Designing Better Drug Candidates

Only about 4% of candidate drugs reach the market. The main culprits of this failure are due to issues with dosing , exposure and toxicity. Join us as Dr. Paul Leeson shares how improving candidate quality can be facilitated by the selection of lead-like chemical starting points, control of physicochemical properties during optimization, employment of predictive chemistry tools, and the application of ligand efficiency measures.

What You Will Learn

  • Impact of compound quality on clinical pipeline attrition
  • Lead-like versus drug-like physicochemical properties
  • Application of ligand efficiency measures in optimization and candidate selection



The Fine Print

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Paul Leeson
Paul Leeson Consulting

Richard Connell

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