Takeda Pharma (TKPYY) 23.1300 $TKPYY
Global Alzheimer's Drugs Market 2014-2018 with Eisai Co. Forest Laboratories, Janssen Pharmaceuticals & Novartis Dominating
M2 - Fri Jul 11, 9:01AM CDT
Research and Markets (http://www.researchandmarkets.com/research/wldkgv/global) has announced the addition of the "Global Alzheimer's Drugs Market 2014-2018" report to their offering. The incidence rates for Alzheimer's disease are increasing, and the global Alzheimer's population is expected to double by 2030. Currently, it is estimated that 5 million Americans suffering from Alzheimer's disease are aged 65 years or above. This number might reach 13.8 million by 2050 as the baby boom generation ages. In the US, Alzheimer's disease is the fifth highest cause factor for deaths among people aged 65 years and above. It has been recognized as the only factor among the top 10 death-causing factors in America for which therapy is not available, preventing or slowing down the progression of disease. The number of deaths resulting from Alzheimer's disease increased by 68 percent during the period of 2000-2010 and this number is expected to increase further during the next decade. In the US, it is estimated that about 7,00,000 people aged 65 years or above will die from Alzheimer's disease in 2014. The incidence rate of Alzheimer's disease is increasing rapidly owing to a rise in the elderly population. In the US, the 2014 incidence rate of Alzheimer's disease for people aged 65 years or above is expected to reach 4,69,000 and this number is expected to double by 2050. According to the report, the Global Alzheimer's Drugs market is driven by several factors, of which the increase in the global aging population is one of the major drivers. The incidence of Alzheimer's disease is growing continuously, mainly because of an increase in the aging population, especially those aged 65 years or above. It is estimated about 596.8 million people will reach 65 years and above in 2014, and this number is expected to reach 681.2 million by 2018. Furthermore, the report states that one of the main challenges is the poor rate of Alzheimer's disease diagnosis. In developed economies, merely 20-50 percent of dementia cases are diagnosed while in developing economies such as India nearly 90 percent cases remain undiagnosed. The lack of diagnosis hampers the effective management of this disease. Key Vendors: - Eisai Co., Ltd. - Forest Laboratories Inc. - Janssen Pharmaceuticals Inc. - Novartis AG Other Prominent Vendors: - Adamas Pharmaceuticals Inc. - Archer Pharmaceuticals Inc. - Eli Lilly and Co. - F. Hoffmann-La Roche Ltd. - FORUM Pharmaceuticals Inc. - H. Lundbeck A/S - Merck & Co., Inc. - MorphoSys AG - Otsuka Pharmaceutical Development & Commercialization Inc./ Otsuka America Pharmaceutical, Inc. - Takeda Pharmaceutical Co., Ltd. - TauRx Pharmaceuticals Ltd. - Zinfandel Pharmaceuticals Inc. Key Topics Covered: - Executive Summary - List of Abbreviations - Scope of the Report - Market Research Methodology - Introduction - Disease Overview - Alzheimer's Disease - Market Landscape - Market Segmentation by MOA - Market Assessment of Top Drugs - Competitive Assessment of Top Drugs - Focus on Alzheimer's Research - Geographical Segmentation - Buying Criteria - Market Growth Drivers - Drivers and their Impact - Market Challenges - Impact of Drivers and Challenges - Market Trends - Trends and their Impact - Vendor Landscape - Future Vendors Expected To Tap the Market - Key Vendor Analysis For more information visit http://www.researchandmarkets.com/research/wldkgv/global
Takeda and Zinfandel Pharmaceuticals to Present Data at Upcoming Alzheimer's Association International Conference® Highlighting Innovative Approaches to Alzheimer's Disease Research and Development
PR Newswire - Thu Jul 10, 8:00AM CDT
Takeda Pharmaceutical Company Limited ("Takeda"
and its partner, Zinfandel Pharmaceuticals, Inc. ("Zinfandel" , will present data during multiple poster and oral sessions at the upcoming Alzheimer's Association International Conference® 2014 (AAIC®), taking place in Copenhagen, Denmark from July 12-17, 2014.
Cognitive Impairment Associated With Schizophrenia (CIAS) Clinical Trials Review, H1, 2014
M2 - Tue Jul 08, 10:48AM CDT
Research and Markets (http://www.researchandmarkets.com/research/85qd7j/cognitive) has announced the addition of the "Cognitive Impairment Associated With Schizophrenia (CIAS) Global Clinical Trials Review, H1, 2014" report to their offering. Cognitive Impairment Associated With Schizophrenia (CIAS) Global Clinical Trials Review, H1, 2014" provides data on the Cognitive Impairment Associated With Schizophrenia (CIAS) clinical trial scenario. This report provides elemental information and data relating to the clinical trials on Cognitive Impairment Associated With Schizophrenia (CIAS). It includes an overview of the trial numbers and their recruitment status as per the site of trial conduction across the globe. The databook offers a preliminary coverage of disease clinical trials by their phase, trial status, prominence of the sponsors and also provides briefing pertaining to the number of trials for the key drugs for treating Cognitive Impairment Associated With Schizophrenia (CIAS). Espy the commercial landscape of the major Universities / Institutes / Hospitals or Companies - Pfizer Inc. - Novartis AG - Merck & Co., Inc. - AbbVie Inc. - Takeda Pharmaceutical Company Limited - Saniona AB - Johnson & Johnson - GlaxoSmithKline plc - VA Greater Los Angeles Healthcare Center - Hamamatsu University School of Medicine - Bronx Veterans Medical Research Foundation - Mashhad University of Medical Sciences - St. Marianna University School of Medicine - Yale University - Indiana University - Central South University - University of Southern Denmark - Northwestern University For more information visit http://www.researchandmarkets.com/research/85qd7j/cognitive
Global Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) Clinical Trials Review, H1, 2014
M2 - Tue Jul 08, 9:47AM CDT
Research and Markets (http://www.researchandmarkets.com/research/n6tm85/chronic) has announced the addition of the "Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) Global Clinical Trials Review, H1, 2014" report to their offering. Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) Global Clinical Trials Review, H1, 2014" provides data on the Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) clinical trial scenario. This report provides elemental information and data relating to the clinical trials on Chronic Inflammatory Demyelinating Polyneuropathy (CIDP). It includes an overview of the trial numbers and their recruitment status as per the site of trial conduction across the globe. The databook offers a preliminary coverage of disease clinical trials by their phase, trial status, prominence of the sponsors and also provides briefing pertaining to the number of trials for the key drugs for treating Chronic Inflammatory Demyelinating Polyneuropathy (CIDP). Espy the commercial landscape of the major Universities / Institutes / Hospitals or Companies - CSL Limited - LFB S.A. - Biogen Idec Inc. - Takeda Pharmaceutical Company Limited - Octapharma AG - Novartis AG - Kedrion S.p.A. - Grifols, S.A. - Grifols Deutschland Gmbh - GeNeuro SA - National Center for Research Resources - Aarhus University - Erasmus MC - State University of New York at Buffalo - Stony Brook University - University of Cologne - Northwestern University - Centre Hospitalier Universitaire de Saint Etienne - Oregon Health and Science University - Rigshospitalet For more information visit http://www.researchandmarkets.com/research/n6tm85/chronic
