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Spots Global Cancer Trial Database for Long Term Safety and Efficacy of Pasireotide s.c. in Patients With Cushing's Disease

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Trial Identification

Brief Title: Long Term Safety and Efficacy of Pasireotide s.c. in Patients With Cushing's Disease

Official Title: Non-interventional Study for the Generation of Long Term Safety and Efficacy Data of Pasireotide s.c. in Patients With Cushing's Disease (Post-Authorization Safety Study)

Study ID: NCT02310269

Interventions

SOM230

Study Description

Brief Summary: This is a non-interventional, multinational, multi-center post-marketing study, to further document the safety and efficacy of pasireotide s.c. administered in routine clinical practice in patients with Cushing's disease. Patients with Cushing's disease and treated with pasireotide s.c. alone and in combination with other therapies will be monitored. For this study, each enrolled patient will be followed up for 3 years after enrollment. Patients who permanently discontinue pasireotide s.c. prior to completing the 3-year observation period will be followed up for 3 months after the last dose of pasireotide s.c.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

St Josephs Hospital and Medical Center, Phoenix, Arizona, United States

University of Southern California CSOM230B2410 - SC, Los Angeles, California, United States

Massachusetts General Hospital SC - SOM230B2410, Boston, Massachusetts, United States

Ohio State University SC - SOM230B2410, Columbus, Ohio, United States

Endocrinology Services, Bend, Oregon, United States

Allegheny Endocrinology Associates, Pittsburgh, Pennsylvania, United States

Swedish Medical Center Dept.ofSeattle Neuroscience(2), Seattle, Washington, United States

Recordati Investigative Site, Montreal, Quebec, Canada

Recordati Investigative Site, Sherbrooke, Quebec, Canada

Recordati Investigative Site, Quebec, , Canada

Recordati Investigative Site, Cali, , Colombia

Recordati Investigative Site, Amiens Cedex 1, , France

Recordati Investigative Site, Bron Cedex, , France

Recordati Investigative Site, Lille Cedex, , France

Recordati Investigative Site, Marseille, , France

Recordati Investigative Site, Montpellier Cedex 5, , France

Recordati Investigative Site, Paris, , France

Recordati Investigative Site, Reims, , France

Recordati Investigative Site, Saint Mande, , France

Recordati Investigative Site, St Priest en Jarez Cedex, , France

Recordati Investigative Site, Aachen, , Germany

Recordati Investigative Site, Berlin, , Germany

Recordati Investigative Site, Duesseldorf, , Germany

Recordati Investigative Site, Erlangen, , Germany

Recordati Investigative Site, Essen, , Germany

Recordati Investigative Site, Freiburg, , Germany

Recordati Investigative Site, Halle, , Germany

Recordati Investigative Site, Hamburg, , Germany

Recordati Investigative Site, Leipzig, , Germany

Recordati Investigative Site, Magdeburg, , Germany

Recordati Investigative Site, Muenchen, , Germany

Recordati Investigative Site, Muenchen, , Germany

Recordati Investigative Site, Oldenburg, , Germany

Recordati Investigative Site, Wuerzburg, , Germany

Recordati Investigative Site, Petach Tikva, , Israel

Recordati Investigative Site, Tel Aviv, , Israel

Recordati Investigative Site, Ancona, AN, Italy

Recordati Investigative Site, Messina, ME, Italy

Recordati Investigative Site, Milano, MI, Italy

Recordati Investigative Site, Milano, MI, Italy

Recordati Investigative Site, Palermo, PA, Italy

Recordati Investigative Site, Padova, PD, Italy

Recordati Investigative Site, Pisa, PI, Italy

Recordati Investigative Site, Torino, TO, Italy

Recordati Investigative Site, Napoli, , Italy

Recordati Investigative Site, Padova, , Italy

Recordati Investigative Site, El Achrafiyé, , Lebanon

Recordati Investigative Site, Maastricht, AZ, Netherlands

Recordati Investigative Site, Nijmegen, , Netherlands

Recordati Investigative Site, Brasov, , Romania

Recordati Investigative Site, Bucuresti, , Romania

Recordati Investigative Site, Cluj, , Romania

Recordati Investigative Site, Târgu-Mureş, , Romania

Recordati Investigative Site, Plymouth, , United Kingdom

Contact Details

Name: Recordati

Affiliation: Recordati Rare Diseases

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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