Study of CKD-215 and D215 in Adults With BRCA-mutated Advanced Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexFemale
Age19-75
SponsorChong Kun Dang Pharmaceutical

About this trial

Clinical Trial to evaluate the pharmacokinetic Characteristics, safety and Tolerability among CKD-215 and D215

Eligibility criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • CKD-215
  • D215

Treatment groups

24 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators