Emerging injectable therapies for osteoarthritis

ABSTRACT

Osteoarthritis (OA) affects more than 240 million people worldwide. In 2016, the Osteoarthritis Research Society International submitted a report to the United States Food and Drug Administration highlighting OA as a ‘serious’ disease, and appealed for the urgent development and review of new therapies to address a significant unmet need. Despite this, international guidelines for the treatment of OA have been largely unchanged for over a decade. There is now an updated understanding that OA is more than simply a non-inflammatory ‘wear-and-tear’ process involving articular cartilage. Based on this, potential emerging therapies are being developed that target novel inflammatory, pain, and regeneration pathways. Drugs targeting the latter are being lauded as ‘Disease-Modifying Osteoarthritis Drugs’ – a concept which has so far proved elusive in OA research. While this review does not recommend a change in current practice, it should prompt readers to rethink the OA treatment paradigm. The global pandemic has added another layer of consideration when managing patients with OA. At a time when there is more strain on hospital systems, there is a need to expand our pharmacological armamentarium in order to manage OA without elective surgery and hospital admission.

KEYWORDS:

• Analgesia
• cytokine
• disease-modifying osteoarthritis drug
• hip
• inflammation
• interleukin
• injectable
• knee
• matrix extracellular phosphoglycoproteins
• osteoarthritis

Declaration of interest

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.

Reviewer disclosures

A reviewer on this manuscript was a site investigator in some trials cited in this review (Pfizer tanezumab, Astellas TrkA). Peer reviewers on this manuscript have no other relevant financial relationships or otherwise to disclose.