Phosphodiesterase 4 (PDE-4) Inhibitors Competitor Analysis 2014
M2 - Mon Jun 30, 8:40AM CDT
Research and Markets (http://www.researchandmarkets.com/research/qxlm9z/competitor) has announced the addition of the "Competitor Analysis: Phosphodiesterase 4 (PDE-4) Inhibitors" report to their offering. PDE-4 has become an attractive target for development of oral, inhaled and topical inhibitors for treatment of asthma, chronic obstructive pulmonary disease (COPD), psoriatic arthritis, psoriasis, atopic dermatitis and many more diseases. Purchase of the downloadable pdf report includes a 6-month online access to the data of the report and any updates since the publication date. Credentials to access the database will be sent by e-mail and allow online work with the project data to print or export an individual report. Phosphodiesterase 4 (PDE-4) inhibitors have attracted considerable interest as potential therapeutic agents for inflammatory diseases of the lung, the skin and the gastrointestinal tract, but recently also for diseases of the nervous system. PDE-4 inhibitors are known to reduce elevated cAMP concentrations in inflammatory cells, leading to inhibition of inflammatory response, relaxation of smooth muscle in the airway, and modulation of sensory nerves in the lung as well. Many first and second generation PDE-4 inhibitors have failed in early development due to low therapeutic ratios with nausea and emesis being the main adverse effects. Several PDE-4 inhibitors have advanced to late stage clinical development or even regulatory approval for treatment of COPD and psoriatic arthritis. Other inflammatory diseases for which PDE-4 inhibitors are being evaluated clinically, include psoriasis, atopic dermatitis, rosacea, allergic conjunctivitis, and multiple sclerosis. Age-associated memory impairment and Alzheimer's disease are also studied clinically as indications for PDE-4 inhibitors. The report includes a compilation of currently active projects in research and development of predominantly small molecules specifically or unspecifically inhibiting phosphodiesterase 4 (PDE-4). In addition, the report lists company-specific R&D pipelines of PDE-4 inhibitors. Competitor projects are listed in a tabular format providing information on: - Drug Codes - Target / Mechanism of Action - Class of Compound - Company - Product Category - Indication - R&D Stage and additional comments with a hyperlink leading to the source of information Key Topics Covered: 1. Oral and Inhaled Non-Selective PDE-4 Inhibitors 2. Oral and Inhaled Seletive PDE-4 Inhibitors 3. Topical PDE-4 Inhibitors 4. Corporate PDE-4 Inhibitor R&D Pipelines Companies Mentioned - Alcon (a Novartis company) - Almirall - Anacor Pharmaceuticals - c-a-i-r Biosciences - Celgene - Chiesi Farmaceutici - Dainippon Sumitomo Pharma - Dart NeuroScience - Dermira - Eisai - Forest Laboratories - Gilead Sciences - GlaxoSmithKline - Kyorin Pharmaceutical - Maruho - MediciNova - Merck - Michael J. Fox Foundation - Orchid Chemicals & Pharmaceutical - Otsuka Pharmaceutical - Pharmaxis Sanofi - Takeda Pharmaceutical Co (Nycomed) - Tetra Discovery Partners - Verona Pharma For more information visit http://www.researchandmarkets.com/research/qxlm9z/competitor
Global Hypertension Drugs Market 2014-2018
M2 - Thu Jun 26, 10:22AM CDT
Research and Markets (http://www.researchandmarkets.com/research/tw2n66/global) has announced the addition of the "Global Hypertension Drugs Market 2014-2018" report to their offering. The Global Hypertension Drugs market will grow at a CAGR of 1.2% to 2018 Hypertension, also referred as arterial hypertension or high BP, is a chronic medical condition in which the arterial blood pressure is elevated to an undesired level. Lifestyle habits such as diet, exercising, and smoking are the major causes of hypertension. Hypertension can damage organs and lead to several illnesses such as renal failure, aneurysm, heart failure, stroke, and heart attack. There are two types of hypertension: primary or essential and secondary. The Global Hypertension Drugs market can be categorized into eight segments: - Diuretics - ACE Inhibitors - ARBs - CCB - Beta Blockers - Alpha Blockers - Vasodilators - Renin Inhibitors To calculate the market size, the report considers the revenue generated from the sales of various hypertension drugs used in the treatment of pulmonary arterial hypertension and essential hypertension. The report, the Global Hypertension Drugs Market 2014-2018, has been prepared based on an in-depth market analysis with inputs from industry experts. The report covers the Americas and the EMEA and APAC regions; it also covers the Global Hypertension Drugs market landscape and its growth prospects in the coming years. The report also includes a discussion of the key vendors operating in this market. Key Vendors - Actelion Ltd. - AstraZeneca plc - Boehringer Ingelheim GmbH - Novartis AG - Pfizer Inc. - Sanofi SA Other Prominent Vendors - Bayer AG - Daiichi Sankyo Co. Ltd. - Forest Laboratories Inc. - Merck & Co. Inc. - Takeda Pharmaceutical Co. Ltd. - United Therapeutics Corp. - Valeant Pharmaceuticals International Inc. - XOMA LLC Key Market Drivers/Challenges/Trends - Increase in Aging Population. - Increasing Number of Patent Expirations. - Increasing Focus on Combination Therapies. Key Topics Covered: - Executive Summary - List of Abbreviations - Scope of the Report - Market Research Methodology - Introduction - Market Landscape - Rate of Incidence and Prevalence - Late Stage Pipeline Snapshot - Market Segmentation by Mechanism of Action - Geographical Segmentation - Buying Criteria - Market Growth Drivers - Drivers and their Impact - Market Challenges - Impact of Drivers and Challenges - Market Trends - Trends and their Impact - Vendor Landscape - Key Vendor Analysis For more information visit http://www.researchandmarkets.com/research/tw2n66/global
Takeda Announces Termination of Orteronel (TAK-700) Development for Prostate Cancer in Japan, U.S.A. and Europe
Business Wire - Thu Jun 19, 1:00AM CDT
Takeda Pharmaceutical Company Limited (TSE:4502) announced today that it has voluntarily decided to end the development program for orteronel (TAK-700) for prostate cancer. The decision follows the results of two Phase 3 clinical trials in metastatic, castration resistant prostate cancer (mCRPC). The studies found while orteronel plus prednisone could extend the time patients lived before their cancer progressed, it did not extend overall survival in these patients. After careful consideration of the data from these trials, the company has determined that the drug has not demonstrated a clinical profile sufficient to move forward in mCRPC, given the availability of other therapies.
