Long-term Safety and Efficacy Study of Octreotide Implant in Patients With Acromegaly



Status:Archived
Conditions:Skin Cancer, Endocrine
Therapuetic Areas:Endocrinology, Oncology
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:February 2011
End Date:April 2013

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Trial Summary
Trial Overview
Inclusion Criteria

PHASE IIIB, OPEN-LABEL, MULTICENTER STUDY TO EVALUATE THE LONG-TERM SAFETY AND EFFICACY OF AN 84-MG OCTREOTIDE SUBCUTANEOUS HYDROGEL IMPLANT IN SUBJECTS WITH ACROMEGALY


This is a long term study to evaluate the safety, tolerability and efficacy of an Octreotide
Implant in patients that were previously treated with an Octreotide implant.


Evaluation on the long-term safety and tolerability, including local tolerability of the
implant site, of the 84-mg octreotide hydrogel implant in subjects with acromegaly who had
been successfully treated with the 84-mg octreotide hydrogel implant in the Phase III study
IP107-001.


We found this trial at
6
sites
Clinical Trial Facility
Denver, Colorado
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Clinical Trial Facility
Centralia, Illinois
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Centralia, IL
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Clinical Trial Facility
Chevy Chase, Maryland 20815
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Chevy Chase, MD
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Clinical Trial Facility
Lima, Ohio
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Lima, OH
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Clinical Trial Facility
Medford, Oregon
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Medford, OR
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Clinical Trial Facility
Mountlake Terrace, Washington
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Mountlake Terrace, WA
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