Leveraging Pilot Study Data, Options for Dosage & Statistics to Achieve Optimum ARDS Clinical Trial Design

Time: 8:00 am
day: Day One

Details:

  • Utilizing data of a pilot study to inform the design of adequate and well controlled studies
  • Reviewing options for dose-ranging in ARDS studies
  • Exploring the statistical implications of treatment benefit in the design of adequate and well-controlled studies

Speakers: