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Clinical trial to determine the dose of Pirtobrutinib in adults with immune thrombocytopenia

THE MAIN OBJECTIVE IS TO ENSURE THE SAFETY AND EFFICACY OF PIRTOBRUTINIB IN PATIENTS WITH IMMUNE THROMBOCYTOPENIA, AND TO SELECT THE DOSES FOR PART 2 OF THIS STUDY.

Cancer Center
Status
In recruitment
headquarters
Pamplona/Madrid

Technical Summary

  • PHASE I/II DOSE-FINDING STUDY INVESTIGATING THE SAFETY AND EFFICACY OF PYRTOBRUTINIB IN ADULTS WITH IMMUNE THROMBOCYTOPENIA
  • Code EudraCT: 2024-518502-40-00
  • Protocol number: J2N-MC-JZNZ
  • Promoter: Lilly
  • Molecule/Drug: Pirtobrutinib
  • Link to Clinical Trials

* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.

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