Trial intelligence / Profile preview

HRS-3095 in Healthy Subjects

NCT07230418Phase 1Completed

Sponsor
Chengdu Suncadia Pharmaceuticals
Start
Nov 2025
Primary completion
Apr 2026
Modality
Small Molecules
Countries
1
01

Overview

Phase 1, randomised, double-blind trial in chronic spontaneous urticaria (CSU) comparing HRS-3095 Group with HRS-3095 Placebo Group (2 arms). Primary endpoints: Incidence of adverse events at 21 days and Incidence of serious adverse events at 21 days. Started Nov 2025; status: completed.

02

Drugs

HRS-3095
03

Conditions

chronic spontaneous urticaria (CSU)

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