Sage Therapeutics and Biogen announce positive pivotal phase 3 results for zuranolone, an investigational two-week, once-daily therapeutic being evaluated for major depressive disorder. Sage Therapeutics to host conference call today at 8 a.m. On average, they expect Sage Therapeutics' share price to reach $82.19 in the next year. Subscribe to Yahoo Finance Plus to view Fair Value for SAGE. We have recently updated our Privacy Policy to include information regarding the cookies we collect. Sage Therapeutics Inc . Sage Therapeutics announces FDA approval of Zulresso (brexanolone) injection, the first and only treatment specifically indicated for postpartum depression [news release]. Sage is exploring new disease pathways for certain neurologic disorders. Tucked in the Q2 earnings release, Sage Therapeutics Inc (NASDAQ: SAGE) has terminated two long-suspended Phase 3 zuranolone trials in major depressive disorder (MDD). Tuesday 8/10 Insider Buying Report: SAGE, UNVR. Connect with our staff on topics that matter to you via email or request a reprint. Zuranolone, a potential first-in-class, two-week, once-daily oral therapy in development for the treatment of MDD and PPD, is currently in Phase 3 development as part of the LANDSCAPE and NEST clinical programs. Together, these two features, if supported by positive clinical efficacy and safety data, could provide an alternative option to how depression is treated today based on a target profile of an “as-needed” short course of treatment for a depressive episode, with rapid and sustained efficacy and favorable tolerability. TherapeuticsMD Announces Issuance of a J-Code for ANNOVERA® to Be Utilized in the Public Health Sector. A high-level overview of Sage Therapeutics, Inc. (SAGE) stock. Rather, the main focus of Sage's first quarter earnings report was an experimental drug that may provide a major lift to the company's business later on. May 26, 2021. Found insideC. Neill Epperson 1) Consulting to Sage Therapeutics, Shire and Asarina Pharma 2) Grant funding: Sage Therapeutics 3) Minor stock holder for personal investments: BMS and Merck 4) Minor stock holder: Husband's investments: Abbott, J&J, ... SAGE THERAPEUTICS, INC. : Press releases relating to SAGE THERAPEUTICS, INC. Investor relations | Börse Stuttgart: SG7 | Börse Stuttgart EQUITY ALERT: Rosen Law Firm Announces Investigation of Securities Claims Against Sage Therapeutics, Inc. - SAGE. Get prepared with the key expectations. Maureen L. SudaSage TherapeuticsTel: (617) 949-4289 Download. Investors should consider this cautionary statement as well as the risks factors identified in Biogen’s most recent annual or quarterly report and in other reports Biogen has filed with the U.S. Securities and Exchange Commission. Jeff Jonas, M.D., CEO of SAGE, says this in the Sage Therapeutics news release. SAGE MEDIA CONTACT: Maureen L. Suda Sage Therapeutics Tel: (617) 949-4289 Email: Maureen.Suda@sagerx.com BIOGEN MEDIA CONTACT: Allison Parks +1 781-464-3260 public.affairs@biogen.com SAGE INVESTOR . This news release contains forward-looking statements, made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, including statements relating to: the potential benefits and results that may be achieved through Sage’s proposed collaboration with Biogen; the anticipated completion of the proposed transaction; the anticipated payments that may be received if all milestones under the agreement with Biogen are met; the potential benefits, safety and efficacy of zuranolone and SAGE-324, and the potential of the product candidates, if successful, to change the way certain diseases and disorders are treated; the planned clinical development program and expected timing of data readouts for zuranolone and SAGE-324; the potential for successful development and approval of zuranolone and SAGE-324 and the potential for future commercialization; estimates as to the number of patients with MDD, PPD and essential tremor; and the goals, opportunity and potential for Sage’s business. Brexanolone IV submission is the Company's first New Drug Application. The study (n=67 full . PDF Version. Closing of the transaction is contingent on completion of review under antitrust laws, including the Hart-Scott-Rodino (HSR) Antitrust Improvements Act of 1976 in the U.S., and other customary closing conditions. Press release content from Business Wire. Half Year 2020 Results investor factsheet. Found inside – Page 1000A tripartite model of the therapeutic relationship: Theory, research, and practice. Psychotherapy Research, 24(2), 117–132. ... New York, NY: Oxford University Press. ... Thousand Oaks, CA: Sage. Gallegos, R. A., Criado, J. R., Lee, ... Their current portfolio targets multiple forms of depression, as well as cognitive dysfunction related to . Found inside – Page 278But the drugmaker set the price at $34,000, instantly putting it out of reach for most women — especially since health insurance companies may not cover the treatment.8 On an earnings call last year, Sage Therapeutics CEO Jeff Jonas ... Press Release reported 18 hours ago that Sage Therapeutics Announces Second Quarter 2021 Financial Results and Highlights Pipeline and Business Progress Found inside – Page 474Media culture: Cultural studies, identity and politics between the modern and the postmodern. London: Routledge. ... From salvation to selfrealization: Advertising and the therapeutic roots of the consumer culture, 1880–1930. Sage Therapeutics to Provide Update on Key 2019 Initiatives at J.P. Morgan Healthcare Conference - Multi-franchise strategy ongoing in depression, neurology and neuropsychiatry - On track for full commercial launch in the U.S. in late June. This suggests a possible upside of 74.5% from the stock's current price. Biogen discovers, develops