LSIS Feed - Johnson & Johnson from 05.02.2012This is the RSS news feed of one of our preset news channels on LSIS - The Life Science Infromation Service. Please visit us to find a current view of this one and many more channels via our alerting push services: http://www.lsis.com/channels/?query=93
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2012-02-05T11:10:59+01:00text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed02.02.2012 | NCBI PubMed: Does Terfenadine-Induced Ventricular Tachycardia/Fibrillation Directly Relate to Its QT Prolongation and Torsades de Pointes?
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Background:? We investigated the proarrhythmic potential of terfenadine in isolated rabbit hearts, left ventricular wedge preparations, and the effects on the human ether-a-go-go related gene (HERG) current in a human embryonic kidney cell line (HEK293) with a stable transfection of hERG and on I(Na) current not only in rabbit ventricular cells but also in human atrial myocytes. Methods and Results:? By means of the whole-cell patch-clamp recording, terfenadine concentration- and (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed02.02.2012 | NCBI PubMed: The CCK(2) receptor antagonist, JNJ-26070109, inhibits gastric acid secretion and prevents omeprazole-induced acid rebound in the rat.
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Background and purpose.? JNJ-26070109 is a novel CCK(2) receptor antagonist with good pharmacokinetic properties and represents a novel mechanism for the treatment of gastro-oesophageal reflux disease (GORD). The purpose of the present study was to determine whether chronic treatment with JNJ-26070109 could prevent as well as treat acid rebound in rats. Experimental approach.? A chronic fistula was surgically inserted into the stomach of rats to enable the measurement of acid secretion (…)text/htmlhttp://www.biospace.comBioSpace03.02.2012 | BioSpace: Johnson & Johnson (JNJ) Hid Risperdal Studies to Boost Drug Sales, Lawyer Says
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Johnson & Johnson hid studies showing its Risperdal anti-psychotic drug caused diabetes to protect billions of dollars in sales, a lawyer said in the first personal-injury claim over the medication to go to trial. Researchers at J&J s Janssen unit knew as early as 1999 that a study found Risperdal caused diabetes at a higher rate than a competing drug and failed to hand over the results to regulators probing links between the disease and anti-psychotic medicines, Fletch Trammell, a lawyer for (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed01.09.2009 | NCBI PubMed: 5-hydroxytryptamine receptor assays.
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5-Hydroxytryptamine (5-HT) receptors, by virtue of their broad expression pattern in peripheral and central tissues, regulate diverse physiological and behavioral responses through the activation of fourteen molecularly distinct receptor subtypes. The tissue-specific distribution of these receptors confers specificity for the actions of serotonin and highlights the therapeutic potential of serotonin receptor modulators. To better assess this therapeutic potential, it is useful to characterize (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed01.10.2006 | NCBI PubMed: In vivo animal models: quantitative models used for identifying antibacterial agents.
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Determining the in vivo bactericidal potential of novel agents is critical for selecting drug candidates. Described in this unit are two protocols that measure the amount of bacterial killing under very different conditions. The mouse pouch protocol is a rapid assay that provides efficacy data in an acute infection, whereas the rabbit tissue cage protocol assesses the ability of a compound to eradicate bacteria in a chronic abscess infection. Data from these tests, along with those from other (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed01.11.2011 | NCBI PubMed: Evolution of approaches to viral safety issues for biological products.
