Whitepapers , Early Clinical Development , Clinical Pharmacology , Peptide Drug Development

How to Capture Growth in the Expanding Metabolic Drug Market

Overview

Bringing new metabolic disease therapies, such as GLP-1s, from a promising molecule to patient delivery requires seamless sponsor-CRDMO collaboration. 

Interest in the development of new therapies to treat endocrine and metabolic diseases has skyrocketed, driven in part by increased commercial success and medical efficacy of GLP-1 agonists and other incretin hormones used to treat obesity in recent years.

As a result, research and development spending in metabolic disease therapies is now on par with oncology, making it one of the most sought-after areas in the pharmaceutical industry.

In this whitepaper, Dr. Andy Lewis, Chief Scientific Officer, Dr. Andreas Reichl, Senior Drug Development Consultant, and Matthew Paterson, Chief Strategy Officer, share an inside look at what it takes to succeed in this competitive market. 

Solutions for early clinical development

Dedicated to early clinical development, Quotient Sciences can help accelerate your molecule to your first-in-human and proof of concept milestones. We also offer a range of exploratory and regulatory-driven Phase 1 clinical pharmacology studies for registration and product labelling purposes.

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Achieve your molecule’s full potential with our extensive experience in clinical testing

  • Meet your exploratory, registration and product labeling studies

Our full range of clinical pharmacology studies include DDI, human ADME, BA/BE, and more. These can be run individually or as part of a package to streamline your clinical testing.

  • Enable access to healthy volunteers and special populations

Our dedicated volunteer management teams can quickly recruit healthy volunteers and special populations, such as healthy smokers and healthy elderly, for your phase 1 study.

  • Keep you in control

Programs are led by experienced project management and medical staff, with scientific and regulatory support to keep your clinical study on-course.

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Have a question about your early clinical program? Ask a member of our team about our capabilities for clinic-ready formulations, FIH to POC studies, clinical pharmacology programs, and more.

Dr. Andrew Lewis

Chief Scientific Officer

Dr. Andrew (Andy) Lewis is the Chief Scientific Officer at Quotient Sciences. As the leader of Quotient Sciences' scientific teams...

About Andrew
Dr. Vanessa Zann

VP, Scientific Consulting, Translational Pharmaceutics & Clinical Pharmacology - USA

Dr. Vanessa Zann has over twenty-five years industry experience providing expert biopharmaceutic support to drug discovery, early ...

About Vanessa
Dr. Andreas Reichl

Senior Drug Development Consultant

Dr. Andreas Reichl has over 25 years of pharmaceutical industry experience, featuring a diverse background comprising of a medical...

About Andreas
Katie Stuart

Executive Director & Head of Commercial TP-CP USA

Katie Stuart brings 27 years of experience in the pharmaceutical industry, with a background spanning analytical chemistry and bus...

About Katie
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