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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.
Principal Investigator | Dynio Honrubia, MD |
Type of Trial | Prospective/Interventional |