Efficacy of HUEXC030 in Subjects With Pulmonary Tuberculosis

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

557

Participants

Timeline

Start Date

December 6, 2012

Primary Completion Date

January 9, 2019

Study Completion Date

January 9, 2019

Conditions
Pulmonary Tuberculosis
Interventions
DRUG

Isoniazid with HUEXC030 and RZE

Subjects will receive oral study drug daily in accordance with the following regimen, that is, INH, RMP, PZA, and EMB for the first 2 months followed by INH, RMP and EMB (if medically indicated) daily for 4 additional months

DRUG

HRZE

the same as experimental group,without the excipient of HUEXC030 only

Trial Locations (18)

112

Taipei Veterans General Hospital, Taipei

11490

Tri-Service General Hospital, Taipei

Unknown

Changhua Christian Hospital, Changhua

Changhua Hosiptal Ministry of Health And Welfare, Changhua

Chang Gung Memorial Hospital, ChiaYi, Chiayi City

Chang Gung Memorial Hospital, Kaohsiung, Kaohsiung City

E-DA Hospital, I-Shou University, Kaohsiung City

Kaohsiung Medical University Hospital, Kaohsiung City

Kaohsiung Veterans General Hospital, Kaohsiung City

Chang Gung Memorial Hospital ,Linkou, Linkou District

Taichung Veterans General Hospital, Taichung

Buddhist Tzu Chi General Hospital, Taipei

Cheng Hsin General Hospital, Taipei

National Taiwan University Hospital, Taipei

Taipei City Hospital, Taipei

Taipei Medical University Hospital, Taipei

Taipei Medical University-Shuang Ho Hospital, Taipei

Taipei Wanfang Hospital, Taipei

All Listed Sponsors
collaborator

National Defense Medical Center, Taiwan

OTHER

collaborator

National Research Program for Biopharmaceuticals, Taiwan

OTHER

lead

Orient Pharma Co., Ltd.

INDUSTRY

NCT02467608 - Efficacy of HUEXC030 in Subjects With Pulmonary Tuberculosis | Biotech Hunter | Biotech Hunter