drugset / Trial / NCT00128921

Study of Velcade® and Bone Formation in Patients With Relapsed/Refractory Multiple Myeloma

NCT00128921 ↗

Phase 2 Terminated 18 enrolled University of Arkansas
Non-randomizedSingle-groupOpen-labelPrevention

Summary

Velcade (bortezomib, PS-341) has recently been approved by the Food and Drug Administration (FDA) for the treatment of multiple myeloma for patients who have received at least one prior therapy. Velcade is a unique compound developed by scientists at Millennium Pharmaceuticals, Inc. Velcade enters cells and affects the way they divide. Cancer cells are particularly sensitive. Velcade interferes with the enzyme "proteasome" which is responsible for allowing cells to divide. When cancer cells cannot divide, they die. Velcade falls into the class of drugs known as "proteasome inhibitors."

Timeline

Start
2006-04
Primary completion
2008-02
Completion
2008-02

Outcome

Outcome not reported

Stopped (Enrollment): “study terminated due to low accrual”

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 0.7 mg/m2 —
Subject Bortezomib Small molecule 1 mg/m2 —
Subject Bortezomib Small molecule 1.3 mg/m2 —

Indications