EMD Serono Highlights Scientific Commitment to MS with Data Presented at the AAN Annual Meeting
- Data analyses in relapsing MS highlight MRI outcomes and 'no evident disease activity' (NEDA) measure for Rebif® (interferon beta-1a) vs. Avonex® (interferon beta-1a)
ROCKLAND, Mass., April 16, 2015 /PRNewswire/ -- EMD Serono, the U.S. biopharmaceuticals business of Merck KGaA, Darmstadt, Germany, announced today that data about Rebif® (interferon beta-1a), the company's high-dose, high-frequency interferon for relapsing forms of multiple sclerosis, will be presented at the American Academy of Neurology's 67th Annual Meeting, taking place from April 18 - 25, in Washington, D.C.
Data from 13 abstracts to be presented at AAN assess the clinical effect of Rebif on NEDA and MRI outcomes, among other measures. The data also explore trends in treatment adherence among patients treated with self-injectables versus oral therapies, and barriers to adherence in those living with MS.
"EMD Serono is focused on optimizing care for people living with MS, and part of this commitment involves continuing to analyze the efficacy, safety and real-world use of Rebif," said Dr. Rick Munschauer, Vice President, Medical Affairs, Neurology and Immunology, EMD Serono. "These data presented at AAN continue to advance our understanding of the important clinical effects of Rebif."
In addition to Rebif, EMD Serono is engaged in strategic research collaborations funding promising neurology research with leading academic and healthcare institutions. The company also has ongoing MS clinical study programs, including a Phase I study of ATX-MS-1467, an investigational therapy for relapsing remitting multiple sclerosis (RRMS), and a Phase IIb study of imilecleucel-T, an investigational therapy for Secondary Progressive MS (SPMS), an area of high unmet medical need. The company has an option agreement with Opexa Therapeutics, Inc. for the development and commercial licensing of imilecleucel-T.
The following abstracts have been accepted for presentation at the 67th AAN Annual Meeting:
Title |
Lead author |
Abstract/ |
Presentation date/time (CDT) |
Session |
Room/ |
Effect of Age and Sex on Cost of Multiple Sclerosis–Related Relapse Defined by Inpatient Stays |
Chris M. Kozma |
P1.136 |
April 20, 2015 |
Poster Session I: MS and CNS Inflammatory Diseases: Symptoms, Specific Symptomatic Treatment, Co-morbidities, and Costs (2:00-6:30 pm) |
Hall E
|
Quality of Life Perceptions Correlate with Longitudinal Clinical Relapse Reduction Metrics in Patients Treated with Subcutaneous Interferon beta-1a Given Three Times a Week (collaboration with New York State MS Consortium (NYSMSC) |
Barbara Teter |
P1.113 |
April 20, 2015 |
Poster Session I: Neuroepidemiology: MS and CNS Inflammatory Diseases (2:00-6:30 pm) |
Hall E
|
Relationship between Cognitive Status and Perception of Ease of Use of an Electronic Autoinjector for Subcutaneous Interferon Beta-1a |
Ajay Gupta |
P3.225 |
April 21, 2015 |
Poster Session III: MS and CNS Inflammatory Diseases: Tools for Clinical Assessment and Therapeutic Response (2:00-6:30 pm) |
Hall E
|
Post-Marketing Safety Profile of Interferon beta-1a SC in Patients with Multiple Sclerosis Treated in the US: a Retrospective Cohort Study |
Meredith Y. Smith |
P3.268 |
April 21, 2015 |
Poster Session III: MS and CNS Inflammatory Diseases: Treatment Efficacy, Safety and Tolerability (2:00-6:30 pm) |
Hall E
|
