Clinical Trial to Evaluate the Efficacy and Safety of EEC for the Diagnosis of Mycobacterium Tuberculosis Infection in People Aged 3 Years and Above

PHASE3RecruitingINTERVENTIONAL
Enrollment

1,784

Participants

Timeline

Start Date

August 9, 2025

Primary Completion Date

May 1, 2026

Study Completion Date

July 1, 2026

Conditions
Tuberculosis
Interventions
BIOLOGICAL

5μg/ml EEC

0.1ml, one time, containing high dose 5μg/ml of active ingredients

BIOLOGICAL

5 unit(U) EC

0.1 ml , one time, containing 5U of active ingredients

BIOLOGICAL

5 IU TB-PPD

0.1 ml , one time, containing 5IU of active ingredients

DIAGNOSTIC_TEST

IGRA

96-well/plate x 2 plates; 100 tubes/box x 1 box

Trial Locations (8)

101149

RECRUITING

Beijing Chest Hospital, Beijing

410006

RECRUITING

Changsha Center Hospital, Hunan

430000

RECRUITING

Wuhan Pulmonary Hospital, Wuhan

610066

RECRUITING

Public health clinical center of chengdu, Chengdu

Unknown

RECRUITING

LiuZhou People's Hospital, Liuzhou

NOT_YET_RECRUITING

The First Affiliated Hospital of Xinxiang Medical College, Xinxiang

RECRUITING

Wuhan Central Hospital, Wuhan

RECRUITING

Yichang Central People's Hospital, Yichang

All Listed Sponsors
collaborator

Beijing Chest Hospital, Capital Medical University

OTHER

collaborator

Wuhan Pulmonary Hospital

OTHER

collaborator

Changsha Central Hospital

OTHER

collaborator

The First Affiliated Hospital of Xinxiang Medical College

OTHER

collaborator

LiuZhou People's Hospital

OTHER

collaborator

Wuhan Central Hospital

OTHER

collaborator

Yichang Central People's Hospital

OTHER

lead

Chengdu CoenBiotech Co., Ltd

INDUSTRY

NCT07152639 - Clinical Trial to Evaluate the Efficacy and Safety of EEC for the Diagnosis of Mycobacterium Tuberculosis Infection in People Aged 3 Years and Above | Biotech Hunter | Biotech Hunter