drugset / Trial / NCT02546544

Summary

This is an international, multi-centre, single arm Bayesian designed phase 2 study to identify and determine the safety and activity of anti-IGF-1/IR inhibition in patients with relapsed and/or refractory ESFT. Approximately 40 patients will be recruited from 5-7 European centres. Each patient will be treated with single agent linsitinib, 600 mg orally once a day for days 1-3, 8-10 and 15-17 on a 21 day cycle until disease progression or undue toxicity.

Timeline

Start
2014-03
Primary completion
2016-07-15
Completion
2016-07-15

Drugs

EvaluationDrugModalityDoseRoute
Subject linsitinib Small molecule 600 mg Oral

Indications