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CONFERENCE PROCEEDING Proceedings of the PDA/FDA Adventitious Viruses in Biologics: Detection and Mitigation Strategies Workshop in Bethesda, MD, USA; December 1-3, 2010 Guest Editors: Arifa Khan (Bethesda, MD), Patricia Hughes (Bethesda, MD) and Michael Wiebe (San Francisco, CA) Approaches to viral safety issues for biological products have evolved during the past 50+ years. The first cell culture products (viral vaccines) relied largely on the use of in vitro and in vivo virus screening (…)text/htmlhttp://www.biospace.comBioSpace02.02.2012 | BioSpace: National Institute for Clinical Excellence (NICE) Rejects Use of Johnson & Johnson (JNJ)'s Prostate Cancer Drug Zytiga
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A Johnson & Johnson prostate-cancer medicine discovered in England and developed with funds from U.K. charities is too expensive for the country s National Health Service. The NHS shouldn t pay for Zytiga because the drug s benefits don t justify the cost even after the manufacturer agreed to cut the price, the National Institute for Health and Clinical Excellence said in a statement today. The agency, known as NICE, advises the state-run medical system on which treatments it should pay for. (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed30.01.2012 | NCBI PubMed: Phospholipidosis in Rats Treated with Amiodarone: Serum Biochemistry and Whole Genome Micro-Array Analysis Supporting the Lipid Traffic Jam Hypothesis and the Subsequent Rise of the Biomarker BMP.
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To provide mechanistic insight in the induction of phospholipidosis and the appearance of the proposed biomarker di-docosahexaenoyl (C22:6)-bis(monoacylglycerol) phosphate (BMP), rats were treated with 150 mg/kg amiodarone for 12 consecutive days and analyzed at three different time points (day 4, 9, and 12). Biochemical analysis of the serum revealed a significant increase in cholesterol and phospholipids at the three time points. Bio-analysis on the serum and urine detected a time-dependent (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed31.01.2012 | NCBI PubMed: Role of Mixed Ion Channel Effects in the Cardiovascular Safety Assessment of the Novel Anti-MRSA Fluoroquinolone JNJ-Q2.
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Background and Purpose:? JNJ-Q2, a novel broad spectrum fluoroquinolone with anti-MRSA activity, was evaluated in a comprehensive set of nonclinical and clinical cardiovascular safety studies. The effect of JNJ-Q2 on different cardiovascular parameters was compared to that of moxifloxacin, sparfloxacin and ofloxacin. Through comparisons to these well-known fluoroquinolones, the importance that compensatory ion channel effects have on the cardiovascular safety of JNJ-Q2 was investigated. (…)text/htmlhttp://www.biospace.comBioSpace01.02.2012 | BioSpace: Manifesto Release: Johnson & Johnson (JNJ) and Medtronic, Inc. (MDT) Reducing Asia Pacific Operations
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February 01, 2012 - Global medical device players, Johnson & Johnson and Medtronic, are re-organising their Asia Pacific operations and transitioning back to more global business models. This effectively reduces the strategic management layer at the Asia Pacific level. Some say this could be to a) improve communications directly globally and/or b) reduce costs as having additional regional structures cuts into profits. Both Johnson & Johnson and Medtronic have been moving significant (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed28.01.2012 | NCBI PubMed: Control of cilostazol release kinetics and direction from a stent using a reservoir-based design.
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Sustained release formulations of a potent antithrombotic drug, cilostazol, in poly-(lactic acid-co-glycolic acid) (PLGA) matrices were created for luminal release from a novel drug-eluting stent utilizing reservoirs (RES TECHNOLOGY?). The crystallinity of cilostazol and the morphology of the cilostazol/polymer matrix in the stent reservoirs were examined by cross-polarized optical microscopy and differential scanning calorimetry. An in vitro method was developed to study release kinetics of (…)text/htmlhttp://www.biospace.comBioSpace31.01.2012 | BioSpace: Johnson & Johnson (JNJ) Shakes Up McNeil Consumer Healthcare Unit Again
