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Clinical Trial Summary

Randomized, parallel, active-treatment Phase 1 study of a single dose of orally administered ANG003 with a test meal in adult subjects with cystic fibrosis-related exocrine pancreatic insufficiency. The study's overall objectives are to evaluate the safety, tolerability and effect of four dose levels of ANG003.


Clinical Trial Description

The Phase 1 study was designed to compare a 24h Baseline Substrate Absorption Challenge Test (SACT) period with no enzymes to a 24h ANG003 SACT period with enzymes. Eligible subjects will be randomly assigned with equal allocation to one of four active dose levels of lipase, protease and amylase. Approximately 48 to 60 eligible subjects are planned to be enrolled in the study with 12 to 15 subjects assigned to each dose level from up to 21 investigational sites. ;


Study Design


Related Conditions & MeSH terms

  • Exocrine Pancreatic Insufficiency

NCT number NCT06052293
Study type Interventional
Source Anagram Therapeutics, Inc.
Contact Maria Basco, MD, MPH
Phone 630.863.1761
Email maria.basco@ssistrategy.com
Status Recruiting
Phase Phase 1
Start date August 25, 2023
Completion date June 24, 2024

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