RecruitingPhase 1Phase 2NCT06439485

Phase I/II Trial of Pemigatinib in Combination With Atezolizumab and Bevacizumab for Treatment of Advanced Cholangiocarcinoma With FGFR2 Fusion


Sponsor

M.D. Anderson Cancer Center

Enrollment

25 participants

Start Date

Nov 19, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

To learn if pemigatinib in combination with atezolizumab and bevacizumab can help to control cholangiocarcinoma.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This Phase I/II study tests a three-drug combination — pemigatinib (a targeted therapy blocking the FGFR2 gene), atezolizumab (an immunotherapy), and bevacizumab (a drug that cuts off blood supply to tumors) — for advanced bile duct cancer (cholangiocarcinoma) that carries a specific FGFR2 gene fusion, after failure of standard chemotherapy. **You may be eligible if...** - You are 18 or older with confirmed advanced or metastatic bile duct cancer - Your tumor has an FGFR2 gene fusion or rearrangement confirmed by a validated test - Your cancer has progressed on or you refused/could not tolerate first-line chemotherapy (including gemcitabine-based therapy) - You have at least one measurable tumor - Your overall health is good (ECOG performance status 0–1) - Your blood counts and organ function meet study requirements **You may NOT be eligible if...** - Your cancer has spread to the eye (retinal detachment or other retinal pathology) - You have active autoimmune disease requiring treatment - You have uncontrolled infection or active hepatitis B or C - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPemigatinib

Given by PO

DRUGAtezolizumab

Given by PO and IV

DRUGBevacizumab

Given by PO and IV


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06439485


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