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Clinical Trial Summary

Liprotamase consists of 3 soluble, non-porcine digestive enzymes, lipase, protease, and amylase, combined in a fixed ratio. Liprotamase is stable in the stomach and can be formulated without enteric coating for administration either as a capsule or as a dosing solution dissolved in water or juice.


Clinical Trial Description

The purpose of the present study is to evaluate the safety of long-term use of liprotamase in the management of cystic fibrosis-related exocrine pancreatic insufficiency ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02823964
Study type Interventional
Source Anthera Pharmaceuticals
Contact
Status Completed
Phase Phase 4
Start date September 2016
Completion date March 2018

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