The main purpose of this study is to assess efficacy and safety of pirtobrutinib in participants with relapsing multiple sclerosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Administered orally
Administered orally
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
New T1 Gadolinium (Gd)-enhancing Lesions on Brain Magnetic Resonance Imaging (MRI) Per Scan
Time frame: Week 8 and Week 12
Number of New and/or Enlarging T2 Lesions
Time frame: Week 12
Total Number of T1 Gd-Enhancing Lesions Per Scan
Time frame: Week 8 and Week 12
Total Number of Gd-Enhancing Lesions Per Scan
Time frame: Week 8 and Week 12
Pharmacokinetics (PK): Plasma Concentration of Pirtobrutinib
Time frame: Baseline to Week 12
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