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The study is enrolling participants to see if the disitamab vedotin works to treat bladder cancer when used alone or when it is used in combination with pembrolizumab.

Age & Gender

  • 18 years ~ 99 years
  • Male, Female, Gender Inclusive

Visit Availability

  • Standard business hours (M-F, 8-5)

Location

United States (Nationwide)

What will be asked of you

The study includes blood draws, CT and/or MRI's, ECG's and completion of questionnaires.

Incentives

Possible travel reimbursement.

In-person visits:
More than 10.
Total length of participation:
Up to 3 years.

Looking for Specific Volunteers

Able to participate:

  • You are at least 18 years old.
  • You have been diagnosed with bladder cancer
  • Your bladder cancer has spread to nearby tissue or other parts of the body.

Not eligible if:

  • You have received antitumor treatment (chemotherapy, radiotherapy, targeted therapy, etc.)
  • You have participated in another clinical study within 2 weeks prior to the start of the study.
  • Known hypersensitivity to disitamab vedotin or pembrolizumab.
  • You have an acute, chronic or symptomatic infection.

Contact the Team

Visit Location

Contact & Visit Location

Primary Contact

Primary Visit Location

UNC Hospitals / UNC Medical Center
101 Manning Dr, Chapel Hill, NC 27514, USA

Additional Study Information

Principal Investigator

Matthew Milowsky
LCCC - Clinical Trials

Study Type

Clinical or Medical
Interventional

Study Topics

Cancer (Bladder)

IRB Number

24-0407

ClinicalTrials.gov

NCT04879329

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