A Phase 1, Open-label, Randomized, Parallel-group Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, Immunogenicity, and Device Performance of ALXN1720 (Gefurulimab) Administered Subcutaneously Using Prefilled Syringe Versus Autoinjector in Adult Healthy Participants
Latest Information Update: 25 Oct 2024
At a glance
- Drugs Gefurulimab (Primary)
- Indications Myasthenia gravis; Proteinuria
- Focus Pharmacokinetics
- Sponsors Alexion AstraZeneca Rare Disease
Most Recent Events
- 23 Oct 2024 Status changed from active, no longer recruiting to completed.
- 23 Jul 2024 Planned End Date changed from 1 Apr 2025 to 23 Oct 2024.
- 23 Jul 2024 Planned primary completion date changed from 1 Apr 2025 to 18 Sep 2024.