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Clinical trial of RMC-6291 in monotherapy in subjects with advanced solid tumors with KRAS(G12C) mutation.

THE PURPOSE OF THIS STUDY IS TO EVALUATE THE SAFETY, TOLERABILITY AND PHARMACOKINETICS (PK) OF ESCALATING DOSES OF RMC-6291 (KRAS G12C(ON) INHIBITOR) IN MONOTHERAPY IN ADULT SUBJECTS WITH ADVANCED SOLID TUMORS AND TO IDENTIFY THE MAXIMUM TOLERATED DOSE (MTD) AND RECOMMENDED PHASE 2 DOSE.

Cancer Center
Status
In recruitment
headquarters
Pamplona/Madrid
Early phase

Technical Summary

  • PHASE I/IB, MULTICENTER, OPEN-LABEL, OPEN-LABEL, STEPWISE ESCALATION AND DOSE ESCALATION STUDY OF RMC-6291 IN MONOTHERAPY IN SUBJECTS WITH ADVANCED KRAS(G12C)-MUTATED SOLID TUMORS
  • Code EudraCT: 2022-000388-35
  • Protocol number: RMC-6291-001
  • Promoter: Revolution Medicines, Inc.

* 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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