Panel Discussion: Harnessing MRD to Inform Clinical Trial Decision Making & Improve Dosage Regimes
Time: 3:30 pm
day: Day One Track B (1)
Details:
- How to integrate MRD into clinical trial designs to tailor dosage regimes more precisely
- Leveraging MRD insights to refine dosage escalation and de-escalation protocols for optimal efficacy and safety
- How to use MRD data to adjust treatment strategies and inform Standard of Care protocols
