2020
DOI: 10.1016/j.semarthrit.2020.03.004
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Onset and maintenance of efficacy of subcutaneous tanezumab in patients with moderate to severe osteoarthritis of the knee or hip: A 16-week dose-titration study

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Cited by 15 publications
(25 citation statements)
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“…The early and sustained efficacy of tanezumab seen in the current study in patients enrolled in Europe and Japan is supported by a previous study in North America with primary endpoints at Week 16 (Schnitzer et al., 2020 ). Both studies showed greater improvement from baseline in WOMAC Pain, Physical Function and PGA‐OA scores (LS mean) at Week 16 for tanezumab compared with placebo.…”
Section: Discussionsupporting
confidence: 84%
See 1 more Smart Citation
“…The early and sustained efficacy of tanezumab seen in the current study in patients enrolled in Europe and Japan is supported by a previous study in North America with primary endpoints at Week 16 (Schnitzer et al., 2020 ). Both studies showed greater improvement from baseline in WOMAC Pain, Physical Function and PGA‐OA scores (LS mean) at Week 16 for tanezumab compared with placebo.…”
Section: Discussionsupporting
confidence: 84%
“…Studies using intravenous administration of the nerve growth factor monoclonal antibody, tanezumab, showed early and sustained efficacy in patients with hip or knee OA (Brown et al, 2012(Brown et al, , 2013Lane et al, 2010;Spierings et al, 2013). A dose-titration study of subcutaneous tanezumab in patients in North America with hip or knee OA demonstrated efficacy within the first week that was generally sustained over a 16-week treatment period (Schnitzer et al, 2019(Schnitzer et al, , 2020.…”
Section: Introductionmentioning
confidence: 99%
“…A few cases of RPOA and TJRs were observed. Similarly, in two different clinical trials, Schnitzer et al 50 , 51 showed that tanezumab improved all outcomes of patients with knee or hip OA. With regard to adverse effects, TJRs and RPOA were more evident in the tanezumab than in the placebo group, in a dose-dependent manner.…”
Section: Adverse Effects Of Anti-ngf Mab Therapy For Oa: An Update On the Clinical Trialsmentioning
confidence: 87%
“…Biological treatments that target OA, attenuate catabolic activity and promote articular cartilage repair include purified or recombinant growth factors, including fibroblast growth factor 18 (FGF-18), also known as Sprifermin [52][53][54], bone morphogenic protein 7 (BMP7) [55,56], transforming growth factor β1 (TGF-β1) [57][58][59], neuropeptides [60,61], humanized mAbs that target NGF and vascular endothelial growth factor (VEGF) (i.e., tanezumab (Pfizer) and fasinumab (Teva/Regeneron) against NGF and bevacizumab (Genentech/Roche) and ranibizumab (Genentech/Roche) against VEGF) [62][63][64][65][66], gene and cell therapy incorporating allogeneic cells and protein production platforms that overproduce produce growth factors (i.e., Kolon TissueGene's TissueGene-C, overproducing TGF-β1) [67][68][69][70][71] (Figure 2). A detailed discussion of each of these areas and intra-articular therapies is way beyond the scope of this communication and readers are directed to several comprehensive reviews [72][73][74][75].…”
Section: Emerging Biological Treatments For Oamentioning
confidence: 99%