2023 ACCP Virtual Journal Club Webinar-August | Impact of Multiple Concomitant CYP3A Inhibitors on Venetoclax Pharmacokinetics: A PBPK and Population PK-Informed Analysis | ON DEMAND
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2023 ACCP Virtual Journal Club Webinar: Impact of Multiple Concomitant CYP3A Inhibitors on Venetoclax Pharmacokinetics: A PBPK and Population PK-Informed Analysis | ON DEMAND
On Demand webinar recording: August 16th, 2023 to August 16th, 2026
Why is this article important to your practice?
Venetoclax is an approved BCL-2 inhibitor that is primarily metabolized by cytochrome P450 3A (CYP3A). Although venetoclax exposure has been well characterized with one concomitant CYP3A inhibitor, complex drug-drug interactions involving more than one inhibitor have not been systematically evaluated despite the common polypharmacy in the target populations. In this webinar, the author will leverage physiologically-based pharmacokinetic (PBPK) and population pharmacokinetic (PK) modeling to describe the potential impact of multiple concomitant CYP3A inhibitors on venetoclax pharmacokinetics. The modeling approaches were informed by clinical data in the presence of single or multiple CYP3A inhibitors and the effects of one or more inhibitors were systematically evaluated within these modeling frameworks. Learners that complete this activity will be able to describe the potential impact of multiple concomitant CYP3A inhibitors on venetoclax pharmacokinetics using PBPK and population PK modeling.
Target Audience:
Physicians, Pharmacists, PhDs and other healthcare professionals interested in PBPK/PopPK modeling, drug-drug interactions.
Learning Objectives
After completing this activity, the learner will be able to:
- Describe the rationale to assess and quantify the potential impact of multiple concomitant CYP3A inhibitors on venetoclax pharmacokinetics;
- Describe the approaches and validation procedures used to inform dose adjustment for co-administration of venetoclax with multiple CYP3A inhibitors;
- Describe the benefits and limitations of these approaches to identify the potential impact of multiple concomitant medications in the development of new agents.
Ahmed Salem, PhD
Senior Research Fellow/Senior Director of Clinical Pharmacology & Pharmacometrics
AbbVie, Inc
Ahmed Salem, PhD, FCP is a Senior Research Fellow/Senior Director of Clinical Pharmacology and Pharmacometrics at Abbvie and an adjunct Professor at University of Minnesota. Dr. Salem is a pharmacist and got his PhD in 2010 from the University of Minnesota with a focus on Pharmacometrics and a minor in Biostatistics. In his industry role, Dr. Salem contributed to 15 different FDA and EMA approvals of new drugs, dosage forms or dosage regimens. He has over 230 publications with an i-10 index of 150 and H index of 45 and holds 10 patents in the US and EU. He has worked on over 200 Phase I, II and III clinical trials. Dr Salem is the recipient of the ACCP Tanabe Investigator Award. He was also the recipient of the AAPS High Impact Article Award in addition to other awards and recognition from the IQ-Clinical Pharmacology Leadership Group (CPLG), UMN and AbbVie. He was also selected as a Fellow of ACCP and as a Senior Research Fellow of the Abbvie Community of Science. Dr. Salem has been an invited speaker and chair at multiple conferences such as ACoP, ASCPT, ACCP, FDA workshops.
