An Open Label, Multicenter Roll-over Extension Program (REP) to Characterize the Long-term Safety and Tolerability of Iptacopan (LNP023) in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Who Have Completed PNH Phase 2 and Phase3 Studies With Iptacopan
Latest Information Update: 09 Aug 2026
At a glance
- Drugs Iptacopan (Primary)
- Indications Paroxysmal nocturnal haemoglobinuria
- Focus Adverse reactions
- Acronyms PNH-REP
- Sponsors Novartis; Novartis Pharmaceuticals
Most Recent Events
- 21 May 2026 According to a Novartis media release, data from this study will be presented at the European Hematology Association (EHA) 2026 Congress.
- 16 Apr 2026 Planned End Date changed from 19 Oct 2027 to 18 Oct 2027.
- 16 Apr 2026 Planned primary completion date changed from 19 Oct 2027 to 18 Oct 2027.