May 24, 2022 News by Marta Figueiredo, PhD High Adherence to Rebif Seen With RebiSmart Use, Chats With Doctor Regular feedback from doctors about dosing data and health status is associated with high and sustained treatment adherence to RebifĀ (interferon beta-1a) amongĀ multiple sclerosis (MS)Ā patients using the RebiSmart autoinjector, a two-year observational study shows. This study’s level of treatment adherence ā 97.9% ā was comparable or superior to the…
April 25, 2022 News by Marta Figueiredo, PhD Plegridy Found at Minimal Levels in Breast Milk, Small Study Reports Plegridy (peginterferon beta-1a), an approved treatment for relapsing multiple sclerosis (MS), is detected at minimal concentrations in the breast milk of patients using the therapy postpartum, a small study showed. This is in line with label updates on Plegridy and other interferon beta therapies in EuropeĀ and…
February 2, 2021 News by Marisa Wexler, MS FDA Approves Plegridy as Intramuscular Injection for Relapsing MS The U.S. Food and Drug Administration (FDA) has approved an intramuscular injectionĀ formulation of Plegridy (peginterferon beta-1a) to treat people with relapsing forms of multiple sclerosis (MS). This formulation, for injection directly into muscle, is what is typically used to deliver the flu shot. According to Biogen, Plegridy’s…
December 22, 2020 News by Joana Carvalho, PhD Plegridy as Intramuscular Injection for RRMS Approved in Europe The European Commission (EC) has approved a new, intramuscular formulation of Plegridy (peginterferon beta-1a) to treat people with relapsing-remitting multiple sclerosis (RRMS). This new mode of administration ā in which Plegridy is directly injected into the muscle, rather than under the skin (subcutaneously) ā does…
January 27, 2020 News by Marisa Wexler, MS NICE Approves Plegridy as RRMS Treatment Offered by NHS England The National Institute for Health Care and Excellence (NICE) in the U.K. issued its final decision, approving the inclusion of Plegridy (peginterferon beta-1a) to treatĀ relapsing-remitting multiple sclerosis (RRMS) in England within the National Health Service (NHS). This decision follows a cost-effectiveness review done in May 2018,…
September 12, 2019 News by Joana Carvalho, PhD #ECTRIMS2019 ā Biogen Presents New Real-world Data Demonstrating Clinical Benefits of Tysabri, Plegridy, and Avonex Biogen is presenting new data highlighting the potential clinical benefits of Tysabri (natalizumab), Plegridy (peginterferon beta-1a), and Avonex (interferon beta-1a) for the treatment of specific groups of individuals with multiple sclerosis (MS), including pregnant women and patients with relapsing forms of the disease. The new…
October 5, 2018 Columns by Ed Tobias Could Government Probe Threaten Pharma Patient Assistance Programs? Many of us have received help to pay for our MS medications. Now there’s a chance that assistance could be threatened. A recent article in the The Wall Street Journal reports that U.S. government prosecutors are looking into whether some pharmaceutical companies’ patient assistance programs are on the wrong…
July 22, 2015 News by Patricia Silva, PhD NHS Wales Approves Biogen’s Plegridy for Relapsing Remitting MS Relapsing remitting multiple sclerosis (RRMS) treatment PlegridyĀ (peg interferon beta-1a) by Biogen Idec, has just received Welsh NHS approval, which should make it available to patients by late October 2015. The decisionĀ follows NHS Scotland’s approval earlier this year, however, theĀ biweekly interferon beta shot has yet to be madeĀ available in England’s NICE…
August 20, 2014 News by admin New Relapsing-Remitting Multiple Sclerosis Drug Approved By FDA Biogen Idec, a biotechnology company focused on developing innovative therapies for the treatment of neurodegenerative diseases, hematologic conditions and autoimmune disorders, has announced that the U.S. Food and Drug Administration (FDA) has approved PLEGRIDYTMĀ (peginterferon beta-1a), a new treatment for people with relapsing forms of multiple sclerosis…