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Clinical trial

A Phase II, Multicenter, Parallel-Group, Active-Controlled, Randomized, Double-blind, Dose-Ranging Study to Evaluate the Efficacy and Safety of Different Doses of Creon IR in Subjects With Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis

NCT02415959 is registered in ClinicalTrials.gov with Abbott as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase II, Multicenter, Parallel-Group, Active-Controlled, Randomized, Double-blind, Dose-Ranging Study to Evaluate the Efficacy and Safety of Different Doses of Creon IR in Subjects With Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis
Lead sponsor
Abbott
Phase
Phase 2
Overall status
Completed
Start date
March 31, 2015
Completion date
July 31, 2015
Enrollment
70 (actual)
Sites
17

Conditions

As the registry lists them; a condition with its own page is linked.

exocrine pancreatic insufficiency in subjects with cystic fibrosis