Trials / Recruiting
RecruitingNCT06855069
HS-20089 for Injection in Patients With Platinum-Resistant Recurrent Epithelial Ovarian Cancer
A Multi-center, Randomized, Open-label, Controlled, Phase III Clinical Study Evaluating HS-20089 vs. Investigator's Choice of Chemotherapy in the Treatment of Platinum-resistant Recurrent Epithelial Ovarian Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cancer
- Status
- Recruiting
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 468 (estimated)
- Sponsor
- Hansoh BioMedical R&D Company · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is a randomized, open-label, controlled, phase III study to evaluate the efficacy and safety of HS-20089 versus investigator's choice of chemotherapy in patients with platinum-resistant recurrent epithelial ovarian cancer.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | HS-20089 | HS-20089 dose 1 |
| DRUG | Paclitaxel | Paclitaxel dose 2 |
| DRUG | Doxorubicin | Doxorubicin dose 3 |
| DRUG | Topotecan | Topotecan dose 4 |
Timeline
- Start date
- 2025-03-13
- Primary completion
- 2027-03-07
- Completion
- 2029-03-07
- First posted
- 2025-03-03
- Last updated
- 2025-12-17
Locations
1 site across 1 country: China
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06855069. Inclusion in this directory is not an endorsement.