Overview
A Study of Pirtobrutinib (LY3527727 [LOXO-305]) Versus Placebo in Participants With Relapsing Multiple Sclerosis
Status:
Withdrawn
Withdrawn
Trial end date:
2026-02-13
2026-02-13
Target enrollment:
0
0
Participant gender:
All
All
Summary
The main purpose of this study is to assess efficacy and safety of pirtobrutinib in participants with relapsing multiple sclerosis.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Loxo Oncology, Inc.Collaborator:
Eli Lilly and CompanyTreatments:
Pirtobrutinib
Criteria
Inclusion Criteria:- Participants must have been diagnosed with relapsing MS
- Participants must have one of the following
1. at least 1 documented relapse within the previous year, or
2. at least 2 documented relapse within the previous 2 years, or
3. at least 1 active Gd-enhancing brain lesion on an MRI scan in the past 6 months
prior to screening.
Exclusion Criteria:
- Have had a diagnosis of primary progressive MS
- Have a history of another clinically significant neurological disease
- Had a relapse of MS within 30 days prior to randomization.