An Assessment of Adherence Among MS Patients Newly Initiating Treatment with a Self-injectable vs Oral Disease-Modifying Drug |
Julie C. Locklear |
P3.281 |
April 21 2015, |
Poster Session III: MS and CNS Inflammatory Diseases: Treatment Efficacy, Safety and Tolerability (2:00-6:30 pm) |
Hall E
|
A Pragmatic Literature Review of Network Meta-Analyses of Disease-Modifying Drugs in the Treatment of MS |
Amy Phillips |
P3.232 |
April 21, 2015 |
Poster Session III: MS and CNS Inflammatory Diseases: Tools for Clinical Assessment and Therapeutic Response (2:00-6:30 pm) |
Hall E
|
An Exploratory Analysis of Predictors of Disease-Modifying Drug Adherence Using Data from a Panel Survey of Patients with Multiple Sclerosis |
Julie C.Locklear |
P3.217 |
April 21, 2015 2:00 pm |
Poster Session III: MS and CNS Inflammatory Diseases: Tools for Clinical Assessment and Therapeutic Response (2:00-6:30 pm) |
Hall E
|
Early Effects of Interferon beta-1a SC tiw Versus Interferon beta-1a IM qw on MRI Outcomes in Patients with Relapsing MS in the EVIDENCE Study |
Anthony T. Reder |
P7.257 |
April 23, 2015 |
Poster Session VII: MS and CNS Inflammatory Diseases: Clinical Trials (2:00-6:30 pm) |
Hall E
|
No Evidence of Disease Activity in Patients with Relapsing MS Treated with Interferon beta-1a SC tiw Versus Interferon beta-1a IM qw in the EVIDENCE Study |
Patricia Coyle
|
P7.220 |
April 23, 2015 |
Poster Session VII: MS and CNS Inflammatory Diseases: Clinical Trials (2:00-6:30 pm) |
Hall E
|
No Evidence of Disease Activity in Patients with Relapsing MS Treated with Interferon Beta-1a SC tiw versus Interferon Beta-1a IM qw: Subgroup Analyses of the EVIDENCE Study |
Juanzhi Fang |
P7.271 |
April 23, 2015 |
Poster Session VII: MS and CNS Inflammatory Diseases: Clinical Trials (2:00-6:30 pm) |
Hall E
|
1-Year Efficacy and Tolerability Results for IFN beta-1a SC tiw Treatment and Predictive Value of 6-Month MRI: Exploratory Analysis of PRISMS Data in Patients with RRMS |
Mark Cascione |
P7.242 |
April 23, 2015 |
Poster Session VII: MS and CNS Inflammatory Diseases: Clinical Trials (2:00-6:30 pm) |
Hall E
|
Early Onset and Predictive Value of MRI Measures Among Patients Receiving Interferon beta-1a SC tiw for RRMS: Post Hoc Analyses of PRISMS-2 Data |
David Li |
P7.254 |
April 23, 2015 |
Poster Session VII: MS and CNS Inflammatory Diseases: Clinical Trials (2:00-6:30 pm) |
Hall E
|
Development of Chronic Black Holes (CBH) Predicts Long Term Disability: Post-Hoc Analysis of Magnetic Resonance Imaging (MRI) Data in the PRISMS Study (collaboration with Merck Serono, Global Medical) |
Tony Traboulsee |
P7.251 |
April 23, 2015 |
Poster Session VII: MS and CNS Inflammatory Diseases: Clinical Trials (2:00-6:30 pm) |
Hall E
|
Learn more about EMD Serono's programs, pipeline and activities in neurology by visiting our booth at this year's AAN Annual Meeting.
Avonex® (interferon beta-1a) is a registered trademark of Biogen Inc.
About Rebif® (interferon beta-1a)
Rebif (interferon beta-1a) is used to treat relapsing forms of MS to decrease the frequency of relapses and delay the occurrence of some of the physical disability that is common in people with MS.
Important Safety Information
Before beginning treatment, you should discuss the potential benefits and risks associated with Rebif with your healthcare provider.
Rebif can cause serious side effects. Tell your healthcare provider right away if you have any of the symptoms listed below while taking Rebif.
- Behavioral health problems including depression and suicidal thoughts. You may have mood problems including depression (feeling hopeless or feeling bad about yourself), and thoughts of hurting yourself or suicide
- Liver problems or worsening of liver problems including liver failure. Symptoms may include nausea, loss of appetite, tiredness, dark colored urine and pale stools, yellowing of your skin or the white part of your eye, bleeding more easily than normal, confusion, and sleepiness. During your treatment with Rebif you will need to see your healthcare provider regularly and have regular blood tests to check for side effects
- Serious allergic and skin reactions. Symptoms may include itching, swelling of your face, eyes, lips, tongue or throat, trouble breathing, anxiousness, feeling faint, skin rash, hives, sores in your mouth, or skin blisters and peels
- Injection site problems. Symptoms at the injection site may include redness, pain, swelling, color changes (blue or black), and drainage of fluid.
- Blood problems. Rebif can affect your bone marrow and cause low red and white blood cell, and platelet counts. In some people, these blood cell counts may fall to dangerously low levels. If your blood cell counts become very low, you can get infections and problems with bleeding and bruising. Your healthcare provider may ask you to have regular blood tests to check for blood problems
- Seizures. Some people have had seizures while taking Rebif
Rebif will not cure your MS but may decrease the number of flare-ups of the disease and slow the occurrence of some of the physical disability that is common in people with MS.
Do not take Rebif if you are allergic to interferon beta, human albumin, or any of the ingredients in Rebif.
Before you take Rebif, tell your healthcare provider if you have or have had any of the following conditions:
- mental illness, including depression and suicidal behavior
- liver problems, bleeding problems or blood clots, low blood cell counts, seizures (epilepsy), or thyroid problems
- drink alcohol
- you are pregnant or plan to become pregnant. It is not known if Rebif will harm your unborn baby. Tell your healthcare provider if you become pregnant during your treatment with Rebif.
- you are breastfeeding or plan to breastfeed. It is not known if Rebif passes into your breast milk. You and your healthcare provider should decide if you will use Rebif or breastfeed. You should not do both.
Tell your healthcare provider about all medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements.
The most common side effects of Rebif include:
- flu-like symptoms. You may have flu-like symptoms when you first start taking Rebif. You may be able to manage these flu-like symptoms by taking over-the-counter pain and fever reducers. For many people, these symptoms lessen or go away over time. Symptoms may include muscle aches, fever, tiredness, and chills
- stomach pain
- change in liver blood tests
For additional information about Rebif, please consult the Prescribing Information and Medication Guide at www.rebif.com and talk to a health care professional.
About EMD Serono
EMD Serono, a subsidiary of Merck KGaA, Darmstadt, Germany, is a leading US biopharmceutical company focused exclusively on specialty care. For more than 40 years, EMD Serono has integrated cutting-edge science, innovative products and devices, and industry-leading patient support and access programs. EMD Serono has deep expertise in neurology, fertility and endocrinology, as well as a robust pipeline of potential therapies in neurology, oncology, immunology and immunooncology. Today, EMD Serono has more than 1,100 employees around the country with commercial, clinical and research operations based in the company's home state of Massachusetts.
For more information, please visit www.emdserono.com
About Merck KGaA, Darmstadt, Germany
Merck KGaA of Darmstadt, Germany, is a leading company for innovative and top-quality high-tech products in healthcare, life science and performance materials. The company has six businesses – Biopharmaceuticals, Consumer Health, Allergopharma, Biosimilars, Life Science and Performance Materials – and generated sales of € 11.3 billion in 2014. Around 39,000 employees work in 66 countries to improve the quality of life for patients, to foster the success of customers and to help meet global challenges. Merck KGaA, Darmstadt, Germany, is the world's oldest pharmaceutical and chemical company – since 1668, the company has stood for innovation, business success and responsible entrepreneurship. Holding an approximately 70% interest, the founding family remains the majority owner of the company to this day. Merck KGaA, Darmstadt, Germany holds the global rights to the Merck name and brand. The only exceptions are Canada and the United States, where the company operates as EMD Serono, EMD Millipore and EMD Performance Materials.
Erin Marie Beals
Phone 781-681-2850
Logo - http://photos.prnewswire.com/prnh/20140902/141783
SOURCE EMD Serono
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