drugset / Trial / NCT03051490

RESULT: Reliable, Emergent Solution Using Liprotamase Treatment

NCT03051490 ↗

Phase 3 Unknown 140 enrolled Anthera Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

Liprotamase powder is a non-porcine, soluble and stable mixture of biotechnology-derived lipase, protease, and amylase digestive enzymes. The purpose of the present study is to to evaluate the non-inferiority of liprotamase compared with porcine-derived, enterically-coated pancreatic enzyme replacement therapy (PERT). The primary efficacy endpoint of the study will be comparative efficacy measured as the change from baseline in the coefficient of fat absorption (CFA) in Cystic Fibrosis patients with exocrine pancreatic insufficiency (EPI).

Timeline

Start
2017-04-28
Primary completion
2018-02-28
Completion
2018-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Liprotamase Protein / enzyme biologic — Oral
Comparator Porcine PERT Protein / enzyme biologic — Oral