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Clinical trial to investigate how people with advanced cancer (solid tumors) tolerate different doses of BI 3820768.

PHASE I STUDY TO DETERMINE THE SAFETY AND TOLERABILITY OF BI 3820768 IN PATIENTS WITH ADVANCED, RELAPSED, OR TREATMENT-REFRACTORY GERM CELL TUMORS, ENDOMETRIAL CANCER, OR OVARIAN CANCER.

Cancer Center
Status
In recruitment
headquarters
Madrid
Early phase

Technical Summary

  • PHASE I STUDY TO DETERMINE THE SAFETY AND TOLERABILITY OF BI 3820768 IN PATIENTS WITH ADVANCED, RELAPSED, OR TREATMENT-REFRACTORY GERM CELL TUMORS, ENDOMETRIAL CANCER, OR OVARIAN CANCER.
  • Code EudraCT: 2025-522913-45-00
  • Protocol number: 2001-0001
  • Promoter: Boehringer Ingelheim España, S.A.
  • Molecule/Drug: BI 3820768
  • 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.

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