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Study to Evaluate the Efficacy and Safety of Oral Rilzabrutinib in Adults With Immune Thrombocytopenia (ITP) Who Failed First-line Treatment

Recruiting · Phase 3 · NCT07007962

Conditions: Immune Thrombocytopenia

At a glance

Research payments reported, 2025
$11,250
U.S. investigators named
1
Sites paid
1
Planned or actual enrollment
60

About the trial

Sponsor
Sanofi
Tested
rilzabrutinib (drug)
Dates
Started 2025-10-24; completion 2028-12-30
Results posted
Not yet

This is a multinational, open label, single arm study that will evaluate the impact of early multi-immune modulation with rilzabrutinib in adult ITP patients who failed first-line treatment. The study includes a screening period (up to 8 weeks), a primary analysis period (up to 28 weeks), a long-term extension period for selected participants (28 weeks) and a 24-week follow-up period only for eligible participants.

From ClinicalTrials.gov, last updated 2026-06-22. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi US Services Inc. reported $11,250 in research payments for this study in 2025 (1 payments).

Products named: Wayrilz

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

  • Community Cancer Trials of Utah, Llc $11,250

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