Last updated on March 2019

A Phase 2, Open-Label, Single-Agent, Multicenter Study to Evaluate the Efficacy and Safety of INCB054828 in Subjects With Metastatic or Surgically Unresectable Urothelial Carcinoma Harboring FGF/FGFR Alterations


Brief description of study

A Phase 2, Open-Label, Single-Agent, Multicenter Study to Evaluate the Efficacy and Safety of INCB054828 in Subjects With Metastatic or Surgically Unresectable Urothelial Carcinoma Harboring FGF/FGFR Alterations

Detailed Study Description

The purpose of this study is to evaluate the overall response rate (ORR) of INCB054828 as a monotherapy in the treatment of metastatic or surgically unresectable urothelial carcinoma harboring FGF/FGFR alterations.

Clinical Study Identifier: TX152594

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Salt Lake City, UT USA
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Pittsburgh, PA USA
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Nashville, TN USA
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Milwaukee, WI USA
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San Francisco, CA USA
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Baltimore, MD USA
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Burlington, MA USA
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Las Vegas, NV USA
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New Hyde Park, NY USA
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Rochester, NY USA
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Chapel Hill, NC USA
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Cincinnati, OH USA
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Bethlehem, PA USA
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Myrtle Beach, SC USA
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Kortrijk, Belgium
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Roeselare, Belgium
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Copenhagen, Denmark
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Be'er Ya'akov, Israel
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San Giovanni Rotondo, Italy
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Amsterdam, Netherlands
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Miami Beach, FL USA
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San Diego, CA USA
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Glenwood Springs, CO USA
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Ramat Gan, Israel
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Besancon, Doubs, France
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Bordeaux, Gironde, France
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Toulouse, Haute Garonne, France
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Saint Herblain, Loire Atlantique, France
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Angers, Maine et Loire, France
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Lyon, Rhone, France
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Strasbourg, Rhone, France
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Villejuif, France
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London, Greater London, United Kingdom
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Nottingham, Nottinghamshire, United Kingdom
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Glasgow, Strathclyde, United Kingdom
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Birmingham, West Midlands, United Kingdom
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Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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