drugset / Trial / NCT06528457

Study to Examine the Effects of Oral Fenretinide

NCT06528457

Phase 2 Completed 15 enrolled Island Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

This randomized, placebo controlled single center study examines the extent to which 600 mg/m2/day of orally administered ISLA101 (fenretinide), given prophylactically or therapeutically, may reduce or eliminate signs and symptoms of dengue virus (DENV) infection over 29 days following subcutaneous challenge of healthy subjects with 'Dengue 1 Live Virus Human Challenge' (DENV-1-LVHC). Humoral and cellular immune responses, both innate and adaptive, circulating virus, and changes in clinical laboratory measures will also be examined.

Timeline

Start
2024-09-05
Primary completion
2025-05-21
Completion
2025-07-21

Drugs

EvaluationDrugModalityDoseRoute
Subject fenretinide Small molecule 300 mg/m2 Oral

Indications