and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases as well as related therapeutic adjacencies. Found insideRieff, P. (1966) The Triumph of the Therapeutic: uses of faith after Freud, London: Chatto and Windus. ... Royal Society (2004) 'Scientific Value of Human Remains Must be Given Proper Recognition', press release, London: The Royal ... Stay up to date on the latest stock price, chart, news, analysis, fundamentals, trading and investment tools. However, Sage-217 only achieved a mean score of 12.6. If you purchased shares of Sage Therapeutics on or before March 22, 2016 and would like to join the action, please click "Join This Class Action" above. Press Release. Sage Therapeutics to Present at Bank of America Merrill Lynch 2019 Health Care Conference. --(BUSINESS WIRE)--Oct. 9, 2019-- Sage Therapeutics (NASDAQ:SAGE), a biopharmaceutical company committed to developing novel therapies with the potential to transform the lives of people with debilitating disorders of the brain, today announced it will host a live webcast on. “Major depressive disorder affects approximately 17 million people in the U.S. alone, and is a common co-morbidity of multiple neurological disorders in Biogen’s core therapeutic areas. Found inside – Page 1Exelixis Press Release 22 JUNOO BioWorld Today 23JUNOO Vol ( No ) 11 ( 122 ) page ( s ) 2 conditions to permit net ... Molecular Oncology 188143 MEMOREC has licensed SAGE ( TM ) ( serial analysis of gene expression ) technology from ... Sage Therapeutics Safe Harbor This news release contains forward-looking statements, made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, including statements relating to: the potential benefits and results that may be achieved through Sage's proposed collaboration with Biogen; the anticipated . This press release features multimedia. Found inside – Page 38Washington, DC: Georgetown University Press. pp. 1–44. ... Labov, W. and Fanshel, D. (1977) Therapeutic Discourse: Psychotherapy as Conversation. ... Sociolinguistics: Proceedings of the UCLA Sociolinguistics Conference, 1964. Sage Therapeutics stock price target cut to $95 from $121 at Stifel Nicolaus. Sage Therapeutics Inc. (NASDAQ:SAGE) went down by -3.71% from its latest closing price compared to the recent 1-year high of $98.39. 14, 2019-- Sage Therapeutics (NASDAQ: SAGE), a biopharmaceutical company developing novel medicines to treat life-altering central nervous system (CNS) disorders, today announced that the U.S. Drug Enforcement Administration (DEA) has placed ZULRESSO™ (brexanolone) injection into Schedule IV . PRESS RELEASES. SAGE THERAPEUTICS' : Price Target From RBC Cut to $60 From $84; Survey Suggests .. All news about SAGE THERAPEUTICS, INC. AXSOME THERAPEUTICS : says U.S. FDA asks for no extra data for depression drug, .. SAGE THERAPEUTICS : Insider Makes Significant Stock buy in Sage Therapeutics (SA.. These forward-looking statements are neither promises nor guarantees of future performance, and are subject to a variety of risks and uncertainties, many of which are beyond Sage’s control, which could cause actual results to differ materially from those contemplated in these forward-looking statements, including the risks that: the proposed transaction may not be completed in a timely manner or at all; certain closing conditions to the proposed transaction may not be satisfied; the anticipated benefits of the proposed collaboration may never be achieved; results from interim data cuts from a clinical study may not be reflective of the results that will be achieved in the full study once completed; success in non-clinical studies or in earlier clinical trials may not be repeated or observed in ongoing or future studies, and ongoing and future non-clinical and clinical results may not meet their primary or key secondary endpoints or be sufficient to file for or gain regulatory approval to market a product without further development work or may not support further development at all; adverse results may occur at any stage of development that negatively impact further development or that require additional nonclinical and clinical work which may not yield positive results; different or more severe adverse events may occur at the higher doses of zuranolone or SAGE-324 currently being studied; issues may arise with the efficacy or durability of short-term treatment, or co-initiated treatment with zuranolone or there may be safety and efficacy concerns with respect to retreatment with zuranolone or chronic treatment with SAGE-324 that require additional nonclinical studies or clinical trials be conducted; delays in initiation of dosing or conduct or completion of ongoing and planned clinical trials may occur that may impact expected timelines; COVID-19 may impact clinical development timelines; the FDA may ultimately decide that the design or results of completed and planned clinical trials for zuranolone or SAGE-324, even if positive, are not sufficient for regulatory approval in the indications that are the focus of our development plan; the actual size of the MDD, PPD and essential tremor patient populations may be significantly lower than estimates; Sage may not obtain the operational, strategic or financial flexibility or value creation opportunities it expects from the collaboration with Biogen; there may be other unexpected hurdles in the development and manufacture of zuranolone or SAGE-324 which may delay or impact planned activities or results; as well as those risks more fully discussed in the section entitled “Risk Factors” in Sage’s most recent Quarterly Report on Form 10-Q, as well as discussions of potential risks, uncertainties, and other important factors in our subsequent filings with the Securities and Exchange Commission. 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