Speakers:
- Patricia Bradford, Antimicrobial Development Specialists LLC (USA)
- Alita Miller, Entasis Therapeutics (USA)
Moderator: Michael Mourez, École d’Ingénieurs de PURPAN (France)
Presentations:
Screen to pre-clinical candidate (Alita Miller):
- Discovery strategies
- Hit-to-lead generation
- MOA studies
- Spectrum of activity
- Resistance studies
- In vitro toxicity assessments
- PK/PD characterization
Pre-clinical candidate to phase 1 (Patricia Bradford):
- Non-clinical package requirements for first-in-human studies
- Dose selection
- Non-clinical toxicity
- CMC considerations
- Regulatory process/pathways
The presentations were followed by a Q&A session.
This live webinar including interactive Q&A session was broadcast on 25 February 2021.
If you have questions or comments, please let us know: revive@gardp.org.