RecruitingPhase 3NCT07152639
Clinical Trial to Evaluate the Efficacy and Safety of EEC for the Diagnosis of Mycobacterium Tuberculosis Infection in People Aged 3 Years and Above
Studying Tuberculosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Chengdu CoenBiotech Co., Ltd
- Intervention
- 5μg/ml EEC(biological)
- Enrollment
- 1784 enrolled
- Eligibility
- 3 years · All sexes
- Timeline
- 2025 – 2026
Study locations (8)
- Beijing Chest Hospital, Beijing, Beijing Municipality, China
- Changsha Center Hospital, Hunan, Changsha, China
- LiuZhou People's Hospital, Liuchow, Guangxi, China
- The First Affiliated Hospital of Xinxiang Medical College, Xinxiang, Henan, China
- Wuhan Pulmonary Hospital, Wuhan, Hubei, China
- Wuhan Central Hospital, Wuhan, Hubei, China
- Yichang Central People's Hospital, Yichang, Hubei, China
- Public health clinical center of chengdu, Chengdu, Sichuan, China
Collaborators
Beijing Chest Hospital, Capital Medical University · Wuhan Pulmonary Hospital · Changsha Central Hospital · The First Affiliated Hospital of Xinxiang Medical College · LiuZhou People's Hospital · Wuhan Central Hospital · Yichang Central People's Hospital
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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