March 20, 2019 News by Jose Marques Lopes, PhD SPMS Treatment With Mayzent Better Than Best Supportive Care, ICER Report Says Treatment of secondary progressive multiple sclerosis (SPMS) patients with the investigational oral therapy Mayzent (siponimod) significantly reduced the risk of disability progression and decreased inflammation, compared to best supportive care, according to aĀ preliminary draft evidence reportĀ from the Institute for Clinical and Economic Review (ICER). The report…
October 17, 2018 News by Jose Marques Lopes, PhD #ECTRIMS2018 – Blood Level of Neurofilament Light Chain May Predict Brain Atrophy in Progressive MS, Study Suggests Measuring the blood level of neurofilament light chain (NfL) may predict brain shrinkage in primary progressive (PPMS) and secondary progressive multiple sclerosis (SPMS), according to a new study. The findings also show that NfL levels are associated with brain lesion load in these patients. The research, ā…
October 15, 2018 News by BioNews Staff #ECTRIMS2018 ā As Siponimod Awaits FDA Decision, Mouse Work Helps in Understanding Benefits Seen in SPMS Mouse studies ofĀ siponimod ā a potential progressive multiple sclerosis (MS) treatment that’s up for approval in the U.S. and EU ā were among presentations given by NovartisĀ at the 34th European Committee for Treatment and Research in Multiple SclerosisĀ (ECTRIMS), held Oct. 10-12 in Berlin. Animal work might seem…
October 10, 2018 News by Alice MelĆ£o, MSc FDA, EMA Agree to Review Novartis Therapy Siponimod to Treat SPMS Novartis is seeking U.S. and European approval of its investigational oral agent siponimodĀ to treat adults with secondary progressive multiple sclerosis (SPMS). The U.S. Food and Drug Administration (FDA) has accepted for review the company’s New Drug Application, while the European Medicines Agency (EMA) has accepted for review…
September 21, 2018 News by Alice MelĆ£o, MSc Ocrevus Climbing as First-line DMT for RRMS Among Neurologists Surveyed in Spherix Report Eighteen months after its entrance into the U.S. market,Ā Genentechās Ocrevus (ocrelizumab) has become the monoclonal antibody of choice to treat patients with multiple sclerosis (MS), according to a survey of nearly 100 neurologists across the U.S. Self-reported use of Ocrevus for theĀ third quarter of 2018 surpassed…
June 27, 2018 News by Patricia Inacio, PhD After Ocrevus Approval, New Therapies May Become Available for MS, Report Suggests Genentech‘s OcrevusĀ (ocrelizumab),Ā approved in March 2017, has fueled a sea change in the treatment of multiple sclerosis (MS) patients in the U.S., leading to an increased interest in disease-modifying therapies (DMTs) for progressive forms of MS. Now, other potential treatment choices for progressive MS forms will likely…
April 27, 2018 News by Jose Marques Lopes, PhD #AAN2018 – Siponimod Lessens Risk of SPMS Progression Independent of Relapses, Trial Data Show Novartisā investigational oral treatmentĀ siponimod (BAF312) reduces the risk of disability progression in patients with secondary progressive multiple sclerosis (SPMS), a new analysis of Phase 3 trial results show. Using what the company describes as more accurate methods to assess siponimod effect’s on progression risk, necessary because the…
April 17, 2018 News by Alice MelĆ£o, MSc #AAN2018 ā Siponimod Reduces Disease Activity Biomarker in SPMS Patients Novartis‘ siponimod (BAF312) can reduce blood levels of a biomarker of nerve cell damage in patients with secondary progressive multiple sclerosis (SPMS), a Phase 3 clinical trial shows. Researchers will present the latest results of the ongoing trial at the 2018 annual meeting of the American Academy…
March 27, 2018 News by Alice MelĆ£o, MSc Siponimod Reduces Risk of SPMS Patients’ Disability Worsening, Phase 3 Trial Shows Siponimod (BAF312) reduces the risk of disability progression in patients withĀ secondary progressive multiple sclerosis (SPMS), a Phase 3 clinical trial shows. An article about theĀ NovartisĀ therapy’s trial resultsĀ appeared in the journal The Lancet. The title is āSiponimod versus placebo in secondary progressive multiple sclerosis…
