Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, 510060, China
Location status: Recruiting
NCT Number: NCT07314723
This is a single arm, open-label, multicenter phase II clinical study to evaluate the safety and efficacy of 9MW2821 combined with Toripalimab in perioperative patients with urothelial cancer.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Guangzhou, Guangdong, 510060, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
9MW2821, 1.25mg/kg, intravenous (IV) infusion
Toripalimab, 240mg, intravenous (IV) infusion
Time frame: Up to 24 months
Pathological complete response
Time frame: Up to 24 months
Clinical complete response
Time frame: Up to 24 months
Clinical objective response rate
Time frame: Up to 24 months
Time frame: Up to 24 months
Disease-free survival
Time frame: Up to 24 months
Time frame: Up to 24 months
Progression-free survival
Time frame: Up to 24 months
Overall Survival
Time frame: Up to 24 months
Adverse event, serious adverse event
Time frame: Up to 24 months
Anti-Drug Antibody (ADA) of 9MW2821
Time frame: Up to 24 months
Interested in participating?
Request InfoMabwell (Shanghai) Bioscience Co., Ltd.
Industry
A Single Arm, Open-label, Multicenter, Phase II Clinical Study to Evaluate the Safety and Efficacy of 9MW2821 Combined With Toripalimab in Perioperative Patients With Urothelial Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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