OPTION: A Trial to Assess the Safety & Efficacy of MS1819 in Patients With Exocrine Pancreatic Insufficiency Due to Cystic Fibrosis
Completed · Phase 2
Conditions studied: Exocrine Pancreatic Insufficiency (EPI), Cystic Fibrosis (CF)
In brief
The primary objectives of this study are to assess the safety and efficacy of MS1819-SD vs porcine pancreatic enzyme replacement therapy (PERT) in patients with exocrine pancreatic insufficiency (EPI) due to cystic fibrosis (CF).
Key facts
- Study ID
- NCT03746483
- Run by
- Entero Therapeutics
- People needed
- 41
- Starts
- 2019-01-10
- Expected to finish
- 2019-07-27
- Last updated by the study team
- 2022-06-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Cystic fibrosis, based on 2 clinical features consistent with CF, plus initial diagnostic sweat chloride ≥ 60 mmol/L
- Under stable dose of porcine PERT
- A fair or better nutritional status
- Fecal elastase <100 µg/g
- Standard-of-care medications including Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) modulators are allowed
You may not qualify if…
- History or diagnosis of fibrosing colonopathy
- Any chronic diarrheal illness unrelated to pancreatic insufficiency
- Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) level ≥5 ×upper limit of normal (ULN), or total bilirubin level ≥1.5 ×ULN at the Screening visit
- Feeding via an enteral tube during 6 months before screening
- Forced expiratory volume ≤30% at the Screening visit
Where it is running
- Investigator Site 105 — Long Beach, California, United States
- Investigator Site 102 — Altamonte Springs, Florida, United States
- Investigator Site 107 — Miami, Florida, United States
- Investigator Site 101 — Glenview, Illinois, United States
- Investigator Site 111 — Wichita, Kansas, United States
- Investigator Site 108 — Portland, Maine, United States
- Investigator Site 103 — Las Vegas, Nevada, United States
- Investigator Site 110 — Cleveland, Ohio, United States
- Investigator Site 104 — Toledo, Ohio, United States
- Investigator Site 106 — Hershey, Pennsylvania, United States
- Investigator Site 109 — Dallas, Texas, United States
- Investigator Site 203 — Karpacz, Poland
- Investigator Site 202 — Rabka-Zdrój, Poland
- Investigator Site 204 — Sopot, Poland
Full record on ClinicalTrials.gov
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