J&J's Velcade in Focus at the European Hematology Association - Analyst Blog
Zacks Equity Research - Zacks Investment Research - Tue Jun 17, 4:20PM CDT
Johnson & Johnson (JNJ) presented encouraging data from a phase III study on its oncology drug, Velcade, at the annual meeting of the European Hematology Association.
ENTYVIO(TM) (vedolizumab) Now Available in the United States for the Treatment of Adults with Moderately to Severely Active Ulcerative Colitis and Crohn's Disease
PR Newswire - Mon Jun 16, 9:00AM CDT
Takeda Pharmaceutical Company Limited ("Takeda" and its wholly-owned subsidiary, Takeda Pharmaceuticals U.S.A., Inc., today announced the United States (U.S.) commercial availability of a new biologic therapy, ENTYVIO(TM) (vedolizumab), for the treatment of adults with moderately to severely active ulcerative colitis (UC) or Crohn's disease (CD).
New CONNECT Study Presents data on Measures of Cognitive Performance in Adult Patients Treated with Brintellix® (vortioxetine) for Major Depressive Disorder
PR Newswire - Mon Jun 16, 5:30AM CDT
Takeda Pharmaceutical Company Limited (Takeda) and H. Lundbeck A/S (Lundbeck) today announced results from CONNECT, a new study that evaluated the effect of Brintellix 10-20 mg/d on aspects of cognitive function, using an objective neuropsychological test (the Digit Symbol Substitution Test or DSST) associated with executive function, processing speed and attention, in adults with major depressive disorder (MDD). The data will be presented as a late-breaker poster at the 29th International College of Neuropsychopharmacology (CINP) World Congress in Vancouver, Canada.
Affymax terminates Omontys' product collaboration and license agreement with Takeda
M2 - Mon Jun 16, 3:34AM CDT
Biopharmaceutical company Affymax (Other OTC:AFFY) revealed on Friday the termination of its Omontys (peginesatide) product collaboration and license agreement with Takeda Pharmaceutical Company of Osaka, Japan effective 10 September 2014.
Orexigen Slumps as Obesity Drug Approval Delayed - Analyst Blog
Zacks Equity Research - Zacks Investment Research - Thu Jun 12, 5:28PM CDT
Orexigen announced that the FDA has delayed the action date for its obesity candidate, NB32, by three months.
Sepsis - Pipeline Review, H1 2014
M2 - Thu Jun 12, 3:14AM CDT
Research and Markets (http://www.researchandmarkets.com/research/rc2rw6/sepsis_pipeline) has announced the addition of the "Sepsis - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Sepsis, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Sepsis and special features on late-stage and discontinued projects. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products. Scope - The report provides a snapshot of the global therapeutic landscape of Sepsis - The report reviews key pipeline products under drug profile section which includes, product description, MoA and R&D brief, licensing and collaboration details & other developmental activities - The report reviews key players involved in the therapeutics development for Sepsis and enlists all their major and minor projects - The report summarizes all the dormant and discontinued pipeline projects - A review of the Sepsis products under development by companies and universities/research institutes based on information derived from company and industry-specific sources Companies Mentioned: - Baxter International - Daiichi Sankyo Company - Novo Nordisk - Takeda Pharmaceutical Company - Chiesi Farmaceutici - Chong Kun Dang - Eisai - Huons - MetrioPharm - Opsona Therapeutics - Asahi Kasei - MSM Protein Technologies - VG Life Sciences - OncoImmune - Serum Institute of India - Endacea - ISU ABXIS - KAEL-GemVax - biosyn Arzneimittel - Cognosci - Navigen Pharmaceuticals - Lead Discovery Center - Immune Response BioPharma - Novadiscovery - XImmune - Adrenomed - ImmunNovative Developments - Diomune For more information visit http://www.researchandmarkets.com/research/rc...s_pipeline
Helicobacter Pylori Infections - Pipeline Review, H1 2014
M2 - Wed Jun 11, 5:23AM CDT
Research and Markets (http://www.researchandmarkets.com/research/g5smg2/helicobacter) has announced the addition of the "Helicobacter Pylori Infections - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Helicobacter Pylori Infections, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Helicobacter Pylori Infections and special features on late-stage and discontinued projects. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. Reasons to buy - Provides strategically significant competitor information, analysis, and insights to formulate effective R&D development strategies - Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage - Develop strategic initiatives by understanding the focus areas of leading companies - Identify and understand important and diverse types of therapeutics under development for Helicobacter Pylori Infections - Plan mergers and acquisitions effectively by identifying key players of the most promising pipeline - Devise corrective measures for pipeline projects by understanding Helicobacter Pylori Infections pipeline depth and focus of Indication therapeutics - Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope Companies Mentioned: - Sequella, Inc. - Takeda Pharmaceutical Company Limited - Affinium Pharmaceuticals, Ltd. - Microbio Co., Ltd. - MerLion Pharmaceuticals Pte Ltd - ImmunoBiology Ltd. - EpiVax, Inc. - aRigen Pharmaceuticals, Inc. - Vecta Ltd. - Sigmoid Pharma Ltd. - RedHill Biopharma Ltd. For more information visit http://www.researchandmarkets.com/research/g5...licobacter
Takeda Receives European Commission Marketing Authorisation for Entyvio(R) (vedolizumab) for the Treatment of Ulcerative Colitis and Crohn's Disease
PR Newswire Europe - Wed Jun 11, 3:40AM CDT
ZURICH and OSAKA, Japan, May 27, 2014 /PRNewswire/ --
Lupus Nephritis - Pipeline Review, H1 2014
M2 - Tue Jun 10, 3:41AM CDT
Research and Markets (http://www.researchandmarkets.com/research/fdzqtl/lupus_nephritis) has announced the addition of the "Lupus Nephritis - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Lupus Nephritis, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Lupus Nephritis and special features on late-stage and discontinued projects. The report features investigational drugs from across globe covering over 20 therapy areas and nearly 3,000 indications. The report is built using data and information sourced from proprietary databases, Company/University websites, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products. Note*: Certain sections in the report may be removed or altered based on the availability and relevance of data for the indicated disease. Companies Mentioned: - Bristol-Myers Squibb Company - Baxter International Inc. - Johnson & Johnson - Biogen Idec Inc. - GlaxoSmithKline plc - Takeda Pharmaceutical Company Limited - Teva Pharmaceutical Industries Limited - Noxxon Pharma AG - Anthera Pharmaceuticals Inc. - Kadmon Pharmaceuticals, LLC - Azano Pharmaceuticals Inc. For more information visit http://www.researchandmarkets.com/research/fd..._nephritis
Orexigen's Upcoming Pipeline Catalyst - Analyst Blog
Zacks Equity Research - Zacks Investment Research - Mon Jun 09, 3:45PM CDT
The FDA is expected to render a final decision on Orexigen Therapeutics, Inc.'s (OREX) obesity candidate, NB32, by Jun 11.
