Phase 2a EBA Trial of AZD5847

PHASE2CompletedINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

December 5, 2012

Primary Completion Date

December 12, 2013

Study Completion Date

December 24, 2013

Conditions
Tuberculosis
Interventions
DRUG

AZD5847

Eligible subjects will be randomly assigned to receive monotherapy with one of four doses of oral AZD5847 for 14 days: 500 mg orally once daily, 500 mg orally twice daily, 1200 mg orally once daily, or 800 mg orally twice daily.

DRUG

Ethambutol, isoniazid, pyrazinamide, rifampin

Eligible subjects will be randomly assigned to receive treatment with standard 4 drug anti-tuberculosis regimen: Rifafour e-275 mg tablets (75 mg isoniazid/150 mg Rifampin/275 mg Ethambutol/400 mg Pyrazinamide) orally, dosed by body weight for 14 days.

Trial Locations (1)

7530

Task Clinical Research Centre, Ekurhuleni

All Listed Sponsors
lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

NCT01516203 - Phase 2a EBA Trial of AZD5847 | Biotech Hunter | Biotech Hunter