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Clinical Trial Summary

A multicentre, prospective, open label study of acromegalic patients evaluating the efficacy and safety of different dose-intervals of Lanreotide Autogel 120mg according to international standards and compared to previous treatment with Octreotide LAR 10, 20 or 30 mg.


Clinical Trial Description

Six repeated applications of Lanreotide Autogel 120mg administered every 28, 42 or 56 days. For the first three injections, the interval depends on the Octreotide LAR dosage administered previously. The dose interval is titrated after injection 3 depending on the efficacy of the therapy with Lanreotide Autogel ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00444873
Study type Interventional
Source Ipsen
Contact
Status Completed
Phase Phase 3
Start date January 2005
Completion date January 2008

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