Global Circadian Rhythm Sleep Disorders Clinical Trials Report 2014
M2 - Fri Jun 06, 4:27AM CDT
Research and Markets (http://www.researchandmarkets.com/research/qkx2tb/circadian_rhythm) has announced the addition of the "Circadian Rhythm Sleep Disorders Global Clinical Trials Review, H1, 2014" report to their offering. Circadian Rhythm Sleep Disorders Global Clinical Trials Review, H1, 2014 provides data on the Circadian Rhythm Sleep Disorders clinical trial scenario. This report provides elemental information and data relating to the clinical trials on Circadian Rhythm Sleep Disorders. It includes an overview of the trial numbers and their recruitment status as per the site of trial conduction across the globe. The databook offers a preliminary coverage of disease clinical trials by their phase, trial status, prominence of the sponsors and also provides briefing pertaining to the number of trials for the key drugs for treating Circadian Rhythm Sleep Disorders. Scope - Data on the number of clinical trials conducted in North America, South and Central America, Europe, Middle-East and Africa and Asia-pacific and top five national contributions in each, along with the clinical trial scenario in BRIC nations - Clinical trial (complete and in progress) data by phase, trial status, subjects recruited and sponsor type - Listings of discontinued trials (suspended, withdrawn and terminated) Espy the commercial landscape of the major Universities / Institutes / Hospitals & Companies - Vanda Pharmaceuticals Inc. - Takeda Pharmaceutical Company Limited - PsyQ - Neurim Pharmaceuticals Ltd - Brigham and Women's Hospital - Oregon Health and Science University - Medical University of Vienna - The University of Chicago - National Institute on Aging - National Eye Institute - Rigshospitalet - University Hospital Basel - Centers for Disease Control and Prevention - Massachusetts General Hospital For more information visit http://www.researchandmarkets.com/research/qk...ian_rhythm
World Smoking Cessation and Nicotine De-addiction Products Market 2013-2019: Nicotine Gums, Patches, Lozenges, Inhalers, Sprays, Sublingual Tablets, Zyban, Chantix/Champix, E-cigarettes
M2 - Wed Jun 04, 3:30AM CDT
Research and Markets (http://www.researchandmarkets.com/research/7ppcf5/smoking_cessation) has announced the addition of the "Smoking Cessation and Nicotine De-addiction Products Market - Global Industry Analysis, Size, Share, Growth, Trends and Forecast, 2013 - 2019" report to their offering. The electronic cigarettes market was valued at USD 1,662.5 million in 2012 and is expected to grow at a CAGR of 33% from 2013 to 2019, to reach an estimated value of USD 12,238.4million in 2019. Key players in the e-cigarettes market include VMR Products LLC, NJOY, Lorillard, Inc., Nicoventures and Altria Group. Electronic cigarettes is the largest and the fastest growing segment in the smoking cessation market. More than 80% of the e-cigarette market share lies with Europe and North America. Regulation of e-cigarettes as medical devices or tobacco products are still in debate. Lobbyists across the globe are trying to influence regulatory agencies to ease restrictions on e-cigarettes. Although this has not yet affected market growth, restrictions and bans on the use of e-cigarettes may adversely affect market growth in the near future. Smoking cessation products are a better alternative for tobacco and cigarette addicts. Smoking cessation products market comprises nicotine replacement therapy (NRT) products, prescription drugs and electronic cigarettes. With the rising incidences of lung cancer, and other diseases such as respiratory and cardiac disorders due to smoking, governments of various countries have started taking initiatives for controlling cigarette addiction. The U.S. Centers for Disease Control and Prevention (CDC) stated that 2011 witnessed around 44 million adults addicted to cigarette smoking in the U.S.,with majority being from the low-income class. Higher taxes on tobacco products, ban on smoking in public places, benefits and assistance for smoking cessation therapies were some of the important policies implemented in order to motivate addicts to quit smoking. Nicotine replacement therapy (NRT) products comprise nicotine gums, patches, lozenges, sprays, inhalers and sublingual tablets. All these products are available over-the-counter, except for Nicotrol nicotine inhalers and nasal sprays which are sold only with prescription. The regulations on sales of NRT products differ from country to country. Nicotine gums are the oldest products in the market and cover around 38% share of the total NRT market. The market for nicotine lozenges is expected to grow at a faster rate owing to convenient use, low cost and easy availability. Nicotine transdermal patches are the second most widely used NRT products for smoking cessation. Major players in the NRT market include GlaxoSmithKline, Novartis and Johnson & Johnson. First line drug therapy for smoking cessation includes Zyban by GlaxoSmithKline, and Chantix (Champix in countries other than the U.S.) by Pfizer. The drug therapy market has suffered from consistent criticism, as suicidal attempts were reported by patients prescribed with either of these drugs. For the same reason, sales of these drugs has been witnessing decline for the past few years. Key Topics Covered: Chapter 1 Introduction Chapter 2 Executive Summary Chapter 3 Global Smoking Cessation and Nicotine De-addiction Market Overview Chapter 4 Global Smoking Cessation and Nicotine De-addiction Products Market, by Product Type Chapter 5 Global Smoking Cessation and Nicotine De-addiction Products Market, by Geography Chapter 6 Competitive Landscape Chapter 7 Recommendations Chapter 8 Company Profiles - Cipla Ltd. - GlaxoSmithKline, Inc. - Imperial Tobacco Company of India (ITC Ltd). - McNeil AB - NJOY, Inc. - Novartis International AG - Pfizer, Inc. - Revolymer PLC - Takeda Pharmaceutical Co. Ltd. - VMR Products LLC For more information visit http://www.researchandmarkets.com/research/7p..._cessation
Poxvirus Infections - Pipeline Review, H1 2014
M2 - Thu May 29, 9:52AM CDT
Research and Markets (http://www.researchandmarkets.com/research/7p3dnk/poxvirus) has announced the addition of the "Poxvirus Infections - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Poxvirus Infections, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Poxvirus Infections and special features on late-stage and discontinued projects. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products. Companies Involved in Therapeutics Development - Takeda Pharmaceutical Company Limited - SIGA Technologies, Inc. - BioApex, s.r.o. For more information visit http://www.researchandmarkets.com/research/7p3dnk/poxvirus
Global Alzheimer's Drugs Market 2014-2018 with Eisai Co. Forest Laboratories, Janssen Pharmaceuticals & Novartis Dominating
M2 - Fri Jul 11, 9:01AM CDT
