The data will be made available virtually at 9:00 AM EST on Friday, September 11, 2020. This product has received approval in the European Union under the tradename EPIDYOLEX® for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) or Dravet syndrome in conjunction with clobazam in patients two years and older and is under EMA review for the treatment of TSC. GW undertakes no obligation to update or revise the information contained in this press release, whether as a result of new information, future events or circumstances or otherwise. Made In NYC | “Our data demonstrate that many people have tried cannabis products to manage symptoms, supporting the need for research in this area.”, About the Cannabis Use Among People with MS: A 2020 NARCOMS Survey. Learn about EPIDIOLEX® (cannabidiol), the first prescription formulation of highly purified, plant-derived cannabidiol (CBD). About NabiximolsNabiximols is expected to enter pivotal Phase 3 development in the United States in the second half of 2020. 1 Sativex Oralmucosal Spray, SmPC, https://www.medicines.org.uk/emc/product/602. Nabiximols is known as Sativex® outside of the United States and is indicated in numerous countries as a treatment for symptom improvement in adult patients with moderate to severe spasticity due to multiple sclerosis (MS) who have not responded adequately to other anti-spasticity medication and who demonstrate clinically significant improvement in spasticity related symptoms during an initial trial of therapy.1 These approvals were based on multiple pivotal trials conducted in Europe.2 Sativex is currently not approved for any indication in the U.S. About GW Pharmaceuticals plc and Greenwich Biosciences, Inc.Founded in 1998, GW is a biopharmaceutical company focused on discovering, developing and commercializing novel therapeutics from its proprietary cannabinoid product platform in a broad range of disease areas.
There were no cases of Hy’s law observed and there were no deaths in the trial. “Nabiximols has the potential to offer people with MS-related spasticity the first rigorously tested and FDA-regulated cannabis medicine for the condition, which remains a significant unmet therapeutic need in the U.S., and we look forward to initiating our Phase 3 development program this year in pursuit of that goal.”. The first presentation (P1109) includes results from a post-hoc analysis of a Phase 3 clinical trial (GWSP0604) conducted in two phases (A & B) to assess the favorable safety profile and potential clinical efficacy of nabiximols in persons with MS-associated spasticity.
GW Pharmaceuticals receives Australian Therapeutic Goods Administration (TGA) approval for EPIDYOLEX® (cannabidiol) for the treatment of seizures in patients with two rare, severe forms of... Greenwich Biosciences to Share Results of Cannabis Use Survey Conducted with the North American Research Committee on Multiple Sclerosis (NARCOMS) at Joint ACTRIMS-ECTRIMS Meeting, MSVirtual2020, Greenwich Biosciences to Present Data on Safety and Efficacy of Nabiximols in Persons with Multiple Sclerosis-Associated Spasticity at the Joint ACTRIMS-ECTRIMS Meeting, MSVirtual2020, GW Pharmaceuticals Announces the Appointment of David Gryska to its Board of Directors, 10 High-Growth Stocks Every Young Investor Should Own, Better Cannabis Stock: Charlotte's Web vs. GW Pharmaceuticals, GW Pharmaceuticals to Present at Upcoming Investor Conferences, Stephen Schultz, VP Investor Relations (U.S.). © 2020 Insider Inc. and finanzen.net GmbH (Imprint). The U.S. commercial rights are owned by GW. The Company is also carrying out a Phase 3 trial in Rett syndrome and has a deep pipeline of additional cannabinoid product candidates, including nabiximols, for which the Company is advancing multiple late-stage clinical programs in order to seek FDA approval in the treatment of spasticity associated with multiple sclerosis and spinal cord injury, as well as for the treatment of PTSD.
The data will be made available virtually at 9:00 AM EST on Friday, September 11, 2020. TuberOus SClerosis registry to increase disease Awareness (TOSCA) - baseline data on 2093 patients. Early identification of refractory epilepsy.
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