The current state of the osteoarthritis drug development pipeline: a comprehensive narrative review of the present challenges and future opportunities

Author:

Kim Heungdeok1,Seo Jinwon1,Lee Yunsin1,Park Kiwon1,Perry Thomas A.2,Arden Nigel K.34,Mobasheri Ali56789,Choi Heonsik10ORCID

Affiliation:

1. Institute of Bio Innovation Research, Kolon Life Science, Inc., Seoul, South Korea

2. Centre for Osteoarthritis Pathogenesis Versus Arthritis, Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK

3. Versus Arthritis Centre for Sport, Exercise and Osteoarthritis, University of Oxford, Oxford, UK

4. Botnar Research Centre, Nuffield Orthopaedic Centre, Oxford, UK

5. Research Unit of Medical Imaging, Physics and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland

6. Department of Regenerative Medicine, State Research Institute Center for Innovative Medicine, Vilnius, Lithuania

7. Department of Orthopedics and Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, The Netherlands

8. Department of Joint Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China

9. World Health Organization Collaborating Center for Public Health Aspects of Musculoskeletal Health and Aging, Université de Liège, Liège, Belgium

10. Healthcare Research Institute, Kolon Advanced Research Center, Kolon Industries, Inc., 110 Magokdong-ro, Gangseo-gu, Seoul 07793, South Korea

Abstract

In this narrative review article, we critically assess the current state of the osteoarthritis (OA) drug development pipeline. We discuss the current state-of-the-art in relation to the development and evaluation of candidate disease-modifying OA drugs (DMOADs) and the limitations associated with the tools and methodologies that are used to assess outcomes in OA clinical trials. We focus on the definition of DMOADs, highlight the need for an updated definition in the form of a consensus statement from all the major stakeholders, including academia, industry, regulatory agencies, and patient organizations, and provide a summary of the results of recent clinical trials of novel DMOAD candidates. We propose that DMOADs should be more appropriately targeted and investigated according to the emerging clinical phenotypes and molecular endotypes of OA. Based on the findings from recent clinical trials, we propose key topics and directions for the development of future DMOADs.

Publisher

SAGE Publications

Subject

Orthopedics and Sports Medicine,Rheumatology

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