A Multi-center, Randomized, Open-Label, Multiple-dose, Two-Stage, Two-treatment, Two-period, Crossover Study
Age
19–75
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Between 19 aged and 75 aged in patients with advanced BRCA-mutated high-grade epithelial ovarian cancer, fallopian tube cancer or primary peritoneal cancer
18.0kg/m2≤body mass index(BMI)≤28.0kg/m2
You may not be if
Have a gastrointestinal disease(Crohn's disease, ulcer etc.) history that can effect drug absorption or surgery
Patients with central nervous system metastases, unless clinically stable after treatment
CTCAE Grade 3 or higher adverse events(e.g., anemia, neutropenia, dysgeusia, cough, leukopenia, thrombocytopenia) related to D215
Subjects who are unable to participate in this clinical trial at the discretion of the investigator
Clareo Health | Study of CKD-215 and D215 in Adults With BRCA-mutated Advanced Ovarian, Fallopian Tube, or Primary Peritoneal Cancer
