- A Study to Investigate the Efficacy and Safety of Rilzabrutinib in Adult Participants With Graves’ Disease — Recruiting • Phase II • NCT06984627.
- A trial testing whether rilzabrutinib improves Graves' disease symptoms and safety over 16 weeks in two dose groups.
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This is a parallel group, Phase 2, 2-arm study to measure the treatment effect and safety of rilzabrutinib dose 1 or rilzabrutinib dose 2 in participants with Graves' disease, with and without Graves' orbitopathy, aged 18 years or older. Study details include: * Screening period (up to 4 weeks). * Treatment period (up to 16 weeks). * Follow-up period (4 weeks). The number of visits will be up to 13. Conditions: Graves' Disease Interventions: Rilzabrutinib dose 1, Rilzabrutinib dose 2 Lead Sponsor: Sanofi Planned Enrollment: 30 participants