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Ensayo clinico de investigación para evaluar ro7567132 con o sin atezolizumab (tecentriq®) en participantes con tumores sólidos que son inoperables y/o se han diseminad

THE PURPOSE OF THIS STUDY IS TO TEST WHETHER RO7567132, GIVEN AT DIFFERENT DOSES ALONE OR IN COMBINATION WITH ANOTHER DRUG CALLED ATEZOLIZUMAB, HAS ANY EFFECT (GOOD OR BAD), AS WELL AS WHAT HAPPENS TO RO7567132 ONCE IT IS IN THE BODY AND WHAT RO7567132 ALONE OR IN COMBINATION WITH ATEZOLIZUMAB DOES IN THE BODY AND THE TUMOR.

Cancer Center
Status
In recruitment
headquarters
Pamplona/Madrid
Early phase

Technical Summary

  • MULTICENTER, OPEN-LABEL, RANDOMIZED, DOSE-ESCALATION PHASE I STUDY TO EVALUATE THE SAFETY, PHARMACOKINETICS, PHARMACODYNAMICS, AND ANTITUMOR ACTIVITY OF RO7567132 AS A SINGLE AGENT AND IN COMBINATION WITH ATEZOLIZUMAB IN PARTICIPANTS WITH ADVANCED AND/OR METASTATIC SOLID TUMORS.
  • Code EudraCT: 2024-512839-70-00
  • Protocol number: BP44956
  • Promoter: Roche Farma, S.A.
  • Molecule/Drug: RO7567132

* 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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