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Clinical trial to evaluate the efficacy and safety of adjuvant Giredestrant compared to physician-choice adjuvant endocrine monotherapy in patients with estrogen receptor-positive, HER2-negative early breast cancer.
THE PURPOSE OF THIS STUDY IS TO COMPARE THE EFFECTS, POSITIVE OR NEGATIVE, OF GIREDESTRANT WITH THOSE OF AN APPROVED ENDOCRINE TREATMENT (TREATMENT THAT BLOCKS OR REMOVES HORMONES) IN PATIENTS WITH YOUR TYPE OF CANCER. IN THIS STUDY YOU WILL RECEIVE GIREDESTRANT OR A DRUG CHOSEN SPECIFICALLY FOR YOU BY THE STUDY DOCTOR.
- PHASE III, MULTICENTER, RANDOMIZED, OPEN-LABEL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ADJUVANT GIREDESTRANT COMPARED TO PHYSICIAN-CHOICE ADJUVANT ENDOCRINE MONOTHERAPY IN PATIENTS WITH ESTROGEN RECEPTOR-POSITIVE, HER2-NEGATIVE EARLY BREAST CANCER.
- Code EudraCT: 2021-000129-28
- Protocol number: GO42784
- Promoter: F. Hoffmann-La Roche Ltd.
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* 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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