Company Overview of Karuna Pharmaceuticals Inc
Karuna Pharmaceuticals Inc., a clinical-stage pharmaceutical company, targets muscarinic receptors for the treatment of CNS disorders. The company offers KarXT that targets the muscarinic system for the treatment of schizophrenia and is composed of xanomeline, a novel clinical-stage muscarinic acetylcholine receptor agonist (activator); and trospium chloride, an FDA-approved muscarinic receptor antagonist (blocker) that has been shown not to enter the central nervous system. Its KarXT controls psychosis. The company was incorporated in 2009 and is based in Boston, Massachusetts. Karuna Pharmaceuticals Inc. operates as a subsidiary of PureTech Health plc.
501 Boylston Street
Boston, MA 02116
Founded in 2009
Key Executives for Karuna Pharmaceuticals Inc
Founder, Chief Executive Officer, President and Director
Compensation as of Fiscal Year 2017.
Karuna Pharmaceuticals Inc Key Developments
Karuna Pharmaceuticals Announces Positive Results from Tolerability Proof-Of-Concept Study of KarXT
Dec 15 16
Karuna Pharmaceuticals announced positive results from a tolerability proof-of-concept study of its proprietary product, KarXT. In the study, KarXT (xanomeline plus trospium chloride), which is being developed as a novel antipsychotic for schizophrenia and Alzheimer's disease, was found to be generally well-tolerated and have superior tolerability to xanomeline alone. Based on these positive safety results and previous efficacy data on xanomeline, Karuna intends to initiate a Phase 2 clinical trial of KarXT in 2017. KarXT was shown to reduce the incidence of prespecified cholinergic adverse events by a statistically significant and clinically meaningful extent (46% p=0.016). KarXT combines xanomeline, a novel clinical-stage muscarinic acetylcholine receptor agonist, with trospium chloride, a muscarinic antagonist, and is being developed to selectively target muscarinic receptors in the CNS. Exclusively licensed to Karuna, xanomeline has demonstrated robust efficacy in reducing psychosis in both schizophrenia and Alzheimer's disease in previous studies, however, it has been associated with side effects that have limited its development. The results of the KarXT proof-of-concept study indicate that the addition of trospium chloride results in improved tolerability of xanomeline. Based on these positive safety results and previous efficacy data on xanomeline, Karuna intends to initiate a Phase 2 clinical trial of KarXT in 2017.
Karuna Pharmaceuticals Announces Dosing of the First Subject in Tolerability Proof-Of-Concept Study of its Proprietary Lead Product KarXT
Sep 12 16
Karuna Pharmaceuticals announced the dosing of the first subject in a tolerability proof-of-concept study of its proprietary lead product KarXT (xanomeline plus trospium chloride). The study, which will be conducted in up to 70 healthy individuals, aims to evaluate the tolerability of KarXT compared to xanomeline alone. Exclusively licensed to Karuna, xanomeline is a novel, muscarinic acetylcholine receptor agonist that has demonstrated robust efficacy in treating schizophrenia and psychosis in Alzheimer’s disease; however, it has also been associated with tolerability issues that have hindered its development. In a double-blind, placebo-controlled, monotherapy study in people with schizophrenia, a statistically significant, 24-point reduction over placebo was observed on the Positive and Negative Syndrome Scale (PANSS), a standard tool used to measure symptom severity in people with schizophrenia. By selectively targeting muscarinic receptors in the CNS with the KarXT approach, Karuna aims to reduce the peripheral cholinergic side effects previously seen with xanomeline alone. The randomized, double-blind, multiple-dose study will dose up to 70 healthy volunteers aged 18 to 60 for in-clinic treatment over the course of nine days. Following a two-day run-in period with trospium alone, subjects will receive xanomeline with either trospium chloride or placebo. Top-line results are expected by the end of 2016.
Karuna Pharmaceuticals Appoints Atul Pande to its Board
Jul 29 16
Karuna Pharmaceuticals announced the appointment of Atul Pande, M.D., to its Board of Directors. Dr. Pande brings to Karuna more than 25 years of experience in the fields of psychiatry and neurosciences and an expertise in drug development. Dr. Pande has more than two decades of experience in drug development. Dr. Pande is the former Senior Vice President, Head of Neuroscience, and Senior Advisor, Pharmaceutical R&D at GlaxoSmithKline. Dr. Pande has been active in the development of multiple important central nervous system drugs while holding various senior roles in Pfizer R&D, Parke-Davis/Warner-Lambert, and Lilly Research Laboratories. His experience includes drug development, registration, launch and lifecycle management in the areas of anxiety, depression, epilepsy, neuropathic pain, schizophrenia, traumatic brain injury, and Alzheimer's and Parkinson's diseases.
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