Research and Markets (http://www.researchandmarkets.com/research/wldkgv/global) has announced the addition of the "Global Alzheimer's Drugs Market 2014-2018" report to their offering. The incidence rates for Alzheimer's disease are increasing, and the global Alzheimer's population is expected to double by 2030. Currently, it is estimated that 5 million Americans suffering from Alzheimer's disease are aged 65 years or above. This number might reach 13.8 million by 2050 as the baby boom generation ages. In the US, Alzheimer's disease is the fifth highest cause factor for deaths among people aged 65 years and above. It has been recognized as the only factor among the top 10 death-causing factors in America for which therapy is not available, preventing or slowing down the progression of disease. The number of deaths resulting from Alzheimer's disease increased by 68 percent during the period of 2000-2010 and this number is expected to increase further during the next decade. In the US, it is estimated that about 7,00,000 people aged 65 years or above will die from Alzheimer's disease in 2014. The incidence rate of Alzheimer's disease is increasing rapidly owing to a rise in the elderly population. In the US, the 2014 incidence rate of Alzheimer's disease for people aged 65 years or above is expected to reach 4,69,000 and this number is expected to double by 2050. According to the report, the Global Alzheimer's Drugs market is driven by several factors, of which the increase in the global aging population is one of the major drivers. The incidence of Alzheimer's disease is growing continuously, mainly because of an increase in the aging population, especially those aged 65 years or above. It is estimated about 596.8 million people will reach 65 years and above in 2014, and this number is expected to reach 681.2 million by 2018. Furthermore, the report states that one of the main challenges is the poor rate of Alzheimer's disease diagnosis. In developed economies, merely 20-50 percent of dementia cases are diagnosed while in developing economies such as India nearly 90 percent cases remain undiagnosed. The lack of diagnosis hampers the effective management of this disease. Key Vendors: - Eisai Co., Ltd. - Forest Laboratories Inc. - Janssen Pharmaceuticals Inc. - Novartis AG Other Prominent Vendors: - Adamas Pharmaceuticals Inc. - Archer Pharmaceuticals Inc. - Eli Lilly and Co. - F. Hoffmann-La Roche Ltd. - FORUM Pharmaceuticals Inc. - H. Lundbeck A/S - Merck & Co., Inc. - MorphoSys AG - Otsuka Pharmaceutical Development & Commercialization Inc./ Otsuka America Pharmaceutical, Inc. - Takeda Pharmaceutical Co., Ltd. - TauRx Pharmaceuticals Ltd. - Zinfandel Pharmaceuticals Inc. Key Topics Covered: - Executive Summary - List of Abbreviations - Scope of the Report - Market Research Methodology - Introduction - Disease Overview - Alzheimer's Disease - Market Landscape - Market Segmentation by MOA - Market Assessment of Top Drugs - Competitive Assessment of Top Drugs - Focus on Alzheimer's Research - Geographical Segmentation - Buying Criteria - Market Growth Drivers - Drivers and their Impact - Market Challenges - Impact of Drivers and Challenges - Market Trends - Trends and their Impact - Vendor Landscape - Future Vendors Expected To Tap the Market - Key Vendor Analysis For more information visit http://www.researchandmarkets.com/research/wldkgv/global
Takeda and Zinfandel Pharmaceuticals to Present Data at Upcoming Alzheimer's Association International Conference® Highlighting Innovative Approaches to Alzheimer's Disease Research and Development
PR Newswire - Thu Jul 10, 8:00AM CDT
Takeda Pharmaceutical Company Limited ("Takeda"
and its partner, Zinfandel Pharmaceuticals, Inc. ("Zinfandel" , will present data during multiple poster and oral sessions at the upcoming Alzheimer's Association International Conference® 2014 (AAIC®), taking place in Copenhagen, Denmark from July 12-17, 2014. Cognitive Impairment Associated With Schizophrenia (CIAS) Clinical Trials Review, H1, 2014
M2 - Tue Jul 08, 10:48AM CDT
Research and Markets (http://www.researchandmarkets.com/research/85qd7j/cognitive) has announced the addition of the "Cognitive Impairment Associated With Schizophrenia (CIAS) Global Clinical Trials Review, H1, 2014" report to their offering. Cognitive Impairment Associated With Schizophrenia (CIAS) Global Clinical Trials Review, H1, 2014" provides data on the Cognitive Impairment Associated With Schizophrenia (CIAS) clinical trial scenario. This report provides elemental information and data relating to the clinical trials on Cognitive Impairment Associated With Schizophrenia (CIAS). It includes an overview of the trial numbers and their recruitment status as per the site of trial conduction across the globe. The databook offers a preliminary coverage of disease clinical trials by their phase, trial status, prominence of the sponsors and also provides briefing pertaining to the number of trials for the key drugs for treating Cognitive Impairment Associated With Schizophrenia (CIAS). Espy the commercial landscape of the major Universities / Institutes / Hospitals or Companies - Pfizer Inc. - Novartis AG - Merck & Co., Inc. - AbbVie Inc. - Takeda Pharmaceutical Company Limited - Saniona AB - Johnson & Johnson - GlaxoSmithKline plc - VA Greater Los Angeles Healthcare Center - Hamamatsu University School of Medicine - Bronx Veterans Medical Research Foundation - Mashhad University of Medical Sciences - St. Marianna University School of Medicine - Yale University - Indiana University - Central South University - University of Southern Denmark - Northwestern University For more information visit http://www.researchandmarkets.com/research/85qd7j/cognitive
Global Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) Clinical Trials Review, H1, 2014
M2 - Tue Jul 08, 9:47AM CDT
Research and Markets (http://www.researchandmarkets.com/research/n6tm85/chronic) has announced the addition of the "Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) Global Clinical Trials Review, H1, 2014" report to their offering. Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) Global Clinical Trials Review, H1, 2014" provides data on the Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) clinical trial scenario. This report provides elemental information and data relating to the clinical trials on Chronic Inflammatory Demyelinating Polyneuropathy (CIDP). It includes an overview of the trial numbers and their recruitment status as per the site of trial conduction across the globe. The databook offers a preliminary coverage of disease clinical trials by their phase, trial status, prominence of the sponsors and also provides briefing pertaining to the number of trials for the key drugs for treating Chronic Inflammatory Demyelinating Polyneuropathy (CIDP). Espy the commercial landscape of the major Universities / Institutes / Hospitals or Companies - CSL Limited - LFB S.A. - Biogen Idec Inc. - Takeda Pharmaceutical Company Limited - Octapharma AG - Novartis AG - Kedrion S.p.A. - Grifols, S.A. - Grifols Deutschland Gmbh - GeNeuro SA - National Center for Research Resources - Aarhus University - Erasmus MC - State University of New York at Buffalo - Stony Brook University - University of Cologne - Northwestern University - Centre Hospitalier Universitaire de Saint Etienne - Oregon Health and Science University - Rigshospitalet For more information visit http://www.researchandmarkets.com/research/n6tm85/chronic
