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Safety and Biological Activity of C2L-OCT-01 PR in Acromegalic Patients

Acromegaly Clinical Trial

Official title:
Safety and Biological Activity of a New Prolonged Release Formulation of Octreotide Acetate, C2l-OCT-01 PR, Administered Intra Muscularly Every 4, 5 or 6 Weeks in Acromegalic Patients

Clinical Trial Summary

The purpose of this study is to assess the safety profile of a new prolonged release formulation of octreotide acetate, C2L-OCT-01 PR, administered intra muscularly every 4, 5 or 6 weeks in acromegalic patients.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00642421
Study type Interventional
Source Ambrilia Biopharma, Inc.
Contact
Status Terminated
Phase Phase 3
Start date February 2008
Completion date August 2009
View Details
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