Clinical trial · Interventional
9MW2821 in Combination With Toripalimab vs Standard Chemotherapy in Locally Advanced or Metastatic Urothelial Cancer
A Randomized, Controlled, Open-label, Multicenter Phase 3 Clinical Study of 9MW2821 in Combination With Toripalimab Versus Standard Chemotherapy in First-line Locally Advanced or Metastatic Urothelial Cancer
NCT06592326CI-TRIAL-00080560recruitingPhase 3ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Urothelial Carcinoma | Urothelial Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 9MW2821 | Drug | — | UNRESOLVED |
| Cisplatin/Carboplatin | Drug | — | UNRESOLVED |
| Gemcitabine | Drug | Gemcitabine | ALIAS |
| Toripalimab | Drug | Toripalimab | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- 9MW2821+Toripalimab
- description
- 9MW2821+Toripalimab
- interventionNames
- Drug: 9MW2821
- Drug: Toripalimab
- type
- ACTIVE_COMPARATOR
- label
- Gemcitabine+Cisplatin/Carboplatin
- description
- Gemcitabine+Cisplatin/Carboplatin
- interventionNames
- Drug: Gemcitabine
- Drug: Cisplatin/Carboplatin
Primary outcomes (2)
- measure
- BICR-PFS
- timeFrame
- up to 50 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: * Sign the informed consent form approved by IEC. * Male or female subjects aged 18 to 80 years. * ECOG status: 0 or 1. * Histologically confirmed local advanced or metastatic urothelial cancer * Previously untreated with local advanced or metastatic urothelial cancer * At least one measurable lesion, according to RECIST V1.1. * Adequate tumor tissues submitted for test * Suitable for cisplatin/carboplatin-based chemotherapy assessed by investigator * Life expectancy for more than 12 weeks. * Adequate organ functions. * Proper contraception methods. * Willingness to follow the study procedures. Exclusion Criteria: * History of another malignancy within 3 years. * History of autoimmune disease requiring systemic treatment within 2 years. * History of clinically significant cardiac/cerebrovascular diseases or thrombosis within 6 months. * Major surgery treated within 28 days; Any live vaccines got within 28 days; Radiotherapy or Intravesical therapy treated within 21 days; Traditional Chinese medicine or any potent CYP3A4 inducers/inhibitors taken within 14 days. * Lots of pleural fluid and ascites, uncontrolled bone pain or spinal compression existed within 14 days; Systemic treatment with active infection within 7 days. * Previously treated with PD-1, PD-L1, PD-L2, CTLA-4 inhibitors; Previously treated with ADCs which target Nectin-4 or are conjugated with payload MMAE; Organ transplantation or allogeneic hematopoietic stem cell transplantation in the past. * Clinical significantly toxicity Grade ≥ 2 (except alopecia and pigmentation) related to previous treatment. * Any situations adding the risk of severe dry eye, active keratitis or corneal ulcer, etc. * Peripheral neuropathy Grade ≥ 2. * Any other serious chronic or uncontrolled disease. * Uncontrolled central nervous system metastases or carcinomatous meningitis. * Active HBV/HCV/HIV infection, etc. * Known allergic sensitivity to any of the ingredients of the study drug. * History of drug abuse or mental illness. * Other conditions unsuitable into the study.
References
Publications (1)
- DERIVEDZhang J, Liu R, Wang S, Feng Z, Yang H, Gao S, Li X, Yao X, Chen J, Gong Z, Li Y, Li X, Wang S, Hu C, Liu J, Zhang M, Yuan F, Shi B, Lou H, Zhao P, Qiu F, Guo H, Hu B, Xu D, Huang H, Zhang X, Feng M, Wang X, Li G, Liu D, Chen X, Wang P. Bulumtatug Fuvedotin (BFv, 9MW2821), a next-generation Nectin-4 targeting antibody-drug conjugate, in patients with advanced solid tumors: a first-in-human, open-label, multicenter, phase I/II study. Ann Oncol. 2025 Aug;36(8):934-943. doi: 10.1016/j.annonc.2025.04.009. Epub 2025 Apr 25. PMID 40288679