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Extension trial for post-trial access to remibrutinib.

THE OBJECTIVE OF THIS TRIAL IS TO PROVIDE CONTINUED TREATMENT WITH REMIBRUTINIB AND COLLECT LONG-TERM SAFETY DATA IN PATIENTS WHO HAVE COMPLETED A NOVARTIS REMIBRUTINIB TRIAL, WHO HAVE BENEFITED FROM TREATMENT, AND WHO CANNOT OBTAIN REMIBRUTINIB LOCALLY.

Navarre headquarters
Madrid headquarters
Status
In recruitment
headquarters
Madrid

Technical Summary

  • CLINICAL TRIAL TO PROVIDE ACCESS TO REMIBRUTINIB AFTER THE TRIAL ENDS AND TO COLLECT INFORMATION ON LONG-TERM SAFETY IN PATIENTS WHO HAVE COMPLETED TREATMENT WITH REMIBRUTINIB IN A NOVARTIS TRIAL.
  • Code EudraCT: 2025-524078-4000
  • Protocol number: CLOU064A2306B
  • Promoter: Novartis Farmaceutica
  • Molecule/Drug: Remibrutinib
  • 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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