drugset / Trial / NCT00622258

A Phase I Dose Escalation Study of RAD001 Administered in Patients With Relapsed or Refractory Non-Hodgkin's Lymphoma

NCT00622258 ↗

Phase 1 Completed 13 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This study assesses the tolerability, safety, efficacy and pharmacokinetics of everolimus in Japanese patients. Everolimus is administered orally everyday to adult patients with relapsed or refractory non-Hodgkin's lymphoma who have progressed despite standard therapy or for whom standard systemic therapy dose not exist.

Timeline

Start
2008-03
Primary completion
2014-01
Completion
2014-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Everolimus Small molecule — Oral

Indications