March 15, 2018 News by Patricia Inacio, PhD New Spherix Report Finds PPMS Treatment Increased Significantly in Past Year Since Genentech‘sĀ OcrevusĀ was approvedĀ a year ago, the treatment rate of primary progressive multiple sclerosis (PPMS)Ā has increased significantly. However, a closer look at the data shows that other disease-modifying therapies (DMTs) are equally responsible for this increase. The findings were reported byĀ Spherix Global InsightsĀ in their new study…
October 30, 2017 News by Patricia Silva, PhD #MSParis2017 ā Promising Work in Pediatric and Secondary Progressive Patients Is Focus, Novartis Says in Interview Gilenya (fingolimod) lowered relapse rates in children and adolescents with relapsing multiple sclerosis at a “magnitude” ā almost 82 percent ā never before seen in a scientific study and could be “life changing” for these hard-to-treat patients, a top researcher withĀ Novartis, the treatment’s developer, said in an…
October 26, 2017 News by Patricia Silva, PhD #MSParis2017 – Siponimod Leads to Dramatic Drop in MS Lesions, Phase 3 Trial Shows Novartis’Ā SiponimodĀ led to a dramatic drop in the number of inflammation patches in the brains and spinal cords of secondary progressive multiple sclerosis patients, according to a Phase 3 clinical trial. Robert Fox of the Cleveland Clinic’sĀ Mellen Center for Treatment and Research in Multiple SclerosisĀ presented the findings…
June 2, 2017 News by Patricia Silva, PhD #CMSC17 – Ocrevus, Progressive MS and Other Research Highlights: An Interview with CMSC’s Robert Lisak The recent annual meeting of theĀ Consortium of Multiple Sclerosis Centers (CMSC)Ā brought researchers and healthcare professionals to New Orleans to discuss advances ā and obstacles to advances ā in multiple sclerosis (MS) research. Clinical trials, preclinical studies, basic research, and health interventions were amongĀ the May meeting’s focus. Multiple Sclerosis News…
April 28, 2017 News by Joana Fernandes, PhD Siponimod Slows Progression of MS Disability, Phase 3 Clinical Trial Shows SiponimodĀ slows the progression of multiple sclerosis patients’ disability, a Phase 3 clinical trial indicates. The therapy reduced the risk of disability progression in patients with secondary progressive multiple sclerosis (SPMS) by 21 percent over three months, researchers said. At six months, the reduction was 26 percent, they said. Researchers…
September 21, 2016 News by Patricia Silva, PhD #ECTRIMS2016 – Novartis’s Siponimod Appears to Slow SPMS Progression in Phase 3 Study AĀ presentation at the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) 2016 Congress gave patients with progressive multiple sclerosis (MS) a reason for optimism, as Novartis reported that siponimod (BAF312) reduced the risk of disability progression in a Phase 3 study of patients with secondary progressive (SP) MS.
September 5, 2016 Columns by admin MS Patientās Pick of the Weekās News: Siponimod, Thymosin Patent, Orphan Drug, Lifestyle, and Lymphopenia Risk Hereās my Pick of the Weekās News, as published in Multiple Sclerosis News Today. Gilenya-like Therapy Shows Benefit in Secondary Progressive MS Patients in Phase 3 Trial Hereās a potentially encouraging development for anyone with SPMS. Patients withĀ secondary progressive multiple sclerosisĀ (SPMS) who were treated withĀ BAF312 (siponimod),…
August 29, 2016 News by InĆŖs Martins, PhD Gilenya-like Therapy Shows Benefit in Secondary Progressive MS Patients in Phase 3 Trial Patients with secondary progressive multiple sclerosis (SPMS) who were treated with BAF312 (siponimod), a sphingosine-1-phosphate (S1P) inhibitor, in a Phase 3 clinical trial showed aĀ Ā significantly reduced risk for disability progression compared to placebo,Ā NovartisĀ recently announced. BAF312 is a selective modulator of specific types of the S1P receptor. This receptor is…
September 12, 2014 News by Patricia Silva, PhD Novartis Presents Impressive Gilenya Updates at MSBoston 2014 This past Wednesday, September 10th, the largest, most anticipated multiple sclerosis (MS) convention — the 6th Joint ACTRIMS-ECTRIMS Triennial Meeting, MSBoston 2014 — kicked off with a whopping 8,000 registered attendees, all eager to learn more about the latest developments in MS. One of the highlights of the event…