Pemigatinib in Treating Patients With Advanced/Metastatic or Surgically Unresectable Cholangiocarcinoma Including FGFR2 Rearrangement
About the study
This is a phase 2 study to investigate the efficacy and safety of Pemigatinib in treating patients with advanced/metastatic or surgically unresectable cholangiocarcinoma with FGFR2 rearrangement who have failed at least 1 previous therapy
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
- Men and women, aged 18 or older.
- Histologically or cytologically confirmed cholangiocarcinoma which was considered to be advanced/metastatic or surgically unresectable by the investigator through image examination.
- Radiographically measurable disease per RECIST v 1.1
- Documentation of FGFR2 rearrangement.
- Documented disease progression after at least 1 line of prior systemic therapy.
- ECOG performance status of 0~1.
- Life expectancy ≥12 weeks.
EXCLUSION CRITERIA
Exclusion Criteria:
- Prior receipt of a selective FGFR inhibitor.
- History of calcium and phosphate hemostasis disorder or systemic mineral imbalance with ectopic calcification of softy tissues ( exception: skin, kidney, tendons or vessels due to injury, disease, and aging, in the absence of systemic mineral imbalance).
- Currently evidence of clinically significant corneal or retinal disorder confirmed by ophthalmologic examination.
- Use of any potent CYP3A4 inhibitors or inducers within 14 days or 5 half-lives, whichever is shorter, before the first dose of study drug. Topical ketoconazole will be allowed.
Study Locations
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How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Cholangiocarcinoma
Age (in years)
18+
Phase
Phase 2
Participants needed
34
Est. Completion Date
Dec 30, 2023
Treatment type
Interventional
Sponsor
Innovent Biologics (Suzhou) Co. Ltd.
ClinicalTrials.gov identifier
NCT04256980
Study number
CIBI375A201
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