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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 Oct 18, 2026, 1:25 PM 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
Jul 2006 (Type not available)
Primary completion
Mar 2011 (Actual)
Completion
Mar 2011 (Actual)
Last update posted
Apr 6, 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 6, 2012 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00366106 live on ClinicalTrials.gov.

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