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Spots Global Cancer Trial Database for Study of Human Monoclonal Antibody to Treat Mycosis Fungoides and Sezary Syndrome

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Trial Identification

Brief Title: Study of Human Monoclonal Antibody to Treat Mycosis Fungoides and Sezary Syndrome

Official Title: Open Label, Dose Escalation, Followed by Open Label,Single Arm Clinical Trial of HuMax-CD4 in Patients With Mycosis Fungoides Type CTCL (Stage IB-IVB) or Sezary Syndrome Who Are Refractory or Intolerant to Targretin® (Bexarotene) and One Other Standard Therapy

Study ID: NCT00127881

Study Description

Brief Summary: The purpose of this study is to determine the efficacy of the drug, HuMax-CD4, in patients with mycosis fungoides(MF) and sezary syndrome who are intolerant to or do not respond to treatment with Targretin® and one other standard therapy.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama at Birmingham, Birmingham, Alabama, United States

Stanford University Medical Center, Stanford, California, United States

University of Colorado, Aurora, Colorado, United States

H. Lee Moffitt Cancer Center, Tampa, Florida, United States

The Emory Clinic, Atlanta, Georgia, United States

Northwestern University, Chicago, Illinois, United States

Tulane University Health Science Center, New Orleans, Louisiana, United States

Boston Medical Center, Boston, Massachusetts, United States

University of Michigan Medical Center, Ann Arbor, Michigan, United States

Memorial Sloan Kettering, New York City, New York, United States

New York Medical Center, New York, New York, United States

SUNY Upstate Medical University, Syracuse, New York, United States

Duke University Medical Center, Durham, North Carolina, United States

University Hospital of Cleveland, Cleveland, Ohio, United States

Ohio State University, Columbus, Ohio, United States

Oregon Health & Science University, Portland, Oregon, United States

University of Pennsylvania Health System, Philadelphia, Pennsylvania, United States

Middle Tennessee Research Institute, Nashville, Tennessee, United States

MD Anderson Cancer Center, Houston, Texas, United States

Hopital de I'Hotel-Dieu, Lyon Cedex 02, , France

Consultation Dermatologie Niveau moins 1 Hopital Archet 2, Nice, , France

Hopital Saint-Louis Service de Dermatologie, Paris Cedex 10, , France

Centre Hospitalier Lyon Sud Bat. 1F 1er etage service Hematologie, Pierre Benite Cedex, , France

Skin Cancer Center Charite Mitte Dermatologie Fran Ramona Kursawa, Berlin, , Germany

University of Essen - Universitatsklinikum Essen z. Hd. Frau Desire Zieling, Essen, , Germany

University of kiel, Klinik Fur Dermotologie, Christian-Albrechts-Universitat Zu, Kiel, , Germany

Klinikum Minden / Hautklinik Minden, Minden, , Germany

University of Wurzburg - Universitatsklinikum Wurzburg dermato-onkologische studien, Wurzburg, , Germany

Instituto di Ematologia e Oncologia Medica "L. & A. Seragnoli", Bologna, , Italy

Day Hospital Oncologico-Presidio Ospedaliero Firenze Centro Ospedale Santa Maria Nuova Azienda Sanitaria di Firenze, University of Florence, Florence, , Italy

University of Milan-Fondazione IRCCS di Natura Pubblica Ospedale Maggiore Policlinico Mangiagalli e Regina Elena di Milano via Francesco Sforza, Milan, , Italy

Instituto Dermopatico dell'Immacolata IRCCS via Monti di Creta, Roma, , Italy

University of Turin SCDU Dermosifilopatia 2 A.S.O. Molinette S.Giovanni Battista, Turin, , Italy

Hospital Universitario de la Princesa, Madrid, , Spain

Maternidad Planta Baja, Hospital 12 de Octubre, Madrid, , Spain

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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