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Search results for: biosimilars

Arthritis Patients Lack Knowledge about Safe Use of Biologics

Will Boggs, MD  |  June 15, 2016

NEW YORK (Reuters Health)—Many patients with arthritis lack the knowledge to use their biologic treatments safely, researchers from France report. “Some patients are at risk of poorly managing their biologic therapy, especially patients living alone, in a large city, patients with low education level, or (patients who are) unemployed,” Dr. Anne-Christine Rat from CHU de…

Filed under:Biologics/DMARDsDrug Updates Tagged with:ArthritisBiologicspatient education

Samsung Bioepis Receives Final European Approval for Its Remicade Copy

Reuters Staff  |  June 1, 2016

SEOUL (Reuters)—South Korea’s Samsung Bioepis said on Monday its biosimilar of Johnson & Johnson’s blockbuster rheumatoid arthritis drug Remicade (infliximab) has received final approval from European regulators, paving the way for its second product launch in Europe. Samsung Bioepis, an unlisted arm of South Korea’s top conglomerate Samsung Group, also said last week the biosimilar…

Filed under:Biologics/DMARDsDrug Updates Tagged with:Biosimilarsinfliximabinfliximab-dyybInternationalRemicade

Roche & Novartis Face Off in Biosimilar Drug Battle

John Miller  |  May 31, 2016

ZURICH (Reuters)—Switzerland’s biggest drugmakers are clashing over cheaper copies of pricey biotech drugs—one reason why Novartis is considering selling its $14 billion stake in cross-town rival Roche. With a copycat of Roche’s blood cancer drug Rituxan (rituximab) pending European approval, Novartis aims to muscle in on a share of sales that last year hit 7…

Filed under:Drug Updates Tagged with:BiosimilarsBusinessgeneric drugsNovartisRemicaderituximabRoche

Rheumatology Drug Updates: Infliximab Biosimilar Gets FDA Approval & More

Michele B. Kaufman, PharmD, BCGP  |  May 13, 2016

April 5, 2016, marks a revolutionary day in the treatment of autoimmune diseases: The U.S. Food and Drug Administration (FDA) approved an infliximab (Remicade) biosimilar, known as Inflectra (infliximab-dyyb). Infliximab-dyyb, which is administered by intravenous infusion, is the first biosimilar drug approved to treat rheumatic disease in the U.S.1 Infliximab-dyyb has received approval for almost…

Filed under:Biologics/DMARDsDrug UpdatesResearch Rheum Tagged with:ApprovalsBiologicsBiosimilarsdrugFDAInflectrainfliximabRemicadeResearchrheumatologySafetyZirletta

Triple Therapy with Methotrexate Effective, Cheaper in RA

Larry Hand  |  April 27, 2016

NEW YORK (Reuters Health)—The combination of methotrexate, sulphasalazine and hydroxychloroquine is similar in effect as methotrexate plus biologic therapy for patients with rheumatoid arthritis (RA), according to a new network meta-analysis. “Thus, for most patients, this low-cost combination of medications should probably be tried before moving onto biologic therapy, either as initial treatment or as…

Filed under:ConditionsDrug UpdatesRheumatoid Arthritis Tagged with:BiologicsHYDROXYCHLOROQUINEMethotrexateRheumatoid Arthritis (RA)sulphasalazinetriple therapy

2015 ACR/ARHP Annual Meeting: Cellular Triggers in Inflammatory Disease

Susan Bernstein  |  April 14, 2016

SAN FRANCISCO—What factors help determine whether or not inflammation resolves, leading to healing, or becomes chronic, leading to disease and tissue destruction? A number of important cells, including toll-like receptors, mast cells, anti-citrullinated protein antibodies, complement and interferon, all play their own role in this process. By understanding how they act in innate and adaptive…

Filed under:ConditionsMeeting ReportsOther Rheumatic ConditionsResearch Rheum Tagged with:2015 ACR/ARHP Annual MeetingAmerican College of Rheumatology (ACR)anti-citrullinated protein antibodiescellsInflammatory Diseaseinterferonmast cellPathogenesisResearchrheumatologisttoll-like receptor

From the Expert: Don’t Forget to Vaccinate Immuncompromised Patients

Richard Quinn  |  April 8, 2016

Preventing infection in immunocompromised patients is challenging, especially with the increased use of biologic treatments, which have been known to reactivate latent infections, such as the herpes zoster virus. Nicolas Issa, MD, discusses recent vaccination research and prevention techniques to help this patient group avoid infection…

Filed under:Conditions Tagged with:BiologicsherpesInfectionpreventionvaccination

Infliximab Biosimilar Receives FDA Approval

Michele B. Kaufman, PharmD, BCGP  |  April 6, 2016

The FDA has officially approved an infliximab biosimilar for the treatment of multiple autoimmune diseases, including rheumatoid arthritis, psoriatic arthritis and ankylosing spondylitis. Prescribing information is now available…

Filed under:Biologics/DMARDsDrug Updates Tagged with:FDAFood and Drug Administrationinfliximabinfliximab-dyyb

FDA Approves Biosimilar to J&J’s Remicade for Multiple Diseases

Reuters Staff  |  April 6, 2016

(Reuters)—The U.S. Food and Drug Administration on Tuesday approved Inflectra, a cheaper version of Johnson & Johnson’s drug Remicade (infliximab), to treat Crohn’s disease, ulcerative colitis, rheumatoid arthritis, psoriasis and arthritis of the spine. Inflectra, also known as infliximab-dyyb, is expected by some analysts to sell for a 25% discount to Remicade, which generated annual…

Filed under:Biologics/DMARDsDrug Updates Tagged with:BiosimilarsFDAFood and Drug Administrationinfliximabinfliximab-dyyb

Biosimilar Drugs Could Save Up to $110 Billion by 2020

Reuters Staff  |  March 30, 2016

LONDON (Reuters)—Lower-cost copies of complex biotech drugs, known as biosimilars, could save the U.S. and Europe’s five top markets as much as 98 billion euros ($110 billion) by 2020, a new analysis showed on Tuesday. Realizing those savings, however, depends on effective doctor education and healthcare providers adopting smart market access strategies, the report by…

Filed under:Biologics/DMARDsDrug Updates Tagged with:adalimumabBiosimilarscostshealthcare costTreatment costs

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