CompletedPhase 1NCT05328557
A Phase Ia Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneously Administered CUG252 in Normal Healthy Volunteers
Studying Systemic lupus erythematosus
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
- Cugene Inc.
- Principal Investigator
- Martin K Kankam, MD, PhDAltasciences Company Inc.
- Intervention
- CUG252(drug)
- Enrollment
- 32 enrolled
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2021 – 2022
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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