (b27Eto500)

DRUG

Ethionamide 250mg

Ethionamide 250 mg po OD (Eto250)

DRUG

Ethionamide 250 mg

Ethionamide 750 mg po given in a single or divided dose (Eto750)

DRUG

Isoniazid 300 MG

Isoniazid 300 mg po OD (INH)

Trial Locations (1)

7530

TASK Clinical Research Centre, Cape Town

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

TASK Applied Science

OTHER