Phosphodiesterase 4 (PDE-4) Inhibitors Competitor Analysis 2014
M2 - Mon Jun 30, 8:40AM CDT
Research and Markets (http://www.researchandmarkets.com/research/qxlm9z/competitor) has announced the addition of the "Competitor Analysis: Phosphodiesterase 4 (PDE-4) Inhibitors" report to their offering. PDE-4 has become an attractive target for development of oral, inhaled and topical inhibitors for treatment of asthma, chronic obstructive pulmonary disease (COPD), psoriatic arthritis, psoriasis, atopic dermatitis and many more diseases. Purchase of the downloadable pdf report includes a 6-month online access to the data of the report and any updates since the publication date. Credentials to access the database will be sent by e-mail and allow online work with the project data to print or export an individual report. Phosphodiesterase 4 (PDE-4) inhibitors have attracted considerable interest as potential therapeutic agents for inflammatory diseases of the lung, the skin and the gastrointestinal tract, but recently also for diseases of the nervous system. PDE-4 inhibitors are known to reduce elevated cAMP concentrations in inflammatory cells, leading to inhibition of inflammatory response, relaxation of smooth muscle in the airway, and modulation of sensory nerves in the lung as well. Many first and second generation PDE-4 inhibitors have failed in early development due to low therapeutic ratios with nausea and emesis being the main adverse effects. Several PDE-4 inhibitors have advanced to late stage clinical development or even regulatory approval for treatment of COPD and psoriatic arthritis. Other inflammatory diseases for which PDE-4 inhibitors are being evaluated clinically, include psoriasis, atopic dermatitis, rosacea, allergic conjunctivitis, and multiple sclerosis. Age-associated memory impairment and Alzheimer's disease are also studied clinically as indications for PDE-4 inhibitors. The report includes a compilation of currently active projects in research and development of predominantly small molecules specifically or unspecifically inhibiting phosphodiesterase 4 (PDE-4). In addition, the report lists company-specific R&D pipelines of PDE-4 inhibitors. Competitor projects are listed in a tabular format providing information on: - Drug Codes - Target / Mechanism of Action - Class of Compound - Company - Product Category - Indication - R&D Stage and additional comments with a hyperlink leading to the source of information Key Topics Covered: 1. Oral and Inhaled Non-Selective PDE-4 Inhibitors 2. Oral and Inhaled Seletive PDE-4 Inhibitors 3. Topical PDE-4 Inhibitors 4. Corporate PDE-4 Inhibitor R&D Pipelines Companies Mentioned - Alcon (a Novartis company) - Almirall - Anacor Pharmaceuticals - c-a-i-r Biosciences - Celgene - Chiesi Farmaceutici - Dainippon Sumitomo Pharma - Dart NeuroScience - Dermira - Eisai - Forest Laboratories - Gilead Sciences - GlaxoSmithKline - Kyorin Pharmaceutical - Maruho - MediciNova - Merck - Michael J. Fox Foundation - Orchid Chemicals & Pharmaceutical - Otsuka Pharmaceutical - Pharmaxis Sanofi - Takeda Pharmaceutical Co (Nycomed) - Tetra Discovery Partners - Verona Pharma For more information visit http://www.researchandmarkets.com/research/qxlm9z/competitor
Global Hypertension Drugs Market 2014-2018
M2 - Thu Jun 26, 10:22AM CDT
Research and Markets (http://www.researchandmarkets.com/research/tw2n66/global) has announced the addition of the "Global Hypertension Drugs Market 2014-2018" report to their offering. The Global Hypertension Drugs market will grow at a CAGR of 1.2% to 2018 Hypertension, also referred as arterial hypertension or high BP, is a chronic medical condition in which the arterial blood pressure is elevated to an undesired level. Lifestyle habits such as diet, exercising, and smoking are the major causes of hypertension. Hypertension can damage organs and lead to several illnesses such as renal failure, aneurysm, heart failure, stroke, and heart attack. There are two types of hypertension: primary or essential and secondary. The Global Hypertension Drugs market can be categorized into eight segments: - Diuretics - ACE Inhibitors - ARBs - CCB - Beta Blockers - Alpha Blockers - Vasodilators - Renin Inhibitors To calculate the market size, the report considers the revenue generated from the sales of various hypertension drugs used in the treatment of pulmonary arterial hypertension and essential hypertension. The report, the Global Hypertension Drugs Market 2014-2018, has been prepared based on an in-depth market analysis with inputs from industry experts. The report covers the Americas and the EMEA and APAC regions; it also covers the Global Hypertension Drugs market landscape and its growth prospects in the coming years. The report also includes a discussion of the key vendors operating in this market. Key Vendors - Actelion Ltd. - AstraZeneca plc - Boehringer Ingelheim GmbH - Novartis AG - Pfizer Inc. - Sanofi SA Other Prominent Vendors - Bayer AG - Daiichi Sankyo Co. Ltd. - Forest Laboratories Inc. - Merck & Co. Inc. - Takeda Pharmaceutical Co. Ltd. - United Therapeutics Corp. - Valeant Pharmaceuticals International Inc. - XOMA LLC Key Market Drivers/Challenges/Trends - Increase in Aging Population. - Increasing Number of Patent Expirations. - Increasing Focus on Combination Therapies. Key Topics Covered: - Executive Summary - List of Abbreviations - Scope of the Report - Market Research Methodology - Introduction - Market Landscape - Rate of Incidence and Prevalence - Late Stage Pipeline Snapshot - Market Segmentation by Mechanism of Action - Geographical Segmentation - Buying Criteria - Market Growth Drivers - Drivers and their Impact - Market Challenges - Impact of Drivers and Challenges - Market Trends - Trends and their Impact - Vendor Landscape - Key Vendor Analysis For more information visit http://www.researchandmarkets.com/research/tw2n66/global
Takeda Announces Termination of Orteronel (TAK-700) Development for Prostate Cancer in Japan, U.S.A. and Europe
Business Wire - Thu Jun 19, 1:00AM CDT
Takeda Pharmaceutical Company Limited (TSE:4502) announced today that it has voluntarily decided to end the development program for orteronel (TAK-700) for prostate cancer. The decision follows the results of two Phase 3 clinical trials in metastatic, castration resistant prostate cancer (mCRPC). The studies found while orteronel plus prednisone could extend the time patients lived before their cancer progressed, it did not extend overall survival in these patients. After careful consideration of the data from these trials, the company has determined that the drug has not demonstrated a clinical profile sufficient to move forward in mCRPC, given the availability of other therapies.
