Evaluating Phase II/III Efficacy & Safety Insights from an ADC in EGFR-Mutated NSCLC

12:00 pm - Monday 8th March 2027

  • Reviewing combined phase II and III efficacy and safety data supporting accelerated approval of the ADC in EGFR-mutated NSCLC
  • Exploring key learnings on toxicity management and therapeutic index optimisation drawn from early-phase through late-phase development of the program
  • Outlining key safety parameters to take forward in late-stage trials

Speakers:

Senior Medical Director, Global Oncology Clinical Development
Daiichi Sankyo