CompletedPhase 3NCT05039190
Evaluate the Efficacy and Safety of HBM9161(HL161)Subcutaneous Injection in Patients With Generalized 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)(drug)
- Enrollment
- 132 enrolled
- Eligibility
- 18-99 years · All sexes
- Timeline
- 2021 – 2023
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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