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Johnson & Johnson is shaking up oversight of the troubled unit that makes Tylenol and other over-the-counter medicines once again, naming new leadership less than a year after manufacturing problems sparked a revamp. The New Brunswick, N.J., health-products giant is replacing two company group chairmen who held key roles trying to turn around a consumer business racked by recalls and more than $1 billion in lost sales of popular cold, pain and allergy medicines. Patrick Mutchler, who was put (…)text/htmlhttp://www.biospace.comBioSpace31.01.2012 | BioSpace: International Mental Health Research Organization Announces 2012 IMHRO Rising Star Awards for Mental Health Research
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RUTHERFORD, Calif.-(BUSINESS WIRE)-The International Mental Health Research Organization (IMHRO) has announced its 2012 IMHRO Rising Star Translational Research Awards, which are sponsored by IMHRO and Johnson & Johnson Services, Inc. IMHRO and the Corporate Office of Science and Technology of Johnson & Johnson Services, Inc. identify and fund critical and cutting edge research on the causes of and cures for brain disorders. IMHRO serves as an umbrella organization to provide support for (…)text/htmlhttp://www.biospace.comBioSpace31.01.2012 | BioSpace: Health Warning Over DePuy Orthopaedics, Inc. (JNJ)'s Hip Implants
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New York, New York (PRWEB) January 30, 2012 - Bernstein Liebhard LLP reports that health regulators in Britain are concerned that recipients of the metal-on-metal DePuy ASR hip implants were never notified that the devices were recalled.* In August 2010, DePuy Orthopaedics, a subsidiary of Johnson & Johnson, issued a voluntary worldwide recall of its ASR hip implant systems, after receiving data from the National Joint Registry of England and Wales that 1 out of every 8 patients (12%-13%) who (…)text/htmlhttp://www.uspto.gov/USPTO30.07.2004 | USPTO: Compositions and methods for treating skin conditions
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United States Patent: 8106094 |-| Title: Compositions and methods for treating skin conditions |-| Inventors: Sah; Archana (Redmond, WA), Dole; Victoria (Whitehouse Station, NJ), Nystrand; Glenn (Lebanon, NJ), Seiberg; Miri (Princeton, NJ), Liu; Jue-Chen (Belle Mead, NJ), Kurtz; Ellen (Ringoes, NJ) |-| Assignee: Johnson & Johnson Consumer Companies, Inc. (Skillman, NJ) |-| This invention relates to methods and compositions for treating and ameliorating skin conditions including post (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed23.01.2012 | NCBI PubMed: Oxidative degradation studies of an oxazolidinone-derived antibacterial agent, RWJ416457, in aqueous solutions.
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The rates of oxidative degradation of a new antibacterial drug, RWJ416457, in aqueous solutions were investigated over the pH-range of 2 to 10. Two oxidative degradates were identified and the influences of pH, buffer concentration, metal ions, metal chelating agents, and temperatures were studied. The pH, metal chelating agents, and metal ions significantly changed the product distribution in addition to the degradation rate. Oxidative degradation is believed to follow a hydrogen abstraction (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed20.01.2012 | NCBI PubMed: Standardized Diaper Care Regimen: A Prospective, Randomized Pilot Study on Skin Barrier Function and Epidermal IL-1? in Newborns.
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? Adaptation of skin barrier function and interleukin-1? (IL-1?) content in diapered and nondiapered skin are poorly characterized in newborns receiving standard skin care. In a monocentric, prospective pilot study 44 healthy, full-term neonates were randomly assigned to skin care with baby wipes (n?=?21) or water-moistened washcloth (n?=?23) at each diaper change. Transepidermal water loss (TEWL), skin hydration, skin-pH, IL-1?, and epidermal desquamation were measured on days 2, (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed17.01.2012 | NCBI PubMed: Pharmacological dissection of K(v) 7.1 channels in systemic and pulmonary arteries.
