Last updated on February 2019

Phase 2 Study of KHK2375 in Subjects With Advanced or Recurrent Breast Cancer

Brief description of study

The primary objective of this study is to investigate the effect of 5 mg KHK2375 on progression free survival (PFS) when administered orally at weekly intervals in combination with exemestane in a placebo-controlled, double-blind comparative study in subjects with advanced or recurrent hormone receptor-positive breast cancer. The secondary objectives are to investigate the effect of on overall survival (OS) and the antitumor effect and to evaluate the pharmacokinetics and safety.

Clinical Study Identifier: NCT03291886

Recruitment Status: Closed

Brief Description Eligibility Contact Research Team

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