Join this educational webinar to hear three specialists share their expertise on how sponsors can optimize their DDI evaluation process, spanning from preclinical to clinical.
TORONTO (PRWEB)
November 20, 2020
What sponsors always wanted to know about DDI waivers, cocktails and modeling, but were afraid to ask.
As today’s patients are prescribed an increasing number of medications, drug development sponsors must be aware of potential drug-drug interactions (DDIs) for their product in order to avoid unexpected pharmacological effects and to provide accurate labeling.
Join this educational webinar to hear three specialists share their expertise on how sponsors can optimize their DDI evaluation process, spanning from preclinical to clinical.
The first part of this webinar will provide an overview of in vitro DDI assays and the use of physiologically-based pharmacokinetic (PBPK) modeling to help interpret results, support waivers and focus on interactions with clinical DDI risk, before moving into study design considerations to ensure robust and efficient assessment. Population pharmacokinetics (PopPK) strategies will then be presented to explain how modeling and simulation can help evaluate DDI risk and support labeling.
Join experts from Covance, Dan Albaugh, MS, Associate Director, Global Metabolism and Environmental Sciences; Andreas M. Reichl, MD, Scientific Director, Clinical Pharmacology, Medical and Scientific Affairs; and Brandon Gufford, PharmD, PhD, Senior Pharmacokineticist, Clinical Pharmacology Services, in a live webinar on Monday, December 7, 2020 at 10am EST (3pm GMT/UK).
For more information, or to register for this event, visit Strategies to Optimize Your Drug-Drug Interaction Program.
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