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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
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:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
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
Name: Recordati
Affiliation: Recordati Rare Diseases
Role: STUDY_DIRECTOR