Study in Healthy Subjects to Investigate the Relative Bioavailability and Safety of Pasireotide After Single Subcutaneous Dose Administration Using a Reusable ServoPen With Cartridge as Compared to Administration Using a Syringe Drawn From an Ampule
Clinical trial NCT07312643 · COMPLETED
Trial details
- NCT number
- NCT07312643
- Sponsor
- RECORDATI GROUP
- Status
- COMPLETED
- Phase
- Phase 1
- Study type
- INTERVENTIONAL
- Start date
- 2025-12-01
- Primary completion
- 2026-02-03
- Enrollment
- 40
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