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Study of RO7247669, a bispecific antibody against pd1-lag3, in patients with advanced and/or metastatic solid tumors.

THE MAIN OBJECTIVE OF THIS STUDY IS TO DETERMINE THE SAFETY, TOLERABILITY, MAXIMUM TOLERATED DOSE (MTD) AND/OR RECOMMENDED DOSE FOR PHASE II (DRF2) OF RO7247669 ADMINISTERED INTRAVENOUSLY (IV) IN MONOTHERAPY.

Status
In recruitment
headquarters
Pamplona/Madrid

Technical Summary

  • MULTICENTER, OPEN-LABEL, DOSE-ESCALATION PHASE I STUDY TO EVALUATE THE SAFETY/TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS AND PRELIMINARY ANTITUMOR ACTIVITY OF RO7247669, A BISPECIFIC ANTIBODY AGAINST PD1-LAG3, IN PATIENTS WITH ADVANCED AND/OR METASTATIC SOLID TUMORS
  • Code EudraCT: 2019-000779-18
  • Protocol number: NP41300
  • Promoter: F. Hoffmann-La Roche Ltd.

* 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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