Review how data-driven approaches, including physiologically based pharmacokinetic (PBPK) modeling, parallel formulation screening, API sparing techniques, and optimal early dosing strategies can help avoid development pitfalls for small-molecule drug candidates on the path to clinic. Live: Wednesday, Sept. 23, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after final airing until Sept. 23, 2021
Register free: https://www.pharmtech.com/pt_w/strategies_to_accelerate
Event Overview:
Development of orally administered small molecules is becoming more challenging as an increasing number of molecules in pipelines are exhibiting a trend toward higher lipophilicity and molecular weight, which can lead to poor solubility and bioavailability.
During this webcast, industry experts will introduce a fast and efficient development process that can help deliver the right clinical candidate, best formulation strategy, and an optimal dosage form to Phase 1. The presentation will also review details of some established data-driven approaches, including physiologically based pharmacokinetic (PBPK) modeling, parallel formulation screening, API sparing techniques, and optimal early dosing strategies that will help avoid development pitfalls and de-risk a molecule’s path to clinic.
Key Learning Objectives:
Speakers:
Katarina Vulic, Principal Scientist, Novartis Institutes for BioMedical Research
Lisa Caralli, Science and Technology Director, Pharmaceutics at Catalent Pharma Solutions
Time and Date: Wednesday, Sept. 23, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST
On demand available after final airing until Sept. 23, 2021
Sponsor: Catalent
Register free: https://www.pharmtech.com/pt_w/strategies_to_accelerate