J&J's Velcade in Focus at the European Hematology Association - Analyst Blog
Zacks Equity Research - Zacks Investment Research - Tue Jun 17, 4:20PM CDT
Johnson & Johnson (JNJ) presented encouraging data from a phase III study on its oncology drug, Velcade, at the annual meeting of the European Hematology Association.
ENTYVIO(TM) (vedolizumab) Now Available in the United States for the Treatment of Adults with Moderately to Severely Active Ulcerative Colitis and Crohn's Disease
PR Newswire - Mon Jun 16, 9:00AM CDT
Takeda Pharmaceutical Company Limited ("Takeda"
and its wholly-owned subsidiary, Takeda Pharmaceuticals U.S.A., Inc., today announced the United States (U.S.) commercial availability of a new biologic therapy, ENTYVIO(TM) (vedolizumab), for the treatment of adults with moderately to severely active ulcerative colitis (UC) or Crohn's disease (CD). New CONNECT Study Presents data on Measures of Cognitive Performance in Adult Patients Treated with Brintellix® (vortioxetine) for Major Depressive Disorder
PR Newswire - Mon Jun 16, 5:30AM CDT
Takeda Pharmaceutical Company Limited (Takeda) and H. Lundbeck A/S (Lundbeck) today announced results from CONNECT, a new study that evaluated the effect of Brintellix 10-20 mg/d on aspects of cognitive function, using an objective neuropsychological test (the Digit Symbol Substitution Test or DSST) associated with executive function, processing speed and attention, in adults with major depressive disorder (MDD). The data will be presented as a late-breaker poster at the 29th International College of Neuropsychopharmacology (CINP) World Congress in Vancouver, Canada.
Affymax terminates Omontys' product collaboration and license agreement with Takeda
M2 - Mon Jun 16, 3:34AM CDT
Biopharmaceutical company Affymax (Other OTC:AFFY) revealed on Friday the termination of its Omontys (peginesatide) product collaboration and license agreement with Takeda Pharmaceutical Company of Osaka, Japan effective 10 September 2014.
Orexigen Slumps as Obesity Drug Approval Delayed - Analyst Blog
Zacks Equity Research - Zacks Investment Research - Thu Jun 12, 5:28PM CDT
Orexigen announced that the FDA has delayed the action date for its obesity candidate, NB32, by three months.
Sepsis - Pipeline Review, H1 2014
M2 - Thu Jun 12, 3:14AM CDT
Research and Markets (http://www.researchandmarkets.com/research/rc2rw6/sepsis_pipeline) has announced the addition of the "Sepsis - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Sepsis, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Sepsis and special features on late-stage and discontinued projects. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products. Scope - The report provides a snapshot of the global therapeutic landscape of Sepsis - The report reviews key pipeline products under drug profile section which includes, product description, MoA and R&D brief, licensing and collaboration details & other developmental activities - The report reviews key players involved in the therapeutics development for Sepsis and enlists all their major and minor projects - The report summarizes all the dormant and discontinued pipeline projects - A review of the Sepsis products under development by companies and universities/research institutes based on information derived from company and industry-specific sources Companies Mentioned: - Baxter International - Daiichi Sankyo Company - Novo Nordisk - Takeda Pharmaceutical Company - Chiesi Farmaceutici - Chong Kun Dang - Eisai - Huons - MetrioPharm - Opsona Therapeutics - Asahi Kasei - MSM Protein Technologies - VG Life Sciences - OncoImmune - Serum Institute of India - Endacea - ISU ABXIS - KAEL-GemVax - biosyn Arzneimittel - Cognosci - Navigen Pharmaceuticals - Lead Discovery Center - Immune Response BioPharma - Novadiscovery - XImmune - Adrenomed - ImmunNovative Developments - Diomune For more information visit http://www.researchandmarkets.com/research/rc...s_pipeline
Helicobacter Pylori Infections - Pipeline Review, H1 2014
M2 - Wed Jun 11, 5:23AM CDT
Research and Markets (http://www.researchandmarkets.com/research/g5smg2/helicobacter) has announced the addition of the "Helicobacter Pylori Infections - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Helicobacter Pylori Infections, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Helicobacter Pylori Infections and special features on late-stage and discontinued projects. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. Reasons to buy - Provides strategically significant competitor information, analysis, and insights to formulate effective R&D development strategies - Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage - Develop strategic initiatives by understanding the focus areas of leading companies - Identify and understand important and diverse types of therapeutics under development for Helicobacter Pylori Infections - Plan mergers and acquisitions effectively by identifying key players of the most promising pipeline - Devise corrective measures for pipeline projects by understanding Helicobacter Pylori Infections pipeline depth and focus of Indication therapeutics - Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope Companies Mentioned: - Sequella, Inc. - Takeda Pharmaceutical Company Limited - Affinium Pharmaceuticals, Ltd. - Microbio Co., Ltd. - MerLion Pharmaceuticals Pte Ltd - ImmunoBiology Ltd. - EpiVax, Inc. - aRigen Pharmaceuticals, Inc. - Vecta Ltd. - Sigmoid Pharma Ltd. - RedHill Biopharma Ltd. For more information visit http://www.researchandmarkets.com/research/g5...licobacter
Takeda Receives European Commission Marketing Authorisation for Entyvio(R) (vedolizumab) for the Treatment of Ulcerative Colitis and Crohn's Disease
PR Newswire Europe - Wed Jun 11, 3:40AM CDT
ZURICH and OSAKA, Japan, May 27, 2014 /PRNewswire/ --
Lupus Nephritis - Pipeline Review, H1 2014
M2 - Tue Jun 10, 3:41AM CDT
Research and Markets (http://www.researchandmarkets.com/research/fdzqtl/lupus_nephritis) has announced the addition of the "Lupus Nephritis - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Lupus Nephritis, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Lupus Nephritis and special features on late-stage and discontinued projects. The report features investigational drugs from across globe covering over 20 therapy areas and nearly 3,000 indications. The report is built using data and information sourced from proprietary databases, Company/University websites, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products. Note*: Certain sections in the report may be removed or altered based on the availability and relevance of data for the indicated disease. Companies Mentioned: - Bristol-Myers Squibb Company - Baxter International Inc. - Johnson & Johnson - Biogen Idec Inc. - GlaxoSmithKline plc - Takeda Pharmaceutical Company Limited - Teva Pharmaceutical Industries Limited - Noxxon Pharma AG - Anthera Pharmaceuticals Inc. - Kadmon Pharmaceuticals, LLC - Azano Pharmaceuticals Inc. For more information visit http://www.researchandmarkets.com/research/fd..._nephritis
Orexigen's Upcoming Pipeline Catalyst - Analyst Blog
Zacks Equity Research - Zacks Investment Research - Mon Jun 09, 3:45PM CDT
The FDA is expected to render a final decision on Orexigen Therapeutics, Inc.'s (OREX) obesity candidate, NB32, by Jun 11.
