Bringing a small molecule from discovery to a viable drug product requires overcoming significant challenges—from selecting the right candidate to ensuring optimal formulation. This seminar will explore key strategies to improve clinical success and leverage cutting-edge formulation technologies like Hot Melt Extrusion (HME) to enhance bioavailability. Join us for an insightful discussion led by industry experts, with opportunities for networking and Q&A.
Location:
Life Sciences Pennsylvania
411 Swedeland Road
Suite 23-1080
King of Prussia, PA 19406
Date and time: Thursday, April 24th 2025 at 11AM-3PM EST
Speakers:
Samuel S. Chuang, PhD
Senior Director, Scientific Advisory Services, Charles River Laboratories
With over 25 years in drug development spanning academia, biotech, and preclinical CROs, Sam specializes in regulatory strategy and toxicology. He has led global scientific teams, supported IND/CTA submissions, and advised on discovery and safety packages across various drug classes and therapeutic areas. Sam holds a Ph.D. in Microbiology and Immunology from the University of Tennessee-Memphis and has authored numerous scientific publications, abstracts, and a patent.
Hibreniguss Terefe, PhD
Director, Product Development, Ardena Somerset, NJ
With over 27 years in pharmaceutical R&D and manufacturing, Hibreniguss specializes in preclinical and clinical solid oral dosage form development. His expertise includes solubility enhancement, modified-release formulations, and twin-screw extrusion. He previously held leadership roles at Catalent Pharma Solutions and ExxPharma Therapeutics. He earned his Ph.D. in Pharmaceutical Chemistry and a Pharmacy degree from Westfälische Wilhelms-Universität Münster, Germany, and was a Fulbright Visiting Scholar at UC Berkeley.
Secure your free registration now.
Limited seats available.
Presenter: Samuel S. Chuang, PhD
Senior Director, Scientific Advisory Services, Charles River Laboratories
Session Overview:
Early-stage drug development is complex, and hasty decision-making in hit-to-lead and lead optimization can lead to costly failures. This session will cover key strategies to refine your approach and improve clinical success:
Enhancing candidate selection in early drug discovery
Leveraging in vivo pharmacology for proof-of-concept data
Strengthening IND strategies for a smoother regulatory path
Optimizing CRO partnerships for efficiency and success
Presenter: Hibreniguss Terefe, PhD
Director, Product Development, Ardena Somerset, NJ
Session Overview:
Hot Melt Extrusion (HME) is a powerful technology for addressing solubility and bioavailability challenges in drug development. This session will highlight:
Improved bioavailability and product stability
Accelerated development timelines
Cost-effective and scalable manufacturing
Versatile formulation capabilities
An open forum to ask questions and gain deeper insights from our experts.
A chance to connect with peers, explore collaborations, and hold 1:1 meetings.