[II-JCKAP4-5] Phase 2 Open-label, Single-arm, Multi-center Clinical Trial of Camostate Mesylate in Patients with Protein-losing Enteropathy after Fontan Operation
Keywords:Camostat mesylate, protein-losing enteropathy, Fontan operation
ObjectiveThis study evaluates the efficacy and safety of Camostat Mesylate in treating protein-losing enteropathy (PLE) in patients post-Fontan operation.MethodsThis phase 2, multicenter, open-label, single-arm trial included patients over 4 years old diagnosed with PLE following a Fontan operation. Camostat Mesylate was added to existing treatments, with follow-up assessments at 1, 3, and 6 months, and a final evaluation one month after discontinuation. Efficacy was measured by changes in serum albumin, stool alpha-1 antitrypsin levels, and PLE symptoms such as diarrhea, edema, weight changes, and ascites.ResultsNineteen patients (average age 17.6 years; 11 males and 8 females) were enrolled. The median time between the Fontan operation and PLE diagnosis was 2.4 years. Eleven patients completed the 6-month follow-up. Serum albumin levels increased from 2.2 to 2.5 g/dL (p=0.461), and stool alpha-1 antitrypsin levels decreased significantly from 266.7 to 44.9 mg/dL (p=0.035). Particularly, patients with diarrhea at baseline showed substantial improvement in both parameters (serum albumin from 2.2 to 2.8, and stool alpha-1 antitrypsin levels from 266.7 to 27.3). No serious adverse events were reported.ConclusionsCamostat Mesylate demonstrated safety and efficacy, increasing serum albumin levels and reducing stool alpha-1 antitrypsin in PLE patients post-Fontan, especially those with diarrhea. Therefore, Camostat Mesylate could be considered as an additional treatment option for patients with PLE following Fontan operation.