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Clinical Trial Summary

This trial will be the first study of axitinib in children and adolescents. The primary objective of this Phase 1 trial is to determine a maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D) of axitinib in pediatric patients with refractory solid tumors. Additional objectives include measurement of pharmacokinetic and pharmacodynamic parameters, description of the toxicity profile of this agent in children and adolescents, and assessment of response within the confines of a Phase 1 trial. A standard rolling 6 design will be used for dose escalation. Further development of axitinib will focus on development of a joint cooperative group (COG/ECOG) Phase 2 study of axitinib in pediatric, adolescent and young adult translocation renal cell carcinoma.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Refractory or Recurrent Solid Tumors, Excluding CNS Tumors

NCT number NCT02164838
Study type Interventional
Source Children's Oncology Group
Contact
Status Completed
Phase Phase 1
Start date September 2014
Completion date October 19, 2017