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Brief Title: Efficacy and Safety of Pemigatinib in Participants With Solid Tumors With FGFR Mutations or Translocations (FIGHT-208)
Official Title: A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Pemigatinib in Participants With Previously Treated Locally Advanced/Metastatic or Surgically Unresectable Solid Tumors Harboring Activating FGFR Mutations or Translocations (FIGHT-208)
Study ID: NCT04003623
Brief Summary: The purpose of this study is to evaluate the efficacy and safety of pemigatinib in participants with previously treated locally advanced/metastatic or surgically unresectable solid tumors harboring activating FGFR mutations or translocations.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Compassionate Cancer Care Medical Group, Fountain Valley, California, United States
Ocala Oncology Center, Ocala, Florida, United States
Hawaii Cancer Care, Honolulu, Hawaii, United States
Illinois Cancer Care, Peoria, Illinois, United States
FMH James M Stockman Cancer Institute, Frederick, Maryland, United States
New Jersey Cancer Care and Blood Disorders, Belleville, New Jersey, United States
TriHealth, Cincinnati, Ohio, United States
Sanford Cancer Center, Sioux Falls, South Dakota, United States
Mary Crowley Cancer Center, Dallas, Texas, United States
Oncology Consultants, Houston, Texas, United States
Utah Cancer Specialists, Salt Lake City, Utah, United States
Name: Incyte Medical Monitor
Affiliation: Incyte Corporation
Role: STUDY_DIRECTOR