Overview

Study of Axitinib (AG-013736) With Evaluation of the VEGF-pathway in Pheochromocytoma/Paraganglioma

Status:
Recruiting
Trial end date:
2024-01-01
Target enrollment:
Participant gender:
Summary
Primary Objective: To determine the response rate (RR) of metastatic or locally advanced pheochromocytoma/paraganglioma to axitinib administered daily. Secondary Objectives: - Determine the progression-free survival. - In an exploratory manner examine the extent of activation of the VEGFR pathway in pheochromocytoma/paraganglioma using a semi-quantitative immunohistochemistry assay and examine the relationship with response to therapy. - Perform pharmacogenomics analyses of drug metabolism and transport proteins through germline DNA examination.
Phase:
Phase 2
Details
Lead Sponsor:
Columbia University
Collaborator:
Pfizer
Treatments:
Axitinib