Last updated on January 2020

A Study to Evaluate the Safety and Efficacy of MEDI8897 for the Prevention of Medically Attended RSV LRTI in Healthy Late Preterm and Term Infants

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Respiratory syncytial virus infection
  • Age: - 1 Years
  • Gender: Male or Female

Key Inclusion Criteria:

  • Healthy infants in their first year of life and born at or after 35 weeks 0 days GA
  • Infants who are entering their first RSV season at the time of screening

Key Exclusion Criteria:

  • Meets national or other local criteria to receive commercial palivizumab
  • Any fever ( 100.4F [ 38.0C], regardless of route) or acute illness within 7 days prior to randomization
  • Active RSV infection (a child with signs/symptoms of respiratory infection must have negative RSV testing) or known prior history of RSV infection
  • Receipt of palivizumab or other RSV monoclonal antibody or any RSV vaccine, including maternal RSV vaccination

Recruitment Status: Open

Brief Description Eligibility Contact Research Team

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