- KINECT 4: A Phase 3, One-Year, Open-Label Trial of Valbenazine in Participants with Tardive Dyskinesia (T159)Hot Topics Session: Sunday, Dec. 3, 2:30-2:45 p.m.Poster Session: Tuesday, Dec. 5, 5:30-7:30 p.m.
- Effects of Valbenazine on Prolactin in Adults with Tardive Dyskinesia: Pooled Results from 3 Randomized, Double-Blind, Placebo-Controlled Trials (M149)Poster Session I: Monday, Dec. 4, 5:30-7:30 p.m.
- Can Presynaptic and Postsynaptic Monoaminergic Mechanisms Work Synergistically? Current Findings and Future Directions (T224)Poster Session II: Tuesday, Dec. 5, 5:30-7:30 p.m.
- Valbenazine in Tardive Dyskinesia of Older and Younger Adults: Pooled Results from 3 Randomized, Double-Blind, Placebo-Controlled Trials (W152)Poster Session III: Wednesday, Dec. 6, 5:30-7:30 p.m.
Important Safety InformationWarnings & PrecautionsSomnolence INGREZZA can cause somnolence. Patients should not perform activities requiring mental alertness such as operating a motor vehicle or operating hazardous machinery until they know how they will be affected by INGREZZA.QT ProlongationINGREZZA may prolong the QT interval, although the degree of QT prolongation is not clinically significant at concentrations expected with recommended dosing. INGREZZA should be avoided in patients with congenital long QT syndrome or with arrhythmias associated with a prolonged QT interval. For patients at increased risk of a prolonged QT interval, assess the QT interval before increasing the dosage. Adverse ReactionsThe most common adverse reaction (=5% and twice the rate of placebo) is somnolence. Other adverse reactions (=2% and >placebo) include: anticholinergic effects, balance disorders/falls, headache, akathisia, vomiting, nausea, and arthralgia. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit MedWatch at www.fda.gov/medwatch or call 1-800-FDA-1088. Please see INGREZZA full Prescribing Information at www.INGREZZA.com/HCP About Neurocrine Biosciences, Inc.Neurocrine Biosciences is a San Diego based biotechnology company focused on neurologic, psychiatric and endocrine related disorders. The Company markets INGREZZA ® (valbenazine) capsules in the United States for the treatment of adults with tardive dyskinesia. INGREZZA is a novel, selective vesicular monoamine transporter 2 (VMAT2) inhibitor, and is the first FDA approved product indicated for the treatment of adults with tardive dyskinesia. The Company's three late-stage clinical programs are: elagolix, a gonadotropin-releasing hormone antagonist for women's health that is partnered with AbbVie Inc.; opicapone, a novel, once-daily, peripherally-acting, highly-selective catechol-o-methyltransferase inhibitor under investigation as adjunct therapy to levodopa in Parkinson's patients; and INGREZZA, a novel, once-daily, selective VMAT2 inhibitor under investigation for the treatment of Tourette syndrome. Neurocrine Biosciences, Inc. news releases are available through the Company's website via the internet at http://www.neurocrine.com. Forward-Looking Statements In addition to historical facts, this press release contains forward-looking statements that involve a number of risks and uncertainties. These statements include, but are not limited to, statements related to the benefits to be derived from INGREZZA and whether results from INGREZZA's clinical trials are indicative of real-world results. Among the factors that could cause actual results to differ materially from those indicated in the forward-looking statements are: risks and uncertainties associated with Neurocrine's business and finances in general as well as risks and uncertainties associated with the commercialization of INGREZZA; risks that INGREZZA clinical trials results may not be predictive of real-world results or of results in subsequent clinical trials; risks and uncertainties relating to competitive products and technological changes that may limit demand for INGREZZA; risks associated with the Company's dependence on third parties for development and manufacturing activities related to INGREZZA and the ability of the Company to manage these third parties; risks that the FDA or other regulatory authorities may make adverse decisions regarding INGREZZA; risks that INGREZZA may be alleged to infringe upon the proprietary rights of third parties, or have unintended side effects, adverse reactions or incidents of misuse; and other risks described in the Company's periodic reports filed with the Securities and Exchange Commission, including without limitation the Company's Quarterly Report on Form 10-Q for the quarter ended September 30, 2017. The Company disclaims any obligation to update the statements contained in this press release after the date hereof.
View original content: http://www.prnewswire.com/news-releases/neurocrine-biosciences-to-present-new-long-term-data-evaluating-ingrezza-for-the-treatment-of-tardive-dyskinesia-at-the-american-college-of-neuropsychopharmacology-annual-meeting-300563877.htmlSOURCE Neurocrine Biosciences, Inc.