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Background and purpose.? The aim of this study was to characterize the functional impact of KCNQ1-encoded voltage-dependent potassium channels (K(v) 7.1) in the vasculature. Experimental approach.? Mesenteric arteries, intrapulmonary arteries and thoracic aortae were isolated from adult rats. K(v) 7.1 channel expression was established by fluorescence immunocytochemistry. Wire myography determined functionality of these channels in response to selective blockers and activators. Xenopus (…)text/htmlhttp://www.biospace.comBioSpace25.01.2012 | BioSpace: National Institute for Clinical Excellence (NICE) Backs Bristol-Myers Squibb Company (BMY), Pfizer Inc. (PFE)'s Eliquis
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Pfizer Inc. and Bristol-Myers Squibb Co. s blood-thinner apixaban won a final recommendation from the U.K. s health-cost agency. The pill, also known by the brand name Eliquis, may be used to prevent blood clots in adults who have undergone hip or knee replacement surgery, the National Institute for Health and Clinical Excellence said in a statement today. The agency, known as NICE, advises the state-run National Health Service on which treatments represent value for money. Almost 120,000 hip (…)text/htmlhttp://www.biospace.comBioSpace25.01.2012 | BioSpace: Johnson & Johnson (JNJ) Won't Reopen Shuttered Plant Until 2013
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The McNeil Consumer Healthcare plant in Fort Washington, Montgomery County, will not resume production until at least 2013, Johnson & Johnson's chief executive officer, Bill Weldon, said Tuesday as the company reported 2011 full-year and fourth-quarter financial results. Recalls, repairs, litigation, and costs related to the acquisition of Synthes Inc. played a big part in J&J's profit dropping 88.8 percent in the fourth quarter of 2011 compared with the same period a year earlier. Companies (…)text/htmlhttp://www.biospace.comBioSpace20.01.2012 | BioSpace: Tennessee Hip Replacement Patient Files Suit Against DePuy Orthopaedics, Inc. (JNJ) For Alleged Debilitating Injuries
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NASHVILLE, Tenn.-(BUSINESS WIRE)-Kathryn E. Barnett of the national plaintiffs law firm Lieff Cabraser Heimann & Bernstein, LLP, announced that Paul McCurley of Chattanooga, Tennessee, has filed a lawsuit against DePuy Orthopaedics, Inc., and its parent company, Johnson & Johnson, Inc., for the injuries he suffered after his DePuy Pinnacle metal on metal hip implant failed. The lawsuit charges that DePuy knew that the Pinnacle metal on metal hip generated unusual and dangerous levels of (…)text/htmlhttp://www.biospace.comBioSpace20.01.2012 | BioSpace: Covidien plc (COV) CEO Almeida to Add Chairman Title
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DUBLIN-(BUSINESS WIRE)- Covidien plc (NYSE: COV - News) today announced that its Board of Directors has elected President and Chief Executive Officer José E. Almeida to the additional position of Chairman of the Board, effective March 13, 2012. Mr. Almeida will succeed Richard J. Meelia, who has served as Chairman since October 2008. Mr. Meelia agreed to serve as Non-Executive Chairman of the Board for a transition period of up to one year following his July 2011 retirement as President (…)text/htmlhttp://www.biospace.comBioSpace20.01.2012 | BioSpace: Johnson & Johnson (JNJ) to Pay $158 Million to Settle Texas Risperdal Case
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Johnson & Johnson said on Thursday it will pay $158 million to settle a Texas lawsuit accusing the drugmaker of improperly marketing its Risperdal anti-psychotic drug to state residents on the Medicaid health program for the poor. The settlement fully resolves all Risperdal-related claims in Texas, the company said. The agreement is specific to the state of Texas and does not involve other ongoing state or federal Risperdal litigation. The deal settles claims brought by Texas in 2004 and (…)text/htmlhttp://www.biospace.comBioSpace20.01.2012 | BioSpace: La Jolla Pharmaceutical Company (LJPC) Acquires GCS-100, a First-in-Class Galectin-3 Antagonist; CEO Appointed
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SAN DIEGO-(BUSINESS WIRE)- La Jolla Pharmaceutical Company (OTCBB: LJPC.PK - News) (the Company and La Jolla ) today announced that it has acquired global development and commercialization rights to GCS-100, a novel therapeutic, from privately held Solana Therapeutics, Inc. ( Solana ). GCS-100 is a first-in-class inhibitor of galectin-3, a novel molecular target implicated in cancer and chronic organ failure. In connection with the acquisition, George F. Tidmarsh, M.D., Ph.D., (…)text/htmlhttp://www.biospace.comBioSpace19.01.2012 | BioSpace: Espicom Release: Rapid Rise in Opioid Abuse is Among the Challenges Faced by Pain Therapy Drug Developers
