drugset / Trial / NCT01090414

An Extension Study for Subjects Who Are Deriving Benefit With Idelalisib (GS-1101; CAL-101) Following Completion of a Prior Idelalisib Study

NCT01090414

Phase 1/2 Terminated 202 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

This is a long-term safety extension study of idelalisib (GS-1101; CAL-101) in patients with hematologic malignancies who complete other idelalisib studies. It provides the opportunity for patients to continue treatment as long as the patient is deriving clinical benefit. Patients will be followed according to the standard of care as appropriate for their type of cancer. The dose of idelalisib will generally be the same as the dose that was administered at the end of the prior study, but may be titrated up to improve clinical response or down for toxicity. Patients will be withdrawn from the study if they develop progressive disease, unacceptable toxicity related to idelalisib, or if they no longer derive clinical benefit in the opinion of the investigator.

Timeline

Start
2010-03-22
Primary completion
2018-06-18
Completion
2018-06-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Idelalisib Small molecule 350 mg Oral