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RecruitingNCT06592326Updated Sep 19, 2024

9MW2821 in Combination With Toripalimab vs Standard Chemotherapy in Locally Advanced or Metastatic Urothelial Cancer

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

From the registry’s dates

  • Started Aug 2024; still recruiting 2 years 1 month later.
Phase
Phase 3
Study type
Interventional
Enrollment
460
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

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.

Read the detailed description

The study is planning to enroll approximately 460 participants with unresectable locally advanced or metastatic urothelial cancer who have not previously received systematic treatment.

02

Conditions studied

  • Urothelial Carcinoma
03

In context

Carcinoma, Transitional Cell

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
460 participants (estimated)

Study arms

  • Experimental
    9MW2821+Toripalimab

    9MW2821+Toripalimab

    Drug: 9MW2821 · Drug: Toripalimab

  • Active comparator
    Gemcitabine+Cisplatin/Carboplatin

    Gemcitabine+Cisplatin/Carboplatin

    Drug: Gemcitabine · Drug: Cisplatin/Carboplatin

Interventions

  • Drug9MW2821

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

  • DrugToripalimab

    Toripalimab, 240mg, intravenous (IV) infusion

    Also known as: Toripalimab injection

  • DrugGemcitabine

    Gemcitabine: 1000mg/m2, intravenous (IV) infusion

    Also known as: Gemcitabine Hydrochloride for Injection

  • DrugCisplatin/Carboplatin

    Cisplatin: 70mg/m2 or Carboplatin: AUC=4.5/5, intravenous (IV) infusion.

    Also known as: Cisplatin for injection/Carboplatin Injection

06

What researchers measure

Primary outcomes

  1. BICR-PFS

    Progression-free survival, assessed by BICR

    Time frame: up to 50 months

  2. OS

    Overall Survival

    Time frame: up to 50 months

Secondary outcomes

  1. ORR

    Objective response rate, assessed by BICR or investigator

    Time frame: Up to 50 months

  2. DCR

    Disease control rate, assessed by BICR or investigator

    Time frame: Up to 50 months

  3. DoR

    Duration of response, assessed by BICR or investigator

    Time frame: Up to 50 months

  4. PFS

    Progression-free survival, assessed by investigator

    Time frame: Up to 50 months

  5. AE/SAE

    Adverse event, serious adverse event

    Time frame: Up to 50 months

  6. Immunogenicity

    Anti-Drug Antibody (ADA) of 9MW2821

    Time frame: Up to 50 months

07

Study locations

1 of 1 sites recruiting
  • Fudan University Shanghai Cancer Center
    Shanghai, Shanghai 200032, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06592326
Lead sponsor
Mabwell (Shanghai) Bioscience Co., Ltd.
Responsible party
Sponsor
First posted
Sep 19, 2024
Start date
Aug 22, 2024
Primary completion
Sep 2027 (estimated)
Completion
Dec 2028 (estimated)
Last update
Sep 19, 2024

Study contacts

Dingwei Ye, Professor
Contact
fuscc2012@163.com
13701663571

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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