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Terminated Phase 2 Interventional Results available

Alternative Schedule of Velcade/Dexamethasone Plus Doxil for Patients With Multiple Myeloma

ClinicalTrials.gov ID: NCT00366106

Public ClinicalTrials.gov record NCT00366106. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 8:40 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II, Open Label Study Evaluating an Alternative Schedule of Velcade/Dexamethasone Plus Doxil in the Treatment of Multiple Myeloma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The current study is being conducted to evaluate the possibility that a different schedule of bortezomib, doxorubicin HCl liposome, and dexamethasone might decrease the incidence of peripheral neuropathy yet maintain similar efficacy and allow maintenance of bortezomib dosing for a longer period.

Study identification

NCT ID
NCT00366106
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
32 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2006
Primary completion
Feb 28, 2011
Completion
Feb 28, 2011
Last update posted
Apr 5, 2012

2006 – 2011

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Wilshire Oncology Medical Group, Inc. La Verne California 91750
Medical Oncology & Hematology Waterbury Connecticut 06708
Advanced Medical Specialties Miami Florida 33176
Northeast Georgia Cancer Care Athens Georgia 30607
Augusta Oncology Associates, PC Augusta Georgia 30901
Northwest Georgia Oncology Centers, PC Marietta Georgia 30060
North Idaho Cancer Center Coeur d'Alene Idaho 83814
Oncology-Hematology Associates, P.A. Clinton Maryland 20735
Hematology Oncology Centers of the Northern Rockies, PC Billings Montana 59101
Arena Oncology Associates Lake Success New York 11042
Tri-County Hematology and Oncology Associates Canton Ohio 44718
Mid Ohio Oncology/Hematology, Inc. Columbus Ohio 43215
Lancaster Cancer Center, Ltd. Lancaster Pennsylvania 17605
The West Clinic Memphis Tennessee 38120
Cancer Specialists of Tidewater, Ltd. Chesapeake Virginia 23320

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00366106, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 5, 2012 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00366106 live on ClinicalTrials.gov.

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