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Chichester, UK (PRWEB) January 9, 2012 According to a new Espicom report, Evolution in the Pain Therapy Market: Nociceptive and Neuropathic Drug Development, despite a plethora of medications, the pain market remains an area of high unmet need as current therapies are often less than effective and/or have undesirable side effects. Among the challenges facing the pharmaceutical industry is the rapid rise in prescription drug abuse, particularly in the US, where it has reached epidemic (…)text/htmlhttp://www.biospace.comBioSpace19.01.2012 | BioSpace: Welsh Government Teams Up With Oxford Innovation to Boost Growth of Life Sciences Firms in Wales
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19 January 2012 - Oxford Innovation has been appointed by the Welsh Government to deliver a new programme that will assist start-up and early stage life sciences firms with high growth potential to grow more rapidly over the next three years. The High Potential Starts programme is a key component of the Welsh Government s strategy to support sustainable high growth businesses. The programme is jointly funded by the Welsh Government and the European Regional Development Fund. The programme (…)text/htmlhttp://www.biospace.comBioSpace19.01.2012 | BioSpace: Johnson & Johnson (JNJ) Hid 3 Risperdal Diabetes Studies from FDA: Witness
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Johnson & Johnson officials hid three studies showing some patients using Risperdal developed diabetes while claiming the antipsychotic drug didn t cause the disease, a witness testified. As early as 1999, Johnson & Johnson s Janssen unit had researchers findings that about half the patients taking Risperdal in a study comparing its risks to those of Eli Lilly & Co. s Zyprexa antipsychotic drug developed diabetes after a year on the medication, Joseph Glenmullen, a psychiatrist and Harvard (…)text/htmlhttp://www.biospace.comBioSpace19.01.2012 | BioSpace: FDA Warns Johnson & Johnson (JNJ)'s DePuy Orthopaedics, Inc. (JNJ) Unit on Custom Devices
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Johnson & Johnson subsidiary Depuy Orthopaedics decides to stop selling all custom devices following an FDA letter warning the company to file new PMA and 510(k) applications for several components. Johnson & Johnson (NYSE:JNJ) subsidiary DePuy Orthopaedics decided to stop selling all custom fitted devices in response to an FDA warning following an inspection of the Warsaw, Ind.-based company's facilities. This week the FDA's Centers for Devices & Radiological Health released a letter warning (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed16.01.2012 | NCBI PubMed: Disinfection of Flexible Fiberoptic Laryngoscopes After In Vitro Contamination With Staphylococcus aureus and Candida albicans.
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OBJECTIVE: To determine the efficacy of various cleaning and disinfective methods in reducing bacterial and fungal load on flexible fiberoptic laryngoscopes (FFLs). DESIGN: In vitro model. SUBJECTS: Flexible fiberoptic laryngoscopes contaminated with Staphylococcus aureus and Candida albicans. INTERVENTIONS: Contamination with S aureus and C albicans was separately induced on FFLs, which were then disinfected with different protocols: 20-, 15-, 10-, and 5-minute soaks in (…)text/htmlhttp://www.biospace.comBioSpace18.01.2012 | BioSpace: Johnson & Johnson (JNJ) Opens San Diego Biotech Startup Center, Says "No Strings Attached"
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Johnson & Johnson s West Coast research leader, Diego Miralles, has met with a lot of biotech entrepreneurs who are curious about what J&J is doing to foster more startups at its facility in San Diego. At some point, a skeptical question usually comes up. What s the catch? Miralles says he s sometimes asked. He insists there isn t any catch. We are genuinely trying to help the industry, Miralles said last week in a meeting at the JP Morgan Healthcare Conference in San Francisco. We (…)text/htmlhttp://www.biospace.comBioSpace18.01.2012 | BioSpace: FDA Misses Deadline in Clash With Device-Makers Over Reviews
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U.S. regulators haggling with medical-device makers over how much it will cost to speed up product reviews starting this year missed a legal deadline to submit a proposal for congressional approval. Under a 2007 law, the companies, led by Johnson & Johnson and Medtronic Inc., were charged $295 million over five years to get products such as hip implants and heart stents reviewed in a timely manner. The law, set to be reauthorized this year, mandates that the agency submit a new agreement to (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed01.02.2012 | NCBI PubMed: Comparisons between in vitro whole cell imaging and in vivo zebrafish-based approaches for identifying potential human hepatotoxicants earlier in pharmaceutical development.
