drugset / Trial / NCT01393106

Safety and Efficacy of Idelalisib in Relapsed or Refractory Hodgkin Lymphoma

NCT01393106

Phase 2 Completed 25 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the efficacy and safety of idelalisib in participants with relapsed of refractory Hodgkin Lymphoma (HL). The primary objective will be to assess the overall response rate. Eligible participants will initiate oral therapy with idelalisib at a starting dose of 150 mg twice daily. Treatment with idelalisib will continue until tumor progression or unacceptable toxicity.

Timeline

Start
2011-09
Primary completion
2014-08
Completion
2014-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Idelalisib Small molecule 150 mg Oral
Subject Idelalisib Small molecule 300 mg Oral

Indications