drugset / Trial / NCT00824265

Ofatumumab Added to Fludarabine-Cyclophosphamide vs Fludarabine-Cyclophosphamide Combination in Relapsed Subjects With Chronic Lymphocytic Leukemia

NCT00824265 ↗

Phase 3 Completed 365 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the safety and efficacy of ofatumumab added to fludarabine-cyclophosphamide in patients with relapsed Chronic Lymphocytic Leukemia (CLL).

Timeline

Start
2009-03-12
Primary completion
2014-12-17
Completion
2017-10-25

Outcome

Met primary endpoint

paper Median IRC-assessed PFS was 28.9 months with OFA + FC versus 18.8 months with FC (hazard ratio = 0.67; 95% confidence interval, 0.51-0.88; p = .0032). PMID 27731748 ↗

release “COMPLEMENT 2 study showed that treatment with Arzerra ® (ofatumumab) plus fludarabine and cyclophosphamide met the primary endpoint” novartis.com ↗

release “data from the Phase III COMPLEMENT 2 study showing that treatment with Arzerra ® (ofatumumab) plus fludarabine and cyclophosphamide significantly improved median progression-free survival” novartis.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ofatumumab Monoclonal antibody 1000 mg —
Comparator Cyclophosphamide Other / unclassified 250 mg/m2 —
Comparator Fludarabine Small molecule 25 mg/m2 —