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Drug-induced liver injury (DILI) is a major cause of attrition during both the early and later stages of the drug development and marketing process. Reducing or eliminating drug-induced severe liver injury, especially those that lead to liver transplants or death, would be tremendously beneficial for patients. Therefore, developing new pharmaceuticals that have the highest margins and attributes of hepatic safety would be a great accomplishment. Given the current low productivity of (…)text/htmlhttp://www.biospace.comBioSpace17.01.2012 | BioSpace: Johnson & Johnson (JNJ) Marketed Rispersal for Children After FDA Warnings, Texas Jury Told
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The antipsychotic drug Risperdal was marketed for children and adolescents by Johnson & Johnson s Janssen unit after warnings by the U.S. Food and Drug Administration not to do so, a witness told jurors. Janssen s marketing to children began after the drug s introduction in 1994 and continued until the FDA s first approval for pediatric uses in 2006, jurors in state court in Austin, Texas, heard yesterday from attorney Arnold Friede, an expert witness for the state. Texas seeks at least $579 (…)text/htmlhttp://www.biospace.comBioSpace17.01.2012 | BioSpace: Social Media On the Job: What Goes Wrong When the Boss Spooks Employees as an Online Space Invader
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Second City Communications and Corpedia Release Funny and Engaging Video Called Company Retreating Exploring Boundaries and Privacy When Using Social Media At The Office Company Retreating is One of Many Timely, Relevant Videos on Ethics and Compliance Topics Served Up In the Innovative Video Library Called RealBiz Shorts CHICAGO-(BUSINESS WIRE)- Just because the boss can connect with employees through online social networks, is it a good idea? And if managers do connect to (…)text/htmlhttp://www.uspto.gov/USPTO21.05.2008 | USPTO: Multitargeting interfering RNAs having two active strands and methods for their design and use
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United States Patent: 8097715 |-| Title: Multitargeting interfering RNAs having two active strands and methods for their design and use |-| Inventors: Rivory; Laurent Pierre (New South Wales, AU), Poidinger; Michael (New South Wales, AU), Birkett; Donald John (New South Wales, AU), Arndt; Gregory Martin (New South Wales, AU), Passioura; Toby (New South Wales, AU) |-| Assignee: Johnson & Johnson Research PTY Limited (Eveleigh, NSW, AU) |-| Interfering RNA molecules are now designed and produced (…)text/htmlhttp://www.biospace.comBioSpace12.01.2012 | BioSpace: Biosense Webster, Inc. (JNJ) Announces FDA Approval of the THERMOCOOL SF Catheter in the United States
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DIAMOND BAR, Calif.-(BUSINESS WIRE)- Biosense Webster, Inc., a worldwide leader in the diagnosis and treatment of cardiac arrhythmias, announced the FDA approval of the new THERMOCOOL SF irrigated ablation catheter in the United States. The THERMOCOOL SF NAV Catheter combines Biosense Webster s latest irrigated ablation technology with the accurate visualization of the CARTO3 3D Mapping & Ablation System. The catheter was launched in Europe in October, 2010 and has received excellent (…)text/htmlhttp://www.biospace.comBioSpace12.01.2012 | BioSpace: Johnson & Johnson (JNJ)'s Subsidiary, Cilag AG International (JNJ), to Shed 120 Jobs in Schaffhausen
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Drug maker Cilag in the canton of Schaffhausen says it will shed 120 jobs. Cilag has about 1,100 employees but it says it plans to drop a large part of its active ingredient production by 2015. The pharmaceutical company said increasing price pressure has driven it to look at products with higher margins and growth potential. Cilag is a subsidiary of U.S. giant Johnson & Johnson and is a major employer in Schaffhausen. The company said it hoped most of the job cuts would come through natural (…)text/htmlhttp://www.biospace.comBioSpace11.01.2012 | BioSpace: Johnson & Johnson (JNJ) Sold Insulin Pumps After Learning of Defects, FDA Says
