NCT02082626

Study of Eribulin in Children With Cancer to Determine Safety

A Phase I Study of Eribulin, a Novel Microtubule Inhibitor, in Children With Refractory or Recurrent Solid Tumors

• Status: Terminated
• Phase: Phase 1
• Study type: Interventional
• Enrollment: 3 (actual)
• Sponsor: University of Oklahoma · Academic / Other
• Sex: All
• Age: 20 Years
• Healthy volunteers: Not accepted

Summary

This is a study for children with cancer with no curative treatment options. The investigators will be giving eribulin, a new chemotherapy agent, for the first time to children. This study is designed to determine a safe dose the investigators can give to children in larger studies. The investigators will be monitoring the children on this study for the safety of the treatment and levels of eribulin in the blood after treatment. The investigators will also study the effect of the agent on the cancer.

Detailed description

This is a phase I study of eribulin, a novel tubulin inhibitor in children with relapsed and refractory solid tumors including lymphoma. Dose escalation will be performed in a classic 3+3 design starting with 75% of the adult maximum tolerated dose (MTD). Pharmacokinetics will be done on each patient. Primary endpoint will be the pediatric MTD.

Conditions

• Pediatric Cancer
• Solid Tumors
• Lymphoma

Interventions

Type	Name	Description
DRUG	Eribulin mesylate

Timeline

• Start date: 2014-02-01
• Primary completion: 2018-06-01
• Completion: 2018-06-01
• First posted: 2014-03-10
• Last updated: 2020-03-10

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated drug study