Expanded Access Study of TAS-120 in Patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements
APPROVED_FOR_MARKETING
Conditions studied: Advanced Cholangiocarcinoma
In brief
The objective of the study is to provide access to TAS-120 to patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements.
Key facts
- Study ID
- NCT04507503
- Run by
- Taiho Oncology, Inc.
- Last updated by the study team
- 2026-03-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Provide written informed consent.
- >18 years of age.
- Histologically confirmed, locally advanced, or metastatic, or recurrent unresectable CCA harboring FGFR2 gene rearrangements based on testing performed by a qualified (CLIA-certified) laboratory.
- Patient has failed standard therapy or standard therapy is not tolerated.
- Has measurable or non-measurable lesion(s).
- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
- Adequate organ function.
You may not qualify if…
- History and/or current evidence of non-tumor related alteration of calcium-phosphorus homeostasis.
- History and/or current evidence of clinically significant ectopic mineralization/calcification.
- History and/or current evidence of clinically significant retinal disorder confirmed by retinal examination.
- A serious illness or medical condition(s)
- Pregnant or breast-feeding female
Where it is running
- Banner MD Anderson — Gilbert, Arizona, United States
- University of California, San Francisco (UCSF) — San Francisco, California, United States
- UCLA Division of Hematology-Oncology — Santa Monica, California, United States
- Mount Sinai Center of Florida — Miami Beach, Florida, United States
- Advent Health Orlando — Orlando, Florida, United States
- University of Chicago — Chicago, Illinois, United States
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins — Baltimore, Maryland, United States
- Massachusetts General Hospital — Boston, Massachusetts, United States
- Dana Farber Cancer Institute — Boston, Massachusetts, United States
- University of Kansas Cancer Center — Lee's Summit, Missouri, United States
- Duke University Medical Center — Durham, North Carolina, United States
- Providence Portland Medical Center — Portland, Oregon, United States
- MD Anderson — Houston, Texas, United States
- Utah Cancer Specialists — Salt Lake City, Utah, United States
- Seattle Cancer Care Alliance — Seattle, Washington, United States
- Aurora Cancer care — Grafton, Wisconsin, United States
Full record on ClinicalTrials.gov
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