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Study of ro7284755 administered alone or in combination with atezolizumab in participants with advanced solid tumors

THE MAIN OBJECTIVES OF THIS STUDY ARE AS FOLLOWS: - TO EVALUATE THE SAFETY OF DIFFERENT DOSES OF RO7284755 WHEN GIVEN ALONE OR IN COMBINATION WITH ANOTHER DRUG CALLED ATEZOLIZUMAB AND TO DETERMINE WHAT EFFECTS, RO7284755 HAS ON YOU. - GATHER INFORMATION TO DETERMINE WHETHER RO7284755 IS EFFECTIVE AGAINST TUMORS WHEN GIVEN ALONE OR IN COMBINATION WITH ATEZOLIZUMAB. - CHECK HOW RO7284755 IS DISTRIBUTED AND ELIMINATED FROM THE BODY WHEN GIVEN ALONE OR IN COMBINATION WITH ATEZOLIZUMAB.

Status
In recruitment
headquarters
Pamplona

Technical Summary

  • PHASE IA/IB MULTICENTER, OPEN-LABEL, RANDOMIZED, DOSE-ESCALATION AND COHORT EXPANSION STUDY TO EVALUATE THE SAFETY AND ANTITUMOR ACTIVITY OF RO7284755, AN IMMUNOCYTOKINE COMPOSED OF AN IL-2 VARIANT (IL-2V) DIRECTED AGAINST PD-1, ADMINISTERED ALONE OR IN COMBINATION WITH ATEZOLIZUMAB IN PARTICIPANTS WITH ADVANCED AND/OR METASTATIC SOLID TUMORS. IMMUNOTHERAPY
  • Code EudraCT: 2019-004022-25
  • Protocol number: BP41628
  • Promoter: Roche Farma, S.A.
  • 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.

More information about this clinical trial

Information offered by the Spanish Registry of Clinical Studies

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