drugset / Trial / NCT00128921
Study of Velcade® and Bone Formation in Patients With Relapsed/Refractory Multiple Myeloma
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bortezomib | Small molecule | 0.7 mg/m2 | — |
| Subject | Bortezomib | Small molecule | 1 mg/m2 | — |
| Subject | Bortezomib | Small molecule | 1.3 mg/m2 | — |