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Brief Title: A Study to Evaluate TAR-210 Versus Single Agent Intravesical Cancer Treatment in Participants With Bladder Cancer
Official Title: A Phase 3, Randomized Study Evaluating the Efficacy and Safety of TAR-210 Erdafitinib Intravesical Delivery System Versus Single Agent Intravesical Chemotherapy in Participants With Intermediate-risk Non-muscle Invasive Bladder Cancer (IR-NMIBC) and Susceptible FGFR Alterations
Study ID: NCT06319820
Brief Summary: The main purpose of this study is to compare the disease-free survival between participants receiving treatment with TAR-210 versus investigator's choice of intravesical chemotherapy for treatment of intermediate-risk NMIBC.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Arkansas Urology, Little Rock, Arkansas, United States
Genesis Research LLC, Los Alamitos, California, United States
Genesis Research LLC, Sherman Oaks, California, United States
First Urology, Jeffersonville, Indiana, United States
Associated Medical Professionals of Ny, Syracuse, New York, United States
MidLantic Urology, Bala-Cynwyd, Pennsylvania, United States
Keystone Urology Specialists, Lancaster, Pennsylvania, United States
Urology Associates, Nashville, Tennessee, United States
Urology Austin, Austin, Texas, United States
Hadassah University Hospita - Ein Kerem, Jerusalem, , Israel
Name: Johnson & Johnson Enterprise Innovation Inc. Clinical Trial
Affiliation: Johnson & Johnson Enterprise Innovation Inc.
Role: STUDY_DIRECTOR