CompletedPhase 2NCT04346888
A Study to Evaluate the Efficacy, Safety and PD and PK of HBM9161 in MG Patients
Studying Adult-onset myasthenia gravis
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
- Harbour BioMed (Guangzhou) Co. Ltd.
- Principal Investigator
- Chongbo ZhaoHuashan Hospital
- Intervention
- HBM9161 Injection (680mg and 340 mg)(drug)
- Enrollment
- 30 enrolled
- Eligibility
- 18-99 years · All sexes
- Timeline
- 2020 – 2021
Study locations (1)
- Huashan Hospital, Fudan University, Shanghai, Shanghai Municipality, China
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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