CompletedPhase 1NCT05702983
The Safety and Tolerability of STSA-1002 Following Subcutaneous Injection in Healthy Subjects
Studying Anti-neutrophil cytoplasmic antibody-associated vasculitis
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
- Staidson (Beijing) Biopharmaceuticals Co., Ltd
- Principal Investigator
- Martin K Kankam, DoctorAltasciences Clinical Kansas, Inc.
- Intervention
- STSA-1002 subcutaneous injection(drug)
- Enrollment
- 20 enrolled
- Eligibility
- 21-57 years · All sexes
- Timeline
- 2023 – 2023
Study locations (1)
- AltaSciences Clinical Kansas, Inc, Overland Park, Kansas, United States
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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