Oral Drug Product Delivery at Quotient Sciences

Leveraging Real-Time Clinical Data to Deliver Certainty in Solubility Enhancement and Modified Release Development

12 December 2024
Overview

Drug product optimization is a critical development step that is common for most drugs that are progressing through today’s development pipelines to respond to suboptimal exposure profiles, to transition from an early development formulation to one suitable for chronic administration in patients, or as part of a life-cycle management strategy.

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Traditional drug product optimization processes take 12-18 months to complete and place significant emphasis on the predictive power of laboratory and preclinical assessments. This approach is a non-optimal working model necessitated by the multiple disciplines required to develop, make and test new formulations in humans.

In this presentation, John McDermott and Andrew Parker will describe how the application of Quotient Sciences’ Translational Pharmaceutics® to re-engineer this process has created a Rapid Formulation Development and Clinical Testing approach, using clinical data to improve decision-making and halve development timelines using case studies from over 300 delivered programs.

Key learning objectives:

  • Develop an understanding of Translational Pharmaceutics®
  • Hear how Translational Pharmaceutics® can be applied to rapidly develop new formulations and evaluate their clinical performance
  • Hear case studies in spray drying, lipid formulation development and modified release

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Times

Thursday 12th December, 2024
3pm BST/ 4pm CET

Meet our experts:

John McDermott

Vice President, Scientific Consulting

John McDermott is Vice President of Scientific Consulting at Quotient Sciences. John leads Quotient Sciences' global drug developm...

About John
Dr. Andrew Parker

Senior Drug Development Consultant

Dr. Andrew Parker has two decades of experience in the pharmaceutical industry, spanning from preclinical development, through ear...

About Andrew

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