A Study of Pirtobrutinib (LY3527727 [LOXO-305]) Versus Placebo in Participants With Relapsing Multiple Sclerosis
Withdrawn before enrolling · Phase 2 · Has a placebo group
Conditions studied: Relapsing Multiple Sclerosis, Multiple Sclerosis
In brief
The main purpose of this study is to assess efficacy and safety of pirtobrutinib in participants with relapsing multiple sclerosis.
Key facts
- Study ID
- NCT06104683
- Run by
- Loxo Oncology, Inc.
- People needed
- 0
- Starts
- 2024-05-01
- Expected to finish
- 2026-02-13
- Last updated by the study team
- 2024-03-27
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participants must have been diagnosed with relapsing MS
- Participants must have one of the following
- at least 1 documented relapse within the previous year, or
- at least 2 documented relapse within the previous 2 years, or
- at least 1 active Gd-enhancing brain lesion on an MRI scan in the past 6 months prior to screening.
You may not qualify if…
- 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.
Where it is running
- University of South Florida — Tampa, Florida, United States
- Clinical Trial Network — Houston, Texas, United States
- Swedish Medical Center-501 E Hampden Ave — Seattle, Washington, United States
- Caribbean Center For Clinical Research Inc — Guaynabo, Puerto Rico
Full record on ClinicalTrials.gov
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