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Published on: June 2, 2023
Prospects of Disease-Modifying Osteoarthritis Drugs
1Department of Physical Medicine and Rehabilitation, Mandalay General Hospital, University of Medicine, Mandalay, Mandalay, Myanmar; Rheumatology Department, Royal North Shore Hospital, Institute of Bone and Joint Research, Kolling Institute, The University of Sydney, Sydney, Australia.
Abstract:
Osteoarthritis (OA) causes a massive disease burden with a global prevalence of nearly 23% in 2020 and an unmet need for adequate treatment, given a lack of disease-modifying drugs (DMOADs). The author reviews the prospects of active DMOAD candidates in the phase 2/3 clinical trials of drug development pipeline based on key OA pathogenetic mechanisms directed to inflammation-driven, bone-driven, and cartilage-driven endotypes. The challenges and possible research opportunities are stated in terms of the formulation of a research question known as the PICO approach: (1) population, (2) interventions, (3) comparison or placebo, and (4) outcomes.
Insights
Osteoarthritis treatments are lacking, but new disease-modifying drugs (DMOADs) targeting inflammation, bone, or cartilage are in development. Research opportunities exist to improve clinical trial design for these promising osteoarthritis therapies.
Area of Science:
- Rheumatology and Drug Development
- Biomedical Research and Clinical Trials
Background:
- Osteoarthritis (OA) presents a significant global health challenge, affecting nearly 23% of the population in 2020.
- Current OA treatments primarily manage symptoms, with a critical unmet need for disease-modifying osteoarthritis drugs (DMOADs).
Purpose of the Study:
- To review active DMOAD candidates in Phase 2/3 clinical trials.
- To analyze these candidates based on key osteoarthritis pathogenetic mechanisms: inflammation-driven, bone-driven, and cartilage-driven endotypes.
- To identify challenges and research opportunities for advancing OA drug development.
Main Methods:
- Literature review of DMOAD candidates in late-stage clinical development.
- Categorization of drug candidates by OA endotype.
- Framework for research question formulation using the PICO approach (Population, Intervention, Comparison, Outcome).
Main Results:
- Several DMOAD candidates targeting distinct OA endotypes are progressing through clinical trials.
- The review highlights the complexity of OA pathogenesis and the need for targeted therapeutic strategies.
- The PICO approach offers a structured method for designing future OA clinical trials.
Conclusions:
- Active research into DMOADs offers hope for improved osteoarthritis management.
- Understanding OA endotypes is crucial for developing effective, targeted therapies.
- Optimizing clinical trial design through structured approaches like PICO is essential for successful drug development.
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