Clinical Trial

D5290C00004 – A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of MEDI8897, a Monoclonal Antibody With an Extended Half-life Against Respiratory Syncytial Virus, in Healthy Late Preterm and Term Infants (MELODY)

Study Status:

Contact Information:

Please contact us for more information or to learn if you are eligible to participate.

Study Purpose

This study aims to assess the efficacy of MEDI8897 when administered as a single fixed IM dose to infants ≥ 35 weeks 0 days GA and entering their first RSV season, in reducing medically attended LRTI due to RT-PCRconfirmed RSV, compared to placebo.

Information

Principal Investigator Dynio Honrubia, MD
Co-PI
Sponsor
Type of Trial Prospective/Interventional