drugset / Trial / NCT04184895

A Study to Assess the Safety, Tolerability and Immunological Response of ASP2390 in Adult Subjects Allergic to House Dust Mites

NCT04184895 ↗

Phase 1 Active not recruiting 28 enrolled Astellas Pharma Global Development, Inc.
RandomizedSequentialDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of multiple ascending intradermal doses of ASP2390 in adult male and female participants allergic to house dust mites (HDM). This study will also evaluate the effect of multiple ascending intradermal doses of ASP2390 on HDM-specific immunoglobulin G subclass 4 (IgG4) levels in adult male and female participants allergic to HDM.

Timeline

Start
2020-09-09
Primary completion
2022-12-22
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject ASP2390 Unknown — Other