Reflections from the OARSI 2022 clinical trials symposium: The pain of OA-Deconstruction of pain and patient-reported outcome measures for the benefit of patients and clinical trial design.


Journal

Osteoarthritis and cartilage
ISSN: 1522-9653
Titre abrégé: Osteoarthritis Cartilage
Pays: England
ID NLM: 9305697

Informations de publication

Date de publication:
10 2023
Historique:
received: 08 10 2022
revised: 01 06 2023
accepted: 19 06 2023
medline: 18 9 2023
pubmed: 29 6 2023
entrez: 28 6 2023
Statut: ppublish

Résumé

Osteoarthritis (OA) drug development is hampered by a number of challenges. One of the main challenges is the apparent discordance between pain and structure, which has had a significant impact on drug development programs and has led to hesitance among stakeholders. Since 2017, the Clinical Trials Symposium (CTS) has been hosted under the Osteoarthritis Research Society International (OARSI) leadership. OARSI and the CTS steering committee yearly invite and encourage discussions on selected special subject matter between regulators, drug developers, clinicians, clinical researchers, biomarker specialists, and basic scientists to progress drug development in the OA field. The main topic for the 2022 OARSI CTS was to elucidate the many facets of pain in OA and to enable a discussion between regulators (Food and Drug Administration (FDA) and the European Medicines Agency (EMA)) and drug developers to clarify outcomes and study designs for OA drug development. Signs or symptoms indicative of nociceptive pain occur in 50-70% of OA patients, neuropathic-like pain in 15-30% of patients, and nociplastic pain in 15-50% of patients. Weight-bearing knee pain is associated with bone marrow lesions and effusions. There are currently no simple objective functional tests whose improvements correlate with patient perceptions. The CTS participants, in collaboration with the FDA and EMA, raised several suggestions that they consider key to future clinical trials in OA including the need for more precise differentiation of pain symptoms and mechanisms, and methods to reduce placebo responses in OA trials.

Identifiants

pubmed: 37380011
pii: S1063-4584(23)00830-0
doi: 10.1016/j.joca.2023.06.006
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1293-1302

Subventions

Organisme : NIAMS NIH HHS
ID : P30 AR072571
Pays : United States

Informations de copyright

Copyright © 2023 Osteoarthritis Research Society International. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest None.

Auteurs

M A Karsdal (MA)

Nordic Bioscience, Herlev, Denmark; Southern Danish University, Odense, Denmark. Electronic address: MK@nordicbio.com.

J Tambiah (J)

Biosplice Therapeutics, San Diego, USA.

D Felson (D)

Boston University School of Medicine, Boston, MA, USA.

C Ladel (C)

CHL4special Consultancy, Darmstadt, Germany.

N P Nikolov (NP)

Office of New Drugs, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA.

D Hodgins (D)

Dynamic Metrics Limited, Codicote, UK.

A R Bihlet (AR)

NBCD A/S, Herlev, Denmark.

T Neogi (T)

Boston University School of Medicine, Boston, MA, USA.

C Baatenburg de Jong (C)

Dutch Arthritis Society, Amsterdam, the Netherlands.

A C Bay-Jensen (AC)

Nordic Bioscience, Herlev, Denmark.

R Baron (R)

University Medical Center Schleswig-Holstein (UKSH), Campus Kiel, Kiel, Germany.

A Laslop (A)

Committee for Medicinal Products for Human Use (CHMP), European Medicines Agency, Amsterdam, the Netherlands; Bundesamt für Sicherheit im Gesundheitswesen (BASG), Vienna, Austria.

A Mobasheri (A)

Research Unit of Health Sciences and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland; Department of Regenerative Medicine, State Research Institute Centre for Innovative Medicine, Vilnius, Lithuania; Department of Joint Surgery, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China; World Health Organization Collaborating Centre for Public Health Aspects of Musculoskeletal Health and Aging, Université de Liège, Liege, Belgium.

V B Kraus (VB)

Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC, USA.

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