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NCT07314723RecruitingPhase 2

9MW2821 Combined With Toripalimab in Perioperative Patients With Urothelial Cancer

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

Source: ClinicalTrials.gov · Last updated 2 Jan 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
90 (estimated)
First submitted
18 Dec 2025
Start date
Aug 2025
Primary completion date
Dec 2027
Lead sponsor
Mabwell (Shanghai) Bioscience Co., Ltd.
NCT number
NCT07314723

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 90
  • From Aug 2025 to the primary completion date, Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior systemic anti-tumor therapy for urothelial cancer.
  • Previously treated with PD-1/PD-L1 inhibitors or antibody-drug conjugates (ADCs).
  • Major surgery treated within 28 days; Cystoscopy/ureteroscopy biopsy or intravesical instillation therapy within 7 days.
  • Any live vaccines got within 28 days.
  • Organ transplantation or allogeneic hematopoietic stem cell transplantation in the past.
  • Any potent CYP3A4 inducers/inhibitors taken within 14 days.

Other illness

  • 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 1 year.
  • Any situations adding the risk of severe dry eye, active keratitis or corneal ulcer, etc.
  • Active HBV/HCV/HIV infection, etc.
  • Any other serious chronic or uncontrolled disease.
  • 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.

Other

  • Peripheral neuropathy Grade ≥ 2.

Who the study is looking for

  • Sign the informed consent form approved by IEC.
  • Male or female subjects aged ≥18 years old.
  • ECOG status: 0 or 1.
  • Histologically confirmed urothelial cancer.
  • Imaging confirmed non-metastatic urothelial cancer (M0). Arm 1: MIBC, T2-4aN0-1. Arm 2: High-risk UTUC, N0. Arm 3: MIBC, T2-4aN0.
  • Adequate tumor tissues submitted for test.
  • Life expectancy for more than 12 weeks.
  • Adequate organ functions.
  • Proper contraception methods.
  • Willingness to follow the study procedures.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sun Yat-sen University Cancer Center
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.