Overview

Study to Evaluate the Efficacy and Safety of DW1807 in Perennial Allergic Rhinitis Patients With Asthma

Status:
RECRUITING
Trial end date:
2026-09-18
Target enrollment:
Participant gender:
Summary
This study aims to compare the efficacy and safety of DW1807 and DW1807-R2 in patients with perennial allergic rhinitis and comorbid asthma. The primary objective is to demonstrate the superiority of DW1807 over DW1807-R2 in improving the reflective total nasal symptom score (rTNSS) after 4 weeks of treatment.
Phase:
PHASE3
Details
Lead Sponsor:
Daewon Pharmaceutical Co., Ltd.