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NCT Number: NCT07314723

9MW2821 Combined With Toripalimab in Perioperative Patients With Urothelial Cancer

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, 510060, China

Location status: Recruiting

Location contact

Zhuowei Liu, Professor

CONTACT

[email protected]

86-20-87343606

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • Prior systemic anti-tumor therapy for urothelial cancer.
  • Previously treated with PD-1/PD-L1 inhibitors or antibody-drug conjugates (ADCs).
  • 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.
  • Major surgery treated within 28 days; Cystoscopy/ureteroscopy biopsy or intravesical instillation therapy within 7 days.
  • Peripheral neuropathy Grade ≥ 2.
  • 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.
  • 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.
  • 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.

Treatment and study plan

9MW2821

Drug

9MW2821, 1.25mg/kg, intravenous (IV) infusion

Toripalimab Injection

Drug

Toripalimab, 240mg, intravenous (IV) infusion

Primary outcomes

  1. pCR (Arm 1 and 2)

    Time frame: Up to 24 months

    Pathological complete response

  2. cCR (Arm 3)

    Time frame: Up to 24 months

    Clinical complete response

Secondary outcomes

  1. cORR

    Time frame: Up to 24 months

    Clinical objective response rate

  2. Pathological downstaging rate (Arm 1 and 2)

    Time frame: Up to 24 months

  3. DFS (Arm 1 and 2)

    Time frame: Up to 24 months

    Disease-free survival

  4. Duration of clinical complete response (Arm 3)

    Time frame: Up to 24 months

  5. PFS (Arm 3)

    Time frame: Up to 24 months

    Progression-free survival

  6. OS

    Time frame: Up to 24 months

    Overall Survival

  7. AE/SAE

    Time frame: Up to 24 months

    Adverse event, serious adverse event

  8. Immunogenicity

    Time frame: Up to 24 months

    Anti-Drug Antibody (ADA) of 9MW2821

  9. Nectin-4 and PD-L1 expression

    Time frame: Up to 24 months

Study contacts

Contact information is provided by the study sponsor or research team.

Zhuowei Liu, Professor

CONTACT

[email protected]

86-20-87343606

Sponsors and collaborators

Lead sponsor

Mabwell (Shanghai) Bioscience Co., Ltd.

Industry

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Jan 2, 2026
Registry last updated
Jan 2, 2026

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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