Why Do Promising Therapies Stall in Development and How Can We Move Them Forward?

Author:

Wegner Craig D.1,Goodwin Andrew2,Cook Jon C.3,Allamneni Krishna4,Sohn Jane2,McVean Maralee5

Affiliation:

1. AstraZeneca Pharmaceuticals, IMED Biotech Unit, Waltham, MA, USA

2. US Food and Drug Administration, Silver Spring, MD, USA

3. Pfizer Worldwide Research and Development, Groton, CT, USA

4. Jazz Pharmaceuticals, Inc, Palo Alto, CA, USA

5. PreClinical Research Services, Inc, Fort Collins, CO, USA

Abstract

There are many reasons that molecules fail to progress to market and various principles of risk–benefit decisions that can help drive the molecule through development. This symposium included discussions on global strategies involved in pushing promising molecules to market, what to do when a molecule stalls in its progress to market, and options for rescuing the molecule and pushing it forward again. Innovative partnerships that bring stalled drugs back into clinical development were also addressed. A regulatory perspective on common reasons for a molecule to fail in its forward progress was presented. In addition, situations arise when a third-party advisory committee can provide input to help overcome issues identified by a regulatory agency. Using examples from the private and public domain, presentations centered on how to repurpose a molecule and when more science is needed.

Publisher

SAGE Publications

Subject

Toxicology

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1. Introduction to Issue Resolution;Advanced Issue Resolution in Safety Pharmacology;2019

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