Status: Recruiting
Remibrutinib Open Label Roll-over Post-trial Access Protocol
Multi-center, open-label roll-over post-trial access protocol to provide remibrutinib treatment and collect long-term safety for up to three years for participants who are currently receiving remibrutinib treatment in a Novartis-sponsored study, who are benefiting from treatment with remibrutinib, and are unable to access remibrutinib treatment outside of a clinical study.
Participants needed: 648
Trial details
Phase: Phase 3Age: 18-100Biological sex: AllType: InterventionalSponsor: Novartis PharmaceuticalsUpdated: Aug 19, 2026Locations: 36
Eligibility criteria
Participant is deriving benefit from remibrutinib, investigator believes he/she... [+1]
Participant has prematurely discontinued study treatment in the parent study. [+1]