drugset / Trial / NCT04230148

Study of Safety, Tolerability and Clinical Outcomes of Egaten in Fascioliasis Patients (6 Years of Age or Older).

NCT04230148 ↗

Phase 4 Completed 301 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The study evaluated safety and tolerability along with clinical outcomes of Egaten administered as per the FDA approved dosing regimen of 2 doses of 10 mg/kg (given approximately 12 hours apart) in Fascioliasis participants (≥ 6 years of age).

Timeline

Start
2022-02-11
Primary completion
2026-03-27
Completion
2026-03-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Triclabendazole Small molecule 10 mg/kg Oral

Indications