Study of Oral LBH589 in Adult Participants With Refractory/Resistant Cutaneous T-Cell Lymphoma (CTCL)

PHASE2TerminatedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

July 5, 2007

Primary Completion Date

September 30, 2009

Study Completion Date

September 22, 2009

Conditions
Cutaneous T-Cell Lymphoma
Interventions
DRUG

Panobinostat

Panobinostat, 20 mg, hard gelatin capsules, orally, thrice weekly.

Trial Locations (18)

10016

NYU Clinical Cancer Center, New York

10466

Our Lady of Mercy Medical Center/Comprehensive Cancer Center, The Bronx

14263

Roswell Park Cancer Institute, Buffalo

15213

University of Pittsburg Medical Center, Pittsburgh

27157

Wake University Health Sciences, Winston-Salem

30912

Medical College of Georgia, Augusta

33136

Florida Academic Dermatology Centers, Miami

35233

University of Alabama at Birmingham/ The Kirklin Clinic, Birmingham

38138

The Jones Clinic, Germantown

60612

Rush Presbyterian Hospital/St. Luke's Medical Center, Chicago

63110

St. Louis University Cancer Cennter, St Louis

68198

Nebraska Medical Center, Omaha

74104

University of Oklahoma-Tulsa, Tulsa

77030

MD Anderson Cancer Center/University of Texas, Houston

80010

University of Colorado Health Sciences Center/Anschutz Cancer Pavillion, Aurora

90095

UCLA Medical Center School of Medicine/ Dpt of Hematology-Oncology, Los Angeles

97239

Craig Okada, Portland

98109-102

Seattle Cancer Care Alliance, Seattle

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY