Trial intelligence / Profile preview

YKYY025 in Healthy Adult Participants

NCT07694557Phase 1Recruiting

Sponsor
Yuekang Pharmaceutical
Start
Jul 2026
Primary completion
Jul 2028
Countries
1
01

Overview

Phase 1, randomised, double-blind trial in respiratory syncytial virus infection (RSV) comparing YKYY025 group with YKYY025 Placebo group (2 arms). Primary endpoints: Adverse Events at 30 days, Serious Adverse Events at 12 months and 4 more. Started Jul 2026; status: recruiting.

02

Drugs

YKYY025
03

Conditions

respiratory syncytial virus infection (RSV)

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