<\/p>\n
La Force is happy to share this press release provided by Santhera Pharmaceuticals<\/a><\/span>, October 7, 2019, > PRESS RELEASE<\/a><\/span>\u00a0<<\/p>\n <\/p>\n Santhera Pharmaceuticals announces the presentation of data showing continued improvement of muscle function and improved tolerability compared with corticosteroids of 18-month vamorolone treatment in Duchenne muscular dystrophy (DMD). These top-line data were presented on October 5 by Eric Hoffman, Ph.D., CEO of ReveraGen at the\u00a0<\/span><\/strong>World Muscle Society (WMS)<\/strong><\/a><\/span>\u00a0congress.<\/span><\/strong><\/p>\n In a late-breaking presentation at the WMS international conference in Copenhagen, Denmark, ReveraGen presented motor function and tolerability data from 23 DMD patients treated with 2.0 or 6.0 mg\/kg\/day with vamorolone for at least 18 months in the ongoing VBP15-LTE<\/a><\/span> study.<\/p>\n <\/p>\n Eric Hoffman, Ph.D., Chief Executive Officer of ReveraGen –<\/strong> “These data demonstrate that vamorolone treatment results in persistently improved motor function in DMD patients, similar to that of corticosteroids. Importantly, however, vamorolone treatment over a period of 18 months showed better tolerability with less corticosteroid-specific side effects, including no stunting of the growth of DMD children.”<\/p><\/blockquote>\n <\/p>\n Vamorolone is a first-in-class steroidal anti-inflammatory investigational drug in development as a treatment for DMD to substitute standard corticosteroids (prednisone, deflazacort). This trial is an extension study of the VBP15-003 trial in which 48 DMD patients treated for 6 months over a broad dose range (0.25 to 6.0 mg\/kg\/day) showed dose-related improvements in multiple gross motor outcomes. Upon exiting this 6-month trial, patients and their physicians preferred to continue vamorolone treatment. 45 boys transitioned to the 2-year long-term extension study VBP15-LTE and all doses were increased to 2.0 or 6.0 mg\/kg\/day of vamorolone.<\/p>\n At the WMS conference, Dr. Hoffman presented data from 23 patients treated with 2.0 or 6.0 mg\/kg\/day vamorolone for at least 18 months. Vamorolone treatment consistently and significantly improved standardized motor function outcomes measured as velocity to stand from supine, to run\/walk 10 meters and to climb 4 stairs from baseline to month 18. Motor function outcomes for vamorolone treated patients also were consistently better than outcomes for age-matched, steroid na\u00efve patients from an external natural history study<\/strong> (velocity to stand from supine: p=0.085; run\/walk 10 meters: p=0.005; climb 4 stairs: p=0.036; all in favour of vamorolone treatment).<\/p>\n Motor function outcomes of vamorolone-treated DMD boys were compared to age-matched prednisone-treated patients from an external control group. Both vamorolone and prednisone treated groups showed similar improvements in these gross motor outcomes, demonstrating that vamorolone exerts therapeutic efficacy similar to standard corticosteroids. Importantly, vamorolone-treated boys showed normal growth rates, and less physician-reported weight gain and Cushingoid features compared to published studies of prednisone and deflazacort. These findings confirm earlier data that indicate a better tolerability profile of vamorolone compared to standard corticosteroids.<\/strong><\/p>\n Together with previously reported molecular and clinical data, the new 18-month data suggest that dissociative steroidal drug vamorolone maintains efficacy and decreases adverse effects typically reported for corticosteroids in the treatment of DMD. Vamorolone has been granted Orphan Drug status in the US and Europe and has received Fast Track and Rare Pediatric Disease designations by the US FDA.<\/p>\n Vamorolone is a first-in-class drug candidate that binds to the same receptors as corticosteroids but modifies the downstream activity of the receptors. This has the potential to \u2018dissociate\u2019 efficacy from typical steroid safety concerns and therefore could replace existing corticosteroids, the current standard of care in children and adolescent patients with DMD. There is a significant unmet medical need in this patient group as high dose corticosteroids have severe systemic side effects that detract from treatment compliance and patient quality of life.<\/p>\n The currently ongoing 48-week Phase IIb VISION-DMD<\/a><\/span> study is designed as a pivotal trial to demonstrate efficacy and safety of vamorolone compared with prednisone and placebo in 120 boys aged 4 to <7 with DMD that have not yet been treated with corticosteroids. Vamorolone is being developed by US-based ReveraGen BioPharma Inc<\/a><\/span>. with participation in funding and design of studies by several international non-profit foundations, the US National Institutes of Health, the US Department of Defense and the European Commission\u2019s Horizon 2020 program. In November 2018, Santhera<\/a><\/span> acquired from Idorsia<\/a><\/span> the option to an exclusive sub-license to vamorolone in all indications and all countries worldwide (except Japan and South Korea).<\/p>\n Clinical trial in Canada<\/a><\/span><\/p>\n Santhera Pharmaceuticals is a Swiss specialty pharmaceutical company focused on the development and commercialization of innovative medicines for rare neuromuscular and pulmonary diseases with a high unmet medical need. Santhera is building a Duchenne muscular dystrophy (DMD) product portfolio to treat patients irrespective of causative mutations, disease stage or age. A marketing authorization application for Puldysa\u00ae (idebenone)<\/a><\/span> is currently under review by the European Medicines Agency. Santhera has an option to license vamorolone, a first-in-class dissociative steroid currently investigated in a pivotal study in patients with DMD to replace standard corticosteroids. Santhera out-licensed ex-North American rights to its first approved product, For further information, please visit www.santhera.com. Raxone\u00ae and Puldysa\u00ae are trademarks of Santhera Pharmaceuticals<\/em><\/p>\n ReveraGen was founded in 2008 to develop first-in-class dissociative steroidal drugs for Duchenne muscular dystrophy and other chronic inflammatory disorders. The development of ReveraGen\u2019s lead compound, vamorolone, has been supported through partnerships with foundations worldwide, including Muscular Dystrophy Association USA<\/a><\/span>, Parent Project Muscular Dystrophy<\/a><\/span>, Foundation to Eradicate Duchenne<\/a><\/span>, Save Our Sons<\/a><\/span>, JoiningJack<\/a><\/span>, Action Duchenne<\/a><\/span>, CureDuchenne<\/a><\/span>, Ryan\u2019s Quest<\/a><\/span>, Alex\u2019s Wish<\/a><\/span>, DuchenneUK<\/a><\/span>, Pietro\u2019s Fight<\/a><\/span>, Michael\u2019s Cause<\/a><\/span>, and Duchenne Research Fund<\/a><\/span>. ReveraGen has also received generous support from the US Department of Defense CDMRP, National Institutes of Health (NCATS, NINDS, NIAMS), and European Commission (Horizons 2020).<\/p>\n Santhera Announces Presentation by ReveraGen of Positive 18-Month Data with Vamorolone in Duchenne Muscular Dystrophy La Force is happy to share this press release provided by Santhera Pharmaceuticals, October 7, 2019, > PRESS RELEASE\u00a0< Santhera Pharmaceuticals announces the presentation of data showing continued improvement of muscle function and improved tolerability compared with corticosteroids […]<\/p>\n","protected":false},"author":2,"featured_media":8934,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[12,17,18],"tags":[],"class_list":["post-8927","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news","category-research","category-treatments"],"yoast_head":"\nVamorolone compared to standard corticosteroids<\/h4>\n
About Vamorolone \u2013 first-in-class dissociative steroid<\/h4>\n
About Santhera<\/h4>\n
About ReveraGen BioPharma<\/h4>\n
Links<\/h4>\n
\n