Overview
VELCADE
®
Research and Development
Clinical Trials
Resources for Patients
MULTIPLE MYELOMA
MECHANISM
LANDMARK PHASE 3 APEX TRIAL
SURVIVAL
TREATMENT TIMING
RENAL IMPAIRMENT
LENGTH OF THERAPY
RETREATMENT
SAFETY PROFILE
-
Peripheral Neuropathy
-
Transient Thrombocytopenia
DOSE MODIFICATION GUIDELINES
HANDLING AND ADMINISTRATION
IMPORTANT SAFETY INFORMATION
REIMBURSEMENT
ADDITIONAL INFORMATION
REFERENCES
PERIPHERAL NEUROPATHY
Manageable and Generally Reversible
1
Mild preexisting peripheral neuropathy (less than grade 2) was
not predictive
of treatment-emergent peripheral neuropathy in APEX
–
69% of all patients entered the APEX trial with preexisting peripheral neuropathy*
*630 patients in APEX were assessed at baseline for presence of peripheral neuropathy.
1
†
National Cancer Institute Common Terminology Criteria (NCI CTC), Version 2.0., June 1999
2
Please
click here
to view additional important safety information.
For full Prescribing Information
click here
. (pdf) (74KB)
For further information about VELCADE
®
(bortezomib) for Injection, call
1-866-VELCADE
(
U.S. clinicians only
).
© 2008 Millennium Pharmaceuticals, Inc.
Update Notice
|
Usage Terms
|
Privacy Policy