Overview

A Study of Pirtobrutinib (LY3527727 [LOXO-305]) Versus Placebo in Participants With Relapsing Multiple Sclerosis

Status:
Withdrawn
Trial end date:
2026-02-13
Target enrollment:
0
Participant gender:
All
Summary
The main purpose of this study is to assess efficacy and safety of pirtobrutinib in participants with relapsing multiple sclerosis.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Loxo Oncology, Inc.
Collaborator:
Eli Lilly and Company
Treatments:
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.