drugset / Trial / NCT01789723

Phase 1 Study of Fusilev to Prevent or Reduce Mucositis in Patients With Non-Hodgkin's Lymphoma Receiving Folotyn

NCT01789723

Phase 1 Withdrawn Acrotech Biopharma Inc.
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is determine the optimal dose and schedule of Fusilev to prevent or reduce Mucositis in patients with Non-Hodgkin's Lymphoma receiving Folotyn treatment.

Timeline

Start
2013-03
Primary completion
2015-03
Completion
2015-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Levoleucovorin Unknown 5 mg/m2 Intravenous
Background Pralatrexate Other / unclassified 30 mg/m2

Indications