drugset / Trial / NCT00590603

Trisenox, Ascorbic Acid and Bortezomib in Patients With Relapsed/Refractory Multiple Myeloma

NCT00590603

Phase 1 Terminated 25 enrolled Duke University Cephalon · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a phase I dose escalation study to estimate the maximum tolerated dose (MTD) of the novel combination of Arsenic, Ascorbic Acid and Velcade, followed by a phase II study conducted using the MTD estimated from the phase I portion.

Timeline

Start
2008-07
Primary completion
2012-12
Completion
2012-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 1 mg/m2 Intravenous
Subject Vitamin C Other / unclassified 1000 mg Intravenous
Subject arsenic trioxide Small molecule 0.25 mg/kg Intravenous

Indications