CI

At a glance

ClinicalIndex Comparison Record
Phase 2Unknown· 12 enrolled
Drug / intervention
tolebrutinib 60mg +1 moredrug
Likely dose
tolebrutinib 60mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04742400
NCT04742400Phase 2Unknown

A Phase 2 Clinical Trial of Tolebrutinib, a Brain-penetrant Bruton's Tyrosine Kinase Inhibitor, for the Modulation of Chronically Inflamed White Matter Lesions in Multiple Sclerosis

National Institute of Neurological Disorders and Stroke (NINDS)·interventional·Posted Feb 8, 2021·Updated Aug 13, 2024

In Brief

A Phase 2 clinical trial evaluating tolebrutinib 60mg and tolebrutinib 120mg for Multiple Sclerosis. Targeting 12 participants across 1 site.

Detailed Summary

Background: Some multiple sclerosis (MS) lesions stay inflamed for very long periods of time. This type of inflammation is not affected by any MS medications. These lesions can lead to slow worsening of MS symptoms. Researchers want to see if a new drug can help. Objective: To see if tolebrutinib can help clear inflammation in MS brain lesions. Eligibility: Adults ages 18 and older with MS who are on an anti-CD20 therapy. Design: Participants will be screened under protocol #89-N-0045. Participants will have a medical history. They will have physical and neurological exams. They will have blood and urine tests. The progression of their MS will be assessed. Participants will have MRIs of the brain. The MRI scanner is shaped like a cylinder. It uses a magnetic field and radio waves to take pictures of the body. During the MRIs, participants will lie on a table that slides in and out of the scanner. Soft padding or a coil will be placed around their head. Participants may have electrocardiograms to measure the heart s electrical activity. Participants may have lumbar punctures ( spinal taps ). A small needle will be inserted into the spinal canal in the lower back. Fluid will be collected. Some participants will take tolebrutinib pills by mouth once a day for at least 96 weeks. They will stop their anti-CD20 therapy. They will have at least 10 study visits. Some participants will not take tolebrutinib. They will stay on their anti-CD20 therapy. They will have 5 study visits. Participation will last at least 96 weeks.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2UnknownOverdue
202120222023202420252026
First PostedFeb 8, 2021
Enrollment StartApr 15, 2021
Primary CompletionJun 15, 2023
Study CompletionDec 31, 2025
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 5.4 years ago

Interventions

tolebrutinib 60mgdrug

60 mg orally

tolebrutinib 120mgdrug

120 mg orally