drugset / Trial / NCT01282424

Efficacy and Safety Study of Idelalisib in Participants With Indolent B-Cell Non-Hodgkin Lymphomas

NCT01282424 ↗

Phase 2 Completed 125 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

The primary objective will be to assess the overall response rate and to evaluate the efficacy and safety of idelalisib (IDELA; GS-1101) in participants with previously treated indolent Non-Hodgkin Lymphoma (iNHL) that is refractory both to rituximab and to alkylating-agent-containing chemotherapy. Eligible participants will initiate oral therapy with idelalisib at a starting dose of 150 mg taken twice per day. Treatment with idelalisib can continue in compliant participants as long as the study is still ongoing and the participants appear to be benefiting from treatment with acceptable safety.

Timeline

Start
2011-03-18
Primary completion
2018-05-02
Completion
2018-05-16

Outcome

Met primary endpoint

registry NUMBER Idelalisib: 57.6 (48.4 to 66.4) percentage of participants NCT01282424 ↗

registry analysis (superiority test); Idelalisib; p < 0.0001; Exact binomial test; note: The null hypothesis is ≤ 20%. NCT01282424 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Idelalisib Small molecule 150 mg Oral