Application for Regulatory Approvals, Conferences and Presentations, and Enrollment in Clinical Trials - Research Report on Gilead, Alnylam, Omeros, PTC, and Stemline PR Newswire NEW YORK, September 26, 2013 NEW YORK, September 26, 2013 /PRNewswire/ -- Editor Note: For more information about this release, please scroll to bottom. Today, Investors' Reports announced new research reports highlighting Gilead Sciences Inc. (NASDAQ: GILD), Alnylam Pharmaceuticals, Inc. (NASDAQ: ALNY), Omeros Corporation (NASDAQ: OMER), PTC Therapeutics, Inc. (NASDAQ: PTCT), and Stemline Therapeutics, Inc. (NASDAQ: STML). Today's readers may access these reports free of charge - including full price targets, industry analysis and analyst ratings - via the links below. Gilead Sciences Inc. Research Report On September 11, 2013, Gilead Sciences Inc. (Gilead) announced its submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for approval of idelalisib for the treatment of indolent non-Hodgkin's lymphoma (iNHL). According to Gilead, the data submitted for the NDA support the use of idelalisib for patients with iNHL that is refractory (non-responsive) to rituximab and to alkylating-agent-containing chemotherapy. John C. Martin, PhD, Chairman and CEO of Gilead Sciences, stated, "Based on the rate and duration of response observed to date in this highly refractory iNHL patient population, we believe idelalisib could become an important new therapy for patients who have limited treatment options." According to Gilead, Idelalisib is an investigational, targeted, highly selective oral inhibitor of phosphoinositide 3-kinase (PI3K) delta: a protein that is critical for the activation, proliferation and survival of B lymphocytes. The Full Research Report on Gilead Sciences Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.InvestorsReports.com/report/2013-09-23/GILD] -- Alnylam Pharmaceuticals, Inc. Research Report On September 20, 2013, Alnylam Pharmaceuticals, Inc. (Alnylam) announced that its management will give an overview of the Company during the upcoming 20th Annual NewsMakers in the Biotech Industry Conference. Alnylam reported that the presentation will be held at 2:30 p.m. ET, on September 27, 2013 at the Millennium Broadway Hotel in New York City. The Company also stated that a live audio webcast will be available on the News & Investors section of its website. Further, the archive of the presentation will also be available on its website within 48 hours after the conclusion of the event. The Full Research Report on Alnylam Pharmaceuticals, Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.InvestorsReports.com/report/2013-09-23/ALNY] -- Omeros Corporation Research Report On September 19, 2013, Omeros Corporation (Omeros) announced the initiation of enrollment in a Phase 2 clinical trial of OMS824, the Company's phosphodiesterase 10 (PDE10) inhibitor. Gilead reported that the trial will evaluate the compound's tolerability, safety, pharmacokinetics, potential interactions with concomitant antipsychotic medications, and a battery of cognitive tests in patients with stable schizophrenia. According to Omeros, PDE10 is an enzyme that is expressed in areas of the brain linked to diseases that affect cognition and psychomotor functions, including Huntington's disease and schizophrenia. The Company stated that in this Phase 2 clinical trial, OMS824 will be administered at various dose levels for two weeks to patients whose antipsychotic medications have been temporarily discontinued or who continue their usual antipsychotic regimen in order to assess the effects of OMS824 as monotherapy and in combination with antipsychotic medications. Gregory A. Demopulos, M.D., Chairman and CEO of Omeros, said, "This Phase 2 trial will provide us with important information on our compound's safety and, potentially, efficacy for additional Phase 2 trials in schizophrenia and Huntington's disease. We look forward to completing the current trial later this year." The Full Research Report on Omeros Corporation - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.InvestorsReports.com/report/2013-09-23/OMER PTC Therapeutics, Inc. Research Report On September 18, 2013, PTC Therapeutics, Inc. (PTC) announced that two of its abstracts have been accepted for the 10th European Pediatric Neurology Society Congress (EPNS) in Brussels, Belgium, to be held from September 25, 2013 to September 28, 2013. According to the Company, the two abstracts are: Design of a confirmatory phase 3, multicenter, randomized, double-blind, placebo-controlled study of ataluren in patients with nonsense mutation Duchenne muscular dystrophy; and Disease-related symptoms and activities of daily living: a novel survey of patients with nonsense mutation Duchenne muscular dystrophy, which will be presented on September 25, 2013 at 13:30 p.m. PTC also informed that it will sponsor a symposium at EPNS titled New perspectives in the management of Duchenne muscular dystrophy on September 25, 2013 from 12:30 p.m. to 13:30 p.m. The Full Research Report on PTC Therapeutics, Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.InvestorsReports.com/report/2013-09-23/PTCT] -- StemlineTherapeutics, Inc. Research Report On September 19, 2013, Stemline Therapeutics, Inc. (Stemline) announced that the Company will be participating at the Aegis Capital Corporation 2013 Healthcare Conference to be held at the Encore at Wynn Las Vegas from September 26, 2013 to September 28, 2013. Stemline informed that Ivan Bergstein, M.D., CEO of the Company, will give a presentation at the event on September 28, 2013 at 9:45 a.m. PDT. The Full Research Report on Stemline Therapeutics, Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.InvestorsReports.com/report/2013-09-23/STML] ---- EDITOR NOTES: 1.This is not company news. We are an independent source and our views do not reflect the companies mentioned. 2.Information in this release is fact checked and produced on a best efforts basis and reviewed by Namrata Maheshwari, a CFA charterholder. However, we are only human and are prone to make mistakes. 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Application for Regulatory Approvals, Conferences and Presentations, and Enrollment in Clinical Trials - Research Report on
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