Trial intelligence / Profile preview

Safety and Tolerability of EuRSV in Healthy Adults

NCT06216093Phase 1Active, not recruiting

Sponsor
EuBiologics
Start
May 2024
Primary completion
Jul 2025
Modality
Targeted Liposomes, Recombinant Protein Vaccines, Stealth (PEGylated) Liposomes
Countries
1
01

Overview

Phase 1, randomised, double-blind trial of EuRSV in respiratory syncytial virus infection (RSV) (3 arms), sponsored by EuBiologics. Primary endpoints: Occurrence of solicited adverse events at 7 days, Occurrence of immediate adverse events at 30 minutes and 2 more. Started May 2024; status: active, not recruiting.

02

Drugs

EuRSV
03

Conditions

respiratory syncytial virus infection (RSV)

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