Global Circadian Rhythm Sleep Disorders Clinical Trials Report 2014
M2 - Fri Jun 06, 4:27AM CDT
Research and Markets (http://www.researchandmarkets.com/research/qkx2tb/circadian_rhythm) has announced the addition of the "Circadian Rhythm Sleep Disorders Global Clinical Trials Review, H1, 2014" report to their offering. Circadian Rhythm Sleep Disorders Global Clinical Trials Review, H1, 2014 provides data on the Circadian Rhythm Sleep Disorders clinical trial scenario. This report provides elemental information and data relating to the clinical trials on Circadian Rhythm Sleep Disorders. It includes an overview of the trial numbers and their recruitment status as per the site of trial conduction across the globe. The databook offers a preliminary coverage of disease clinical trials by their phase, trial status, prominence of the sponsors and also provides briefing pertaining to the number of trials for the key drugs for treating Circadian Rhythm Sleep Disorders. Scope - Data on the number of clinical trials conducted in North America, South and Central America, Europe, Middle-East and Africa and Asia-pacific and top five national contributions in each, along with the clinical trial scenario in BRIC nations - Clinical trial (complete and in progress) data by phase, trial status, subjects recruited and sponsor type - Listings of discontinued trials (suspended, withdrawn and terminated) Espy the commercial landscape of the major Universities / Institutes / Hospitals & Companies - Vanda Pharmaceuticals Inc. - Takeda Pharmaceutical Company Limited - PsyQ - Neurim Pharmaceuticals Ltd - Brigham and Women's Hospital - Oregon Health and Science University - Medical University of Vienna - The University of Chicago - National Institute on Aging - National Eye Institute - Rigshospitalet - University Hospital Basel - Centers for Disease Control and Prevention - Massachusetts General Hospital For more information visit http://www.researchandmarkets.com/research/qk...ian_rhythm
World Smoking Cessation and Nicotine De-addiction Products Market 2013-2019: Nicotine Gums, Patches, Lozenges, Inhalers, Sprays, Sublingual Tablets, Zyban, Chantix/Champix, E-cigarettes
M2 - Wed Jun 04, 3:30AM CDT
Research and Markets (http://www.researchandmarkets.com/research/7ppcf5/smoking_cessation) has announced the addition of the "Smoking Cessation and Nicotine De-addiction Products Market - Global Industry Analysis, Size, Share, Growth, Trends and Forecast, 2013 - 2019" report to their offering. The electronic cigarettes market was valued at USD 1,662.5 million in 2012 and is expected to grow at a CAGR of 33% from 2013 to 2019, to reach an estimated value of USD 12,238.4million in 2019. Key players in the e-cigarettes market include VMR Products LLC, NJOY, Lorillard, Inc., Nicoventures and Altria Group. Electronic cigarettes is the largest and the fastest growing segment in the smoking cessation market. More than 80% of the e-cigarette market share lies with Europe and North America. Regulation of e-cigarettes as medical devices or tobacco products are still in debate. Lobbyists across the globe are trying to influence regulatory agencies to ease restrictions on e-cigarettes. Although this has not yet affected market growth, restrictions and bans on the use of e-cigarettes may adversely affect market growth in the near future. Smoking cessation products are a better alternative for tobacco and cigarette addicts. Smoking cessation products market comprises nicotine replacement therapy (NRT) products, prescription drugs and electronic cigarettes. With the rising incidences of lung cancer, and other diseases such as respiratory and cardiac disorders due to smoking, governments of various countries have started taking initiatives for controlling cigarette addiction. The U.S. Centers for Disease Control and Prevention (CDC) stated that 2011 witnessed around 44 million adults addicted to cigarette smoking in the U.S.,with majority being from the low-income class. Higher taxes on tobacco products, ban on smoking in public places, benefits and assistance for smoking cessation therapies were some of the important policies implemented in order to motivate addicts to quit smoking. Nicotine replacement therapy (NRT) products comprise nicotine gums, patches, lozenges, sprays, inhalers and sublingual tablets. All these products are available over-the-counter, except for Nicotrol nicotine inhalers and nasal sprays which are sold only with prescription. The regulations on sales of NRT products differ from country to country. Nicotine gums are the oldest products in the market and cover around 38% share of the total NRT market. The market for nicotine lozenges is expected to grow at a faster rate owing to convenient use, low cost and easy availability. Nicotine transdermal patches are the second most widely used NRT products for smoking cessation. Major players in the NRT market include GlaxoSmithKline, Novartis and Johnson & Johnson. First line drug therapy for smoking cessation includes Zyban by GlaxoSmithKline, and Chantix (Champix in countries other than the U.S.) by Pfizer. The drug therapy market has suffered from consistent criticism, as suicidal attempts were reported by patients prescribed with either of these drugs. For the same reason, sales of these drugs has been witnessing decline for the past few years. Key Topics Covered: Chapter 1 Introduction Chapter 2 Executive Summary Chapter 3 Global Smoking Cessation and Nicotine De-addiction Market Overview Chapter 4 Global Smoking Cessation and Nicotine De-addiction Products Market, by Product Type Chapter 5 Global Smoking Cessation and Nicotine De-addiction Products Market, by Geography Chapter 6 Competitive Landscape Chapter 7 Recommendations Chapter 8 Company Profiles - Cipla Ltd. - GlaxoSmithKline, Inc. - Imperial Tobacco Company of India (ITC Ltd). - McNeil AB - NJOY, Inc. - Novartis International AG - Pfizer, Inc. - Revolymer PLC - Takeda Pharmaceutical Co. Ltd. - VMR Products LLC For more information visit http://www.researchandmarkets.com/research/7p..._cessation
Poxvirus Infections - Pipeline Review, H1 2014
M2 - Thu May 29, 9:52AM CDT
Research and Markets (http://www.researchandmarkets.com/research/7p3dnk/poxvirus) has announced the addition of the "Poxvirus Infections - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Poxvirus Infections, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Poxvirus Infections and special features on late-stage and discontinued projects. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products. Companies Involved in Therapeutics Development - Takeda Pharmaceutical Company Limited - SIGA Technologies, Inc. - BioApex, s.r.o. For more information visit http://www.researchandmarkets.com/research/7p3dnk/poxvirus
