Clinical trial
A Randomized , Open Label, Three Arm, Parallel Group, Single Dose, Comparative Pharmacokinetic , Safety, and Immunogenicity Study Comparing KSHB002 (Abatacept) 125 mg/ ml Pre-filled Injection With US-Licenced ORENCIA and EU-Approved ORENCIA Administered Through Subcutaneous Route in Healthy Adult Human Volunteers
NCT06929039 is registered in ClinicalTrials.gov with Kashiv BioSciences, LLC as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomized , Open Label, Three Arm, Parallel Group, Single Dose, Comparative Pharmacokinetic , Safety, and Immunogenicity Study Comparing KSHB002 (Abatacept) 125 mg/ ml Pre-filled Injection With US-Licenced ORENCIA and EU-Approved ORENCIA Administered Through Subcutaneous Route in Healthy Adult Human Volunteers
- Lead sponsor
- Kashiv BioSciences, LLC
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- July 4, 2024
- Completion date
- February 25, 2025
- Enrollment
- 300 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
rheumatoid arthritis (ra