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
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.
For more information, please contact Incyte Corporation at 1.855.463.3463
Condition | Urothelial Tract Cancer, Metastatic Cancer |
---|---|
Clinical Study Identifier | TX152594 |
Sponsor | Incyte Corporation |
Last Modified on | 21 April 2022 |
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