Study of CKD-215 and D215 in Adults With BRCA-mutated Advanced Ovarian, Fallopian Tube, or Primary Peritoneal Cancer
Starting soon · Phase 1
Conditions studied: Ovarian Cancer
In brief
Clinical Trial to evaluate the pharmacokinetic Characteristics, safety and Tolerability among CKD-215 and D215
Key facts
- Study ID
- NCT07532148
- Run by
- Chong Kun Dang Pharmaceutical
- People needed
- 24
- Starts
- 2026-06-01
- Expected to finish
- 2027-08-01
- Last updated by the study team
- 2026-04-15
Who can join
Age: 19 and older, up to 75. Sex: female. Healthy volunteers: not accepted.
You may qualify 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 qualify 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
Full record on ClinicalTrials.gov
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