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Johnson & Johnson s Animas unit kept selling insulin pumps last year after learning of malfunctions with the devices that prompted it to make design changes, the Food and Drug Administration said. The agency faulted the J&J unit for not adequately explaining why your firm continued to manufacture insulin pumps after they had known failures. The issues with Animas One Touch Ping and 2020 pumps prompted a company investigation that started in April, according to the FDA s letter, which (…)text/htmlhttp://www.biospace.comBioSpace11.01.2012 | BioSpace: Johnson & Johnson (JNJ) to Shut Down R&D Facility, 126 Jobs Cut
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On the heels of Quebec's worst three-month jobs losses in a generation, Johnson & Johnson says it is closing its research centre in the province. New Jersey-based J&J, the world's biggest health care products company, told employees at its Montreal research and development centre Tuesday morning that the facility would shut down in March. Some 126 people work at the centre, including 36 J&J employees and 90 from a private placement agency hired on a contract basis, said the company's Quebec (…)text/htmlhttp://www.biospace.comBioSpace11.01.2012 | BioSpace: Medtronic, Inc. (MDT) Loses International President to Competitor
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Minneapolis / St. Paul Business Journal by Ed Stych, Web Producer Medtronic Inc. has lost the president of its international operations, as Jean-Luc Butel has taken a similar position with competitor Baxter International Inc. Butel, 55, will report to Baxter CEO Robert Parkinson Jr. and will start his new job as president of international operations on Feb. 20, according to a Baxter news release. Parkinson said in a statement that Butel's international experience will help Deerfield, (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed06.01.2012 | NCBI PubMed: Canagliflozin Improves Glycemic Control Over 28 Days in Subjects With Type 2 Diabetes Not Optimally Controlled on Insulin.
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Aims: Canagliflozin is a sodium-glucose co-transporter 2 (SGLT2) inhibitor that is being investigated for the treatment of type 2 diabetes mellitus (T2DM). Methods: This was a randomized, double-blind, placebo-controlled, parallel-group, 28-day study conducted at 2 sites, in 29 subjects with T2DM not optimally controlled on insulin and up to 1 oral antihyperglycemic agent. Subjects were treated with canagliflozin 100 mg QD or 300 mg BID or placebo. Safety, tolerability, pharmacokinetic (…)text/htmlhttp://www.biospace.comBioSpace10.01.2012 | BioSpace: Norwich Pharmaceuticals Expands Product Development Services
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January 10, 2012 - Norwich, a leader in full-service contract development and manufacturing, is expanding its services to now include small scale feasibility and initial product development for prescription and over-the-counter pharmaceuticals. The non-GMP development facility will offer Norwich customers greater flexibility and speed when assessing the feasibility of technical concepts and formulations, and create streamlined progression from clinical into scale-up and through commercial (…)text/htmlhttp://www.biospace.comBioSpace10.01.2012 | BioSpace: Plasticell to Collaborate With Pfizer Inc. (PFE) and University of Sheffield in a Cellzome-led £1.4 Million Technology Strategy Board-funded Stem Cell Project
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London, 10 January 2012 - Plasticell, the biotechnology company specialising in high throughput technologies for directed stem cell differentiation, has announced that the Technology Strategy Board has funded a research consortium comprising of Plasticell, Pfizer (Neusentis) and the University of Sheffield, led by Cellzome. The project will develop methods of characterizing stem cells through protein fingerprints predictive of changes in stem cell behaviour. The Technology Strategy Board will (…)text/htmlhttp://www.biospace.comBioSpace10.01.2012 | BioSpace: Norwich Pharmaceuticals Introduces Clinical Services Division
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January 10, 2012 - Norwich, a leader in full-service contract development and manufacturing, is expanding its services to now include small scale feasibility and initial product development for prescription and over-the-counter pharmaceuticals. The non-GMP development facility will offer Norwich customers greater flexibility and speed when assessing the feasibility of technical concepts and formulations, and create streamlined progression from clinical into scale-up and through commercial (…)text/htmlhttp://www.biospace.comBioSpace10.01.2012 | BioSpace: Boehringer Ingelheim Corporation's Pradaxa Increases Risk of Heart Attack, Study Shows
