ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study of Oral LBH589 in Adult Patients With Refractory Cutaneous T-Cell Lymphoma

ClinicalTrials.gov ID: NCT00425555

Public ClinicalTrials.gov record NCT00425555. 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 Apr 29, 2026, 9:12 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 Study of Oral LBH589 in Adult Patients With Refractory Cutaneous T-Cell Lymphoma

Study identification

NCT ID
NCT00425555
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
139 participants

Conditions and interventions

Interventions

  • Panobinostat 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
Dec 31, 2006
Primary completion
May 31, 2013
Completion
May 31, 2013
Last update posted
Aug 19, 2021

2007 – 2013

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
University of Alabama at Birmingham/ Kirklin Clinic Kirklin Clinic Birmingham Alabama 35294-0006
City of Hope National Medical Center Duarte California 91010-3000
University of California at Los Angeles Dept. of Hematology-Oncology Los Angeles California 90095
Florida Academic Dermatology Center Miami Florida 33136
Emory University School of Medicine/Winship Cancer Institute Dept. of Hematology (2) Atlanta Georgia 30322
Georgia Health Sciences University Dept.ofMedicalCollegeOfGeorgia Augusta Georgia 30912
NorthwesternUniv.Med.School/Robert H. Lurie Comp.Cancer Ctr Dept. of NorthwesterUMed Chicago Illinois 60611
Indiana University Dept. of IU Cancer Center Indianapolis Indiana 46202
Boston Medical Center StudyCoordinator:CLBH589B2201 Boston Massachusetts 02118
Dana Farber Cancer Institute Deptof DanaFarberCancerInst(3) Boston Massachusetts 02215
University of Michigan Health System Michigan HouseClinTrialsOffice Ann Arbor Michigan 48109
Wake Forest University Baptist Medical Center OutpatientCmprehensivCancerCtr Winston-Salem North Carolina 27157
University Dermatology Consultants Cincinnati Ohio 45219
Oregon Health & Science University Dept. of OHSU Cancer Institute Portland Oregon 97239
University of Pittsburgh Medical Center Department of Dermatology Pittsburgh Pennsylvania 15213
MD Anderson Cancer Center/University of Texas StudyCoordinator:CLBH589B2201 Houston Texas 77030

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 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00425555, 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 Aug 19, 2021 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00425555 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →