Defining Your First In-Patient Study Dose to Optimize Safety & Efficacy

Time: 11:30 am
day: Day 2 Track B AM

Details:

  • Implementing a suitable dose-ranging study using appropriate preclinical scaling methods; PK and pharmacodynamic correlations
  • Exploring how to determine dose parameters
  • How accurate are our approaches for predicting human FIH doses?
  • Key immunogenicity variables for systemic vs local administration and the resulting dosing implications

Speakers: