{"id":2569,"date":"2020-10-30T00:00:00","date_gmt":"2021-03-18T00:54:07","guid":{"rendered":"https:\/\/www.9-design.net\/?p=2569"},"modified":"2021-03-18T08:54:07","modified_gmt":"2021-03-18T00:54:07","slug":"european-medicines-agency-accepts-biogens-aducanumab-marketing-authorization-application-for-alzheimers-disease","status":"publish","type":"post","link":"https:\/\/www.9-design.net\/en\/2020\/10\/30\/european-medicines-agency-accepts-biogens-aducanumab-marketing-authorization-application-for-alzheimers-disease\/","title":{"rendered":"European Medicines Agency Accepts Biogen\u2019s Aducanumab Marketing Authorization Application for Alzheimer\u2019s Disease"},"content":{"rendered":"

If approved, aducanumab would become the first therapy to reduce the clinical decline of Alzheimer\u2019s disease and to meaningfully change the course of Alzheimer\u2019s disease<\/em><\/span><\/p>\n

Biogen (Nasdaq: BIIB) and Eisai, Co., Ltd. (Tokyo, Japan) today announced that the European Medicines Agency (EMA) has confirmed it has accepted for review, following a standard timetable, the Marketing Authorization Application (MAA) for aducanumab, an investigational treatment for Alzheimer\u2019s disease. Clinical data from patients with Mild Cognitive Impairment due to Alzheimer\u2019s disease and mild Alzheimer\u2019s disease demonstrate that treatment with aducanumab resulted in the removal of amyloid beta and better clinical outcomes. If approved, aducanumab would become the first therapy to reduce the clinical decline in patients with Alzheimer\u2019s disease.<\/p>\n

\u201cAlzheimer\u2019s disease has become a significant and growing burden for societies around the world, and we believe aducanumab represents the first breakthrough that can change the course of this devastating disease,\u201d said Michel Vounatsos, Chief Executive Officer at Biogen. \u201cWe are committed to working with regulatory authorities worldwide and we look forward to the European Medicines Agency\u2019s review of this application.\u201d<\/p>\n

\u201cThere are no treatments available that impact the progression of Alzheimer\u2019s disease by addressing the underlying disease pathology. The potential that aducanumab may hold to effectively reduce the clinical decline brings new hope to people and families living with this devastating disease,\u201d said Dr. Haruo Naito, Chief Executive Officer at Eisai Co., Ltd. \u201cThe acceptance of the Marketing Authorization Application in the European Union is an important milestone as we work towards making this potential treatment available around the world.\u201d<\/p>\n

Aducanumab is also under review with the U.S. Food and Drug Administration with Priority Review, with a Prescription Drug User Fee Act (PDUFA) action date of March 7, 2021.<\/p>\n

 <\/p>\n

About Aducanumab<\/b><\/p>\n

Aducanumab (BIIB037) is an investigational human monoclonal antibody studied for the treatment of Alzheimer\u2019s disease. Based on clinical data from patients with Mild Cognitive Impairment due to Alzheimer\u2019s disease and mild Alzheimer\u2019s disease, aducanumab has the potential to impact underlying disease pathophysiology, slow cognitive and functional decline and provide benefits on patients\u2019 ability to perform activities of daily living, including conducting personal finances, performing household chores, such as cleaning, shopping and doing laundry, and independently traveling out of the home. If approved, aducanumab would be the first treatment to meaningfully change the course of the disease for individuals living with Alzheimer\u2019s.<\/p>\n

Biogen licensed aducanumab from Neurimmune under a collaborative development and license agreement. Since October 2017 Biogen and Eisai Co., Ltd. have collaborated on the development and commercialization of aducanumab globally.<\/p>\n

EMERGE and ENGAGE were Phase 3 multicenter, randomized, double-blind, placebo-controlled, parallel-group studies designed to evaluate the efficacy and safety of aducanumab. The primary objective of the studies was to evaluate the efficacy of monthly doses of aducanumab as compared with placebo in reducing cognitive and functional impairment as measured by changes in the Clinical Dementia Rating-Sum of Boxes (CDR-SB) score. Secondary objectives were to assess the effect of monthly doses of aducanumab as compared to placebo on clinical decline as measured by the Mini-Mental State Examination (MMSE), Alzheimer\u2019s Disease Assessment Scale-Cognitive Subscale 13 Items (ADAS-Cog 13) and Alzheimer\u2019s Disease Cooperative Study-Activities of Daily Living Inventory Mild Cognitive Impairment Version (ADCS-ADL-MCI).<\/p>\n

 <\/p>\n

About Alzheimer\u2019s Disease<\/b><\/p>\n

Alzheimer\u2019s disease is a progressive neurological condition that impairs thinking, memory and independence, leading to premature death. The disease currently cannot be stopped, delayed or prevented and is a growing global health crisis, affecting those living with the disease and their families. According to the World Health Organization (WHO), tens of millions of people worldwide live with Alzheimer\u2019s disease, and the number will grow in the years ahead, outpacing the healthcare resources needed to manage it and costing billions of dollars.<\/p>\n

The Alzheimer\u2019s Disease International 2019 Alzheimer\u2019s Yearbook estimates that approximately 10 million people in the EU suffer from dementia (excluding Mild Cognitive Impairment). AD is suspected to represent around 60-70% of dementia cases.<\/p>\n

Alzheimer\u2019s disease is characterized by changes in the brain, including the abnormal accumulation of toxic amyloid beta plaque, which begins approximately 20 years before patients exhibit symptoms of the disease. Mild Cognitive Impairment due to Alzheimer\u2019s disease is one of the earliest stages of the disease when symptoms start to be more visible and can be detected and diagnosed. Current research efforts are focused on catching and treating patients as early as possible for the best chance of slowing or stopping the progression of Alzheimer\u2019s disease.<\/p>\n

\u00a0\u00a0<\/b><\/p>\n

About Biogen<\/b><\/p>\n

At Biogen, our mission is clear: we are pioneers in neuroscience. Biogen discovers, develops and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases as well as related therapeutic adjacencies. One of the world\u2019s first global biotechnology companies, Biogen was founded in 1978 by Charles Weissmann, Heinz Schaller, Kenneth Murray and Nobel Prize winners Walter Gilbert and Phillip Sharp. Today Biogen has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first approved treatment for spinal muscular atrophy, commercializes biosimilars of advanced biologics and is focused on advancing research programs in multiple sclerosis and neuroimmunology, Alzheimer\u2019s disease and dementia, neuromuscular disorders, movement disorders, ophthalmology, immunology, neurocognitive disorders, acute neurology and pain.<\/p>\n

We routinely post information that may be important to investors on our website at\u00a0www.biogen.com<\/a>. Follow us on social media \u2013\u00a0Twitter<\/a>,\u00a0LinkedIn<\/a>,\u00a0Facebook<\/a>,\u00a0YouTube<\/a>.<\/p>\n

\u00a0\u00a0<\/b><\/p>\n

About Eisai Co., Ltd.<\/b><\/p>\n

Eisai Co., Ltd. is a leading global pharmaceutical company headquartered in Japan. Eisai\u2019s corporate philosophy is based on the\u00a0human health care (hhc)\u00a0<\/i>concept, which is to give first thought to patients and their families, and to increase the benefits that health care provides to them. With a global network of R&D facilities, manufacturing sites and marketing subsidiaries, we strive to realize our\u00a0hhc<\/i>\u00a0philosophy by delivering innovative products to target diseases with high unmet medical needs, with a particular focus in our strategic areas of Neurology and Oncology.<\/p>\n

Leveraging the experience gained from the development and marketing a treatment for Alzheimer\u2019s disease, Eisai aims to establish the \u201cEisai Dementia Platform.\u201d Through this platform, Eisai plans to deliver novel benefits to those living with dementia and their families through constructing a \u201cDementia Ecosystem,\u201d by collaborating with partners such as medical organizations, diagnostic development companies, research organizations, and bio-ventures in addition to private insurance agencies, finance industries, fitness clubs, automobile makers, retailers, and care facilities. For more information about Eisai Co., Ltd., please visit\u00a0https:\/\/www.eisai.com<\/a>.<\/p>\n

 <\/p>\n

Biogen Safe Harbor\u00a0<\/b><\/p>\n

This news release contains forward-looking statements, including statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, about potential regulatory discussions, submissions and approvals and the timing thereof; the potential clinical effects of aducanumab; the potential benefits, safety and efficacy of aducanumab; the treatment of Alzheimer\u2019s disease; the anticipated benefits and potential of Biogen\u2019s collaboration arrangements with Eisai; the potential of Biogen\u2019s commercial business and pipeline programs, including aducanumab; and risks and uncertainties associated with drug development and commercialization. These statements may be identified by words such as \u201caim,\u201d \u201canticipate,\u201d \u201cbelieve,\u201d \u201ccould,\u201d \u201cestimate,\u201d \u201cexpect,\u201d \u201cforecast,\u201d \u201cintend,\u201d \u201cmay,\u201d \u201cplan,\u201d \u201cpossible,\u201d \u201cpotential,\u201d \u201cwill,\u201d \u201cwould\u201d and other words and terms of similar meaning. Drug development and commercialization involve a high degree of risk, and only a small number of research and development programs result in commercialization of a product. Results in early stage clinical trials may not be indicative of full results or results from later stage or larger scale clinical trials and do not ensure regulatory approval. You should not place undue reliance on these statements or the scientific data presented.<\/p>\n

These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements, including without limitation actual timing and content of submissions to and decisions made by the regulatory authorities regarding aducanumab; regulatory submissions may take longer or be more difficult to complete than expected; regulatory authorities may require additional information or further studies, or may fail or refuse to approve or may delay approval of Biogen\u2019s drug candidates, including aducanumab; unexpected concerns that may arise from additional data, analysis or results obtained during clinical trials; the occurrence of adverse safety events; risks of unexpected costs or delays; the risk of other unexpected hurdles; uncertainty of success in the development and potential commercialization of aducanumab; risks relating to the potential launch of aducanumab, including preparedness of healthcare providers to treat patients, the ability to obtain and maintain adequate reimbursement for aducanumab and other unexpected difficulties or hurdles; failure to protect and enforce Biogen\u2019s data, intellectual property and other proprietary rights and uncertainties relating to intellectual property claims and challenges; product liability claims; third party collaboration risks; and the direct and indirect impacts of the ongoing COVID-19 pandemic on Biogen\u2019s business, results of operations and financial condition. The foregoing sets forth many, but not all, of the factors that could cause actual results to differ from Biogen\u2019s expectations in any forward-looking statement. Investors should consider this cautionary statement, as well as the risk factors identified in Biogen\u2019s most recent annual or quarterly report and in other reports Biogen has filed with the U.S. Securities and Exchange Commission. These statements are based on Biogen\u2019s current beliefs and expectations and speak only as of the date of this news release. Biogen does not undertake any obligation to publicly update any forward-looking statements, whether as a result of new information, future developments or otherwise.<\/p>\n","protected":false},"excerpt":{"rendered":"

If approved, aducanumab would become the first therapy to reduce the clinical decline of Alzheimer\u2019s disease and to meaningfully change the course of Alzheimer\u2019s disease<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[28],"tags":[],"_links":{"self":[{"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/posts\/2569"}],"collection":[{"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/comments?post=2569"}],"version-history":[{"count":2,"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/posts\/2569\/revisions"}],"predecessor-version":[{"id":2571,"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/posts\/2569\/revisions\/2571"}],"wp:attachment":[{"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/media?parent=2569"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/categories?post=2569"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.9-design.net\/wp-json\/wp\/v2\/tags?post=2569"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}久久人人97超碰超国产,天天摸夜夜添夜夜无码,久久精品人人槡人妻人人玩,97碰碰碰人妻无码视频