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Long Term Safety and Efficacy Study of Tolebrutinib (SAR442168) in Participants With Relapsing Multiple Sclerosis

Completed · Phase 2 · NCT03996291

Conditions: Relapsing Multiple Sclerosis

At a glance

Research payments reported, 2025
$102,579
U.S. investigators named
6
Sites paid
6
Planned or actual enrollment
125

About the trial

Sponsor
Sanofi
Tested
Tolebrutinib (drug)
Dates
Started 2019-09-23; completion 2024-11-26
Results posted
Yes

Primary Objective: To determine the long-term safety and tolerability of SAR442168 in RMS participants Secondary Objective: To evaluate efficacy of SAR442168 on disease activity, assessed by clinical and imaging methods

From ClinicalTrials.gov, last updated 2025-10-23. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Genzyme Corporation reported $102,579 in research payments for this study in 2025 (11 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • Neurology Associates, PA $77,492
  • Consultants in Neurology, Ltd $11,370
  • University of Cincinnati Physicians Company Llc $5,498
  • Sibyl Wray MD Neurology PC $3,069
  • $2,500
  • University of South Florida $1,650
  • 0000203566 North Central Neurology Assocs PC $1,000

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.