About this trial
Ovarian cancer is one of the most fatal malignant tumors that threaten women's health. The incidence rate is the third place among the female reproductive system malignant tumors, and the mortality rate ranks the first in gynecologic malignancies, the majority of patients have advanced diseases at the time of diagnosis.
This observational study is to evaluate the safety and efficacy of senaparib in ovarian cancer patients under real conditions, especially in various subgroups of ovarian cancer patients, in order to provide information about treatment modes for ovarian cancer patients in real-world diagnosis and treatment。
Eligibility criteria
Qualifiers
Sign informed consent and voluntarily join the study;
Epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer diagnosed by histology or cytology;
The investigator determined that the patient could receive senaparib monotherapy or combination therapy;
For patients with fertility, effective contraceptive methods should be used during the study period and within 90 days after the last administration of senaparib
Disqualifiers
There is evidence that the patient is a pregnant or lactating woman;
Participating in any research with intervention measures other than routine -clinical practice;
The researcher judges other situations that are not suitable for inclusion in the study;
Trial design
Treatments tested in this trial
- Senaparib capsules(20mg)