Bayer

Consecutive Use of Gilenya and Lemtrada Causes Disease Activity in MS Patient, Case Report Suggests

Multiple sclerosis (MS) patients may experience severe disease exacerbation after switching fromĀ Novartisā€™Ā Gilenya (fingolimod) to Sanofi Genzymeā€™s LemtradaĀ (alemtuzumab), a case report suggests. This unexpected high disease activity raises questions about managing MS through the consecutive use of immunotherapies. The case report, ā€œUnexpected high multiple…

What’s Hot and What’s Not Among MS Therapies?

The newest kids on the MS block, disease-modifying therapies (DMT) such as Genentech’s Ocrevus (ocrelizumab) and Sanofi Genzyme’s Lemtrada (alemtuzumab), are attracting a lot of interest these days. But, some DMTs that have been around for more than two decades are still being prescribed by a lot of neurologists.

FDA Approves Two Bayer Products to Help MS Patients Stay on Top of Interferon Injections

The U.S. Food and Drug Administration has approved a supplemental biologics license application for two BayerĀ products that helpĀ multiple sclerosisĀ patients keep track of their injections ofĀ Betaseron (interferon beta-1b). The products are theĀ myBETAapp and theĀ Betaconnect Navigator software.Ā A biologics license application is a request for permission to market…

FDA Accepts Bayer’s Supplemental BLA for myBETAapp and BETACONNECT Navigator for MS Patients

The U.S. Food and Drug Administration (FDA) has accepted Bayerā€™s filing of a supplemental biologics license application (sBLA) for two products designed to improve the lives of people withĀ multiple sclerosis (MS): myBETAapp and the BETACONNECT Navigator. Bayer created the BETACONNECT systemĀ to increase patient treatment compliance and improve…

#CMSC16 – Interview with Bayer’s VP and General Manager on Betaconnect/Betaseron and Customized Therapy

Global pharmaĀ Bayer HealthcareĀ aims toĀ improve human health by diagnosing, preventing, and treating a variety of diseases. The company currently provides products for general medicine, hematology, neurology, oncology, and women’s healthcare. In 1993, Bayer’s BetaseronĀ (interferon beta-1b) became the first disease-modifying drugĀ to be approved by the U.S. Food and Drug Administration (FDA)Ā for…

FDA Approves BETACONNECT Autoinjector for BETASERON Delivery

Bayer HealthCare is pleased to announce the US Food and Drug Administration (FDA) has granted the approval ofĀ BETACONNECT, a first-of-its-kind electronic autoinjector indicated as a treatment forĀ relapsing-remitting multiple sclerosis (RRMS). For now, theĀ drug delivery device is only compatible with BETASERONĀ®Ā (interferon beta-1b), and will soon be available come early 2016. Ā While…

11-Year Follow-up of Bayer’s BENEFIT Interferon-beta1b Treatment Reveals Positive Results For MS Patients

Results from the BENEFIT11 trial indicate thatĀ early treatment with IFNB-1b leads to improvements inĀ cognition and fatigue in the long-term, as well as sustained employment and favorable magnetic resonance imaging (MRI) outcomes, measured at the 11-year mark. Supported byĀ Bayer HealthCare Pharmaceuticals, the study, titled “Long-term Impact of Early MS Treatment with…

FDA Accepts Bayerā€™s BETACONNECT License Application for Relapsing-Remitting Multiple Sclerosis

Bayer HealthCareĀ recently announced that the U.S. Food and Drug Administration (FDA) has accepted the filing of a supplemental Biologics License Application (sBLA) for BETACONNECT forĀ the treatment of relapsing-remitting multiple sclerosis (MS). BETACONNECT isĀ a new drug delivery option for patients under Bayerā€™s BETASERONĀ® (interferon beta-1b) therapy. MS is a…