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Terminated Phase 2 Interventional Results available

Efficacy and Safety of LBH589B in Adult Patients With Multiple Myeloma

ClinicalTrials.gov ID: NCT00445068

Public ClinicalTrials.gov record NCT00445068. 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 Jul 22, 2026, 4:04 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 Study Of Oral LBH589 In Adult Patients With Multiple Myeloma Who Have Received At Least Two Prior Lines Of Therapy And Whose Disease Is Refractory To The Most Recent Line Of Therapy

Study identification

NCT ID
NCT00445068
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
38 participants

Conditions and interventions

Interventions

  • LBH589 Drug

Drug

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
Apr 15, 2007
Primary completion
May 18, 2008
Completion
Dec 24, 2009
Last update posted
Jul 13, 2021

2007 – 2009

United States locations

U.S. sites
24
U.S. states
17
U.S. cities
22
Facility City State ZIP Site status
Mayo Clinic Scottsdale Arizona 85259
Aptium Oncology Berkeley California 94704
City of Hope Duarte California 91010
UCSF San Francisco California 94143
Stanford Stanford California 94305
Rocky Mountain Cancer Center Denver Colorado 80218
Christiana Care Newark Delaware 19718
Moffitt Cancer Center Tampa Florida 33612
Emory University Atlanta Georgia 30322
Rush University Chicago Illinois 60612
University of Chicago Chicago Illinois 60637
Indiana University Indianapolis Indiana 46203
University of Iowa Iowa City Iowa 52240-1515
Dana Farber Boston Massachusetts 02115
University of Michigan Ann Arbor Michigan 48109
Washington University St Louis Missouri 63110
Hackensack University Hackensack New Jersey 07456
Duke Durham North Carolina 27710
Wake Forest Winston-Salem North Carolina 27157
Metrohealth Cleveland Ohio 44109
Sarah Canon Research Center Nashville Tennessee 37203
Vanderbilt Nashville Tennessee 37212
University of Texas Southwestern Dallas Texas 75390-9179
CTRC San Antonio Texas 78258

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00445068, 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 Jul 13, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00445068 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →