A Phase 3 interventional study of 9MW2821 and Toripalimab in Urothelial Carcinoma, sponsored by Mabwell (Shanghai) Bioscience Co., Ltd.. Recruiting at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2024-09-19.
Sponsored by Mabwell (Shanghai) Bioscience Co., Ltd. · Phase 3, Interventional, and Treatment
This is a randomized, controlled, open-label, multicenter phase 3 clinical study to evaluate the efficacy, safety and immunogenicity of 9MW2821 combined with Toripalimab versus standard chemotherapy in first-line locally advanced or metastatic urothelial cancer.
The study is planning to enroll approximately 460 participants with unresectable locally advanced or metastatic urothelial cancer who have not previously received systematic treatment.
716 studies on the registry are indexed under Carcinoma, Transitional Cell; 201 are open to participants now.
This study's planned enrollment of 460 is above the median of 49 across 549 interventional studies indexed under Carcinoma, Transitional Cell.
Browse Carcinoma, Transitional Cell studies →Mabwell (Shanghai) Bioscience Co., Ltd. is the lead sponsor of 53 studies on the registry; 25 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
9MW2821+Toripalimab
Drug: 9MW2821 · Drug: Toripalimab
Gemcitabine+Cisplatin/Carboplatin
Drug: Gemcitabine · Drug: Cisplatin/Carboplatin
9MW2821, 1.25mg/kg, intravenous (IV) infusion
Toripalimab, 240mg, intravenous (IV) infusion
Also known as: Toripalimab injection
Gemcitabine: 1000mg/m2, intravenous (IV) infusion
Also known as: Gemcitabine Hydrochloride for Injection
Cisplatin: 70mg/m2 or Carboplatin: AUC=4.5/5, intravenous (IV) infusion.
Also known as: Cisplatin for injection/Carboplatin Injection
BICR-PFS
Progression-free survival, assessed by BICR
Time frame: up to 50 months
OS
Overall Survival
Time frame: up to 50 months
ORR
Objective response rate, assessed by BICR or investigator
Time frame: Up to 50 months
DCR
Disease control rate, assessed by BICR or investigator
Time frame: Up to 50 months
DoR
Duration of response, assessed by BICR or investigator
Time frame: Up to 50 months
PFS
Progression-free survival, assessed by investigator
Time frame: Up to 50 months
AE/SAE
Adverse event, serious adverse event
Time frame: Up to 50 months
Immunogenicity
Anti-Drug Antibody (ADA) of 9MW2821
Time frame: Up to 50 months
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
Contact study teamGet an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Mabwell (Shanghai) Bioscience Co., Ltd.