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Completed Phase 2 Interventional Results available

Efficacy of Panobinostat in Patients With Relapsed and Bortezomib-refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT01083602

Public ClinicalTrials.gov record NCT01083602. 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 10, 2026, 6:19 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, Multi-center, Single Arm, Open Label Study of Panobinostat in Combination With Bortezomib and Dexamethasone in Patients With Relapsed and Bortezomib-refractory Multiple Myeloma

Brief summary

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

This study is designed to assess the effectiveness of the combination of Panobinostat plus Bortezomib and Dexamethasone in patients with relapsed and bortezomib refractory Multiple Myeloma.

Study identification

NCT ID
NCT01083602
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
55 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
May 31, 2010
Primary completion
Jan 31, 2014
Completion
Jan 31, 2014
Last update posted
Dec 20, 2017

2010 – 2014

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
University of California at Los Angeles Los Angeles California 90095
Stanford University Medical Center Division of Hematology Stanford California 94305-5826
H. Lee Moffitt Cancer Center & Research Institute Tampa Florida 33612
Emory University School of Medicine/Winship Cancer Institute Dept. of Winship Cancer Inst. Atlanta Georgia 30322
Georgia Regents University MedCollege of GA Cancer Ctr 2 Augusta Georgia 30912
Hematology/Oncology of the North Shore Orchard Healthcare Res. Inc. Skokie Illinois 60076
Dana Farber Cancer Institute Boston Massachusetts 02115
Somerset Hematology Oncology Associates Somerset Hema Oncol Assoc (2) Somerset New Jersey 08873
Montefiore Medical Center The Bronx New York 10467
Duke University Medical Center Dept. of DUMC (4) Durham North Carolina 27710
Vanderbilt University Medical Center, Clinical Trials Center Vanderbilt UMC Nashville Tennessee 37212
MD Anderson Cancer Center/University of Texas MD Anderson CC Houston Texas 77030
Medical College of Wisconsin Milwaukee Wisconsin 53226

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 NCT01083602, 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 Dec 20, 2017 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01083602 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →