2020
DOI: 10.1038/s41584-020-00518-6
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Emerging pharmaceutical therapies for osteoarthritis

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Cited by 280 publications
(222 citation statements)
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“…Thus, the guidelines from the United States Food and Drug Administration (FDA) and the European Medicines Agency (EMA) point out that the effective diseasemodifying osteoarthritis drugs (DMOADs) should be developed (Reginster et al, 2015;Oo et al, 2018). A DMOAD is expected a drug that modifies the underlying OA pathophysiology, thereby inhibiting structural damage to prevent or reduce long-term disability and offer potential symptomatic relief (Latourte et al, 2020). Currently, there are no US FDA-or EMAapproved DMOADs.…”
Section: Infliximabmentioning
confidence: 99%
See 1 more Smart Citation
“…Thus, the guidelines from the United States Food and Drug Administration (FDA) and the European Medicines Agency (EMA) point out that the effective diseasemodifying osteoarthritis drugs (DMOADs) should be developed (Reginster et al, 2015;Oo et al, 2018). A DMOAD is expected a drug that modifies the underlying OA pathophysiology, thereby inhibiting structural damage to prevent or reduce long-term disability and offer potential symptomatic relief (Latourte et al, 2020). Currently, there are no US FDA-or EMAapproved DMOADs.…”
Section: Infliximabmentioning
confidence: 99%
“…With the population aging and obesity, the incidence of OA is increasing as a leading cause of disability worldwide (Peat and Thomas, 2020). To date, no effective drug is able to inhibit the structural damage or reduce long-term disability, or relieve pain with an acceptable benefit-to-risk profile in OA (Latourte et al, 2020). For these reasons, the OARSI led an effort to submit a White Paper to the FDA in support of the designation of OA as a serious disease in 2016.…”
Section: Expert Opinionmentioning
confidence: 99%
“…Most trials conducted to date have produced inconclusive results [47]. This means that the novel pharmacological agents, disease-modifying OA drugs (DMOADs) [48][49][50] and biological interventions that are currently being tested must have an impact on joint structure (i.e., articular cartilage) and the symptoms of pain, even if the trials include surrogate endpoints and post-marketing confirmatory data under the accelerated drug approval regulations set forth by the Food and Drug Administration (FDA) [51].…”
Section: Existing Recommended Treatments For Oamentioning
confidence: 99%
“…Most trials conducted to date producing inconclusive results [26]. This means that the novel pharmacological agents, disease-modifying OA drugs (DMOADs) [27][28][29] and biological interventions that are currently being tested need to impact on joint structure (i.e. articular cartilage) and the symptoms of pain, even if they include surrogate endpoint and post-marketing confirmatory data under the accelerated drug approval regulations set forth by the Food and Drug Administration (FDA) [30].…”
Section: Existing Recommended Treatments For Oamentioning
confidence: 99%