Condition: Ovarian · Primary Peritoneal · Fallopian Tube Cancer · Sponsor: Innovent Biologics (Suzhou) Co. Ltd.
This is a multiregional, multicenter, randomized, open-label, phase III study to compare the efficacy, safety, and tolerability of IBI354 monotherapy with investigator's choice of chemotherapy (paclitaxel, gemcitabine, liposomal doxorubicin, or topotecan) in patients with HER2-expressing, platinum-resistant ovarian, primary peritoneal, or fallopian tube cancer. Participants with advanced ovarian, primary peritoneal, fallopian tube cancer who have failed or are intolerant to first-line or more platinum-based chemotherapy will be randomly assigned in a 2:1 ratio to two treatment arms: Experimental Arm: IBI354 monotherapy arm, 12 mg/kg IBI354 on Day 1 of each 3-week cycle; Control Arm: Investigator's choice chemotherapy (paclitaxel, gemcitabine, liposomal doxorubicin, or topotecan)
This description comes directly from the study's public registry record.
Ya Lu · 8610-68585566 · ya.lu@innoventbio.com
Always discuss trial participation with your own doctor first.
| Affiliated Cancer Hospital of Chongqing University | Chongqing, Chongqing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06834672