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Boehringer Ingelheim GmbH s anti- coagulant Pradaxa increases a patient s risk of heart attack or severe chest pain, according to a review of studies conducted on the drug. An analysis of seven clinical trials found that it was significantly associated with a higher risk of heart attacks and acute coronary syndrome, or ACS, a designation that includes heart attacks and chest pain, researchers wrote in a report published today in the Archives of Internal Medicine. The potential risk of (…)text/htmlhttp://www.uspto.gov/USPTO10.09.2003 | USPTO: Methods for treating skin conditions
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United States Patent: 8093293 |-| Title: Methods for treating skin conditions |-| Inventors: Seiberg; Miri (Princeton, NJ), Liu; Jue-Chen (Belle Mead, NJ), Iotsova; Violetta (Robbinsville, NJ) |-| Assignee: Johnson & Johnson Consumer Companies, Inc. (Skillman, NJ) |-| This invention relates to methods and compositions for treating and ameliorating skin conditions including acne, rosacea and wrinkling caused by photodamage or intrinsic aging. More particularly, this invention relates to (…)text/htmlhttp://www.uspto.gov/USPTO05.08.2008 | USPTO: Absorbent article including absorbent core having a plurality of first regions and a second region surrounding each of the first regions
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United States Patent: 8093448 |-| Title: Absorbent article including absorbent core having a plurality of first regions and a second region surrounding each of the first regions |-| Inventors: De Carvalho; Antonio Carlos Ribeiro (Taubate, BR), Fajolli; Marcia Helena Teixeira (Sao Jose dos Campos, BR), Salles; Maria Marcia R. Caldas (Sao Jose dos Campos, BR) |-| Assignee: Johnson & Johnson Ind. E. Com LTDA (BR) |-| An absorbent article including a absorbent core having a plurality of first (…)text/htmlhttp://www.biospace.comBioSpace09.01.2012 | BioSpace: KMR Group Release: Pharmaceutical Benchmarking Forum's Success Rate Data Illuminates Challenges to R&D Industry
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CHICAGO, Illinois, January 9, 2012 - Only 10% of molecules that enter Phase II will reach market, according to recent analysis by the Pharmaceutical Benchmarking Forum (PBF). And that is on top of growing attrition rates in earlier phases for preclinical and initial human studies that make the overall challenge of bringing drugs through Development even greater. This analysis is based on very detailed data from the PBF - which consists of the leading pharmaceutical companies - and offers the (…)text/htmlhttp://www.ncbi.nlm.nih.govNCBI PubMed01.02.2012 | NCBI PubMed: Real-time ultrasound imaging of irreversible electroporation in a porcine liver model adequately characterizes the zone of cellular necrosis.
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Background:? Irreversible electroporation (IRE) is a largely non-thermal method for the ablation of solid tumours. The ability of ultrasound (US) to measure the size of the IRE ablation zone was studied in a porcine liver model. Methods:? Three normal pig livers were treated in vivo with a total of 22 ablations using IRE. Ultrasound was used within minutes after ablation and just prior to liver harvest at either 6?h or 24?h after the procedure. The area of cellular necrosis was (…)text/htmlhttp://www.biospace.comBioSpace06.01.2012 | BioSpace: Johnson & Johnson (JNJ) to Pay $1 Billion to Settle Risperdal Marketing Probe
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Johnson & Johnson will pay more than $1 billion in civil and criminal penalties to the federal government and individual states to settle an investigation into the marketing practices of its anti-psychotic drug Risperdal, Bloomberg News Service reported Thursday. The figure would be in line with what Eli Lilly & Co. paid three years ago to settle claims that it marketed a similar anti-psychotic drug, Zyprexa, for illnesses that weren t approved by the U.S. Food and Drug Administration. These (…)