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Phase 3 clinical trial, to compare the efficacy and safety of MK-2870 in monotherapy versus physician's choice treatment as second-line therapy in participants with recurrent or metastatic cervical cancer.

THE MAIN OBJECTIVE IS TO EVALUATE THE SAFETY OF MK-2870.

Cancer Center
Status
In recruitment
headquarters
Madrid

Technical Summary

  • PHASE 3, RANDOMIZED, ACTIVE TREATMENT-COMPARATIVE, UNBLINDED, MULTICENTER, MULTICENTER STUDY TO COMPARE THE EFFICACY AND SAFETY OF MK-2870 IN MONOTHERAPY VERSUS TREATMENT OF PHYSICIAN'S CHOICE AS SECOND-LINE THERAPY IN PARTICIPANTS WITH RECURRENT OR METASTATIC CERVICAL CANCER (TROFUSE-020/GOG-3101/ENGOT-CX20).
  • Code EudraCT: 2023-508323-12
  • Protocol number: MK-2870-020
  • Promoter: Merck Sharp & Dohme, S.A.
  • Molecule/Drug: MK-2870

* 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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