Study of efficacy and safety of LEE011 ribociclib (LEE011) in combination with letrozole in patients with advanced breast cancer

Update Il y a 4 ans
Reference: EUCTR2016-002556-24

Woman and Man

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Extract

To assess the clinical benefit rate (CBR) after 24 weeks for ribociclib (LEE011) in combination with letrozole among postmenopausal women and men with hormone receptor positive, HER2- negative, advanced breast cancer who received no prior treatment for advanced disease. (70% group) To assess the clinical benefit rate (CBR) after 24 weeks for ribociclib (LEE011) in combination with letrozole and goserelin among pre-, and perimenopausal women who received no prior treatment for advanced disease as well as pre-, peri- and postmenopausal women and men with hormone receptor positive, HER2- negative, advanced breast cancer who received no more than 1 prior chemotherapy and 2 prior lines of endocrine therapy for advanced disease (30% group)


Inclusion criteria

  • HR+, HER2- advanced breast cancer

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