Business
Catalyst Pharmaceuticals to Report Second Quarter 2023 Financial Results on August 9, 2023
The Company to Host a Conference Call and Webcast on August 10, 2023, at 8:30 AM ET CORAL GABLES, Fla., July 24, 2023 (GLOBE NEWSWIRE) -- Catalyst
About this update from Catalyst Pharmaceuticals, Inc.
[{"type":"text","content":"The Company to Host a Conference Call and Webcast on August 10, 2023, at 8:30 AM ET\nCORAL GABLES, Fla., July 24, 2023 (GLOBE NEWSWIRE) -- Catalyst Pharmaceuticals, Inc. (\"Catalyst\") (Nasdaq: CPRX), a commercial-stage biopharmaceutical company focused on in-licensing, developing, and commercializing novel medicines for patients living with rare diseases, today announced that it will release its second-quarter 2023 financial results after market close on Wednesday, August 9, 2023. Catalyst's management team will host a conference call and webcast the following morning, Thursday, August 10, 2023, at 8:30 AM ET, to discuss the Company's financial results and provide a corporate update. Conference Call & Webcast Details Date/Time: August 10, 2023, at 8:30 AM ETUS/Canada Dial-in Number: (877) 407-8912International Dial-in Number: (201) 689-8059 The webcast will be accessible under the Investors section on the Company's website at www.catalystpharma.com. A replay of the webcast will be available on the Catalyst website for 30 days following the date of the event. About Catalyst PharmaceuticalsWith exceptional patient focus, Catalyst is committed to developing and commercializing innovative first-in-class medicines that address rare neurological and epileptic diseases. Catalyst’s flagship U.S. commercial product is FIRDAPSE® (amifampridine) Tablets 10 mg, approved for the treatment of Lambert-Eaton myasthenic syndrome (\"LEMS\") for adults and for children ages six to seventeen. In January 2023, Catalyst acquired the U.S. commercial rights to FYCOMPA® (perampanel) CIII, a prescription medicine approved in people with epilepsy aged four and older alone or with other medicines to treat partial-onset seizures with or without secondarily generalized seizures and with other medicines to treat primary generalized tonic-clonic seizures for people with epilepsy aged 12 and older. Further, Canada’s national healthcare regulatory agency, Health Canada, has approved the use of FIRDAPSE for the treatment of adult patients in Canada with LEMS. Further, on July 18, 2023, Catalyst acquired an exclusive license for North America for vamorolone, a promising best-in-class dissociative anti-inflammatory steroid treatment for Duchenne Muscular Dystrophy. Vamorolone has received FDA Orphan Drug and Fast Track designations and has been granted a PDUFA act...