drugset / Trial / NCT00930514

A Pharmacokinetic Study of Subcutaneous and Intravenous Rituximab in Participants With Follicular Lymphoma

NCT00930514 ↗

Phase 1 Completed 281 enrolled Hoffmann-La Roche
Parallel-groupOpen-labelTreatment

Summary

This 2 stage study will compare the pharmacokinetics and safety profile of subcutaneous and intravenous rituximab in participants with follicular lymphoma. In the first stage, participants who have achieved at least a partial response after induction treatment with intravenous rituximab will be randomized to one of 3 treatment cohorts, to receive rituximab 375 milligram per square meter (mg/m\^2) intravenously, 375 mg/m\^2 subcutaneously or 625 mg/m\^2 subcutaneously, and pharmacokinetics evaluated on an ongoing basis. Upon selection of the subcutaneous dose (800 mg/m\^2) which results in rituximab trough plasma concentration (C trough) values comparable to those achieved with the intravenous formulation, participants in the second stage of the study will be randomized to receive either the subcutaneous or intravenous formulation to demonstrate comparability of the C trough levels with both routes of administration. Maintenance therapy will continue every 2 or 3 months with the subcutaneous formulation.

Timeline

Start
2009-09
Primary completion
2013-07
Completion
2013-07

Outcome

Met primary endpoint

paper Noninferiority (ie, meeting the prespecified 90% CI lower limit of 0.8) was then confirmed in stage 2 PMID 24821885 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody 375 mg/m2 Subcutaneous
Subject Rituximab Monoclonal antibody 625 mg/m2 Subcutaneous
Subject Rituximab Monoclonal antibody 800 mg/m2 Subcutaneous
Subject Rituximab Monoclonal antibody 1400 mg Subcutaneous

Indications