Zogenix to Release Third Quarter 2021 Financial Results and Host Conference Call and Webcast on November 4
Zogenix (NASDAQ: ZGNX) announced it will report its third-quarter financial results for the period ending September 30, 2021, on November 4, 2021, at 4:30 PM Eastern Time. A conference call will follow, providing updates on the company's ongoing research in rare diseases, including therapies for conditions like Dravet syndrome and Lennox-Gastaut syndrome. Zogenix has received approvals for its first therapy, FINTEPLA, in both the U.S. and Europe, with additional late-stage programs underway and plans for further research into genetic epilepsies.
- Zogenix has successfully developed FINTEPLA, approved by the U.S. FDA and the European Medicines Agency.
- The company is advancing late-stage development programs targeting rare diseases, including Lennox-Gastaut syndrome and TK2 deficiency.
- Plans to initiate studies of FINTEPLA in CDKL5 Deficiency Disorder (CDD) indicate potential growth avenues.
- None.
EMERYVILLE, Calif., Oct. 21, 2021 (GLOBE NEWSWIRE) -- Zogenix (NASDAQ: ZGNX), a global biopharmaceutical company developing rare disease therapies, today announced data that it will report its financial results for the third quarter ended September 30, 2021 and host a corporate update conference call and webcast after the market close on Thursday, November 4, 2021, at 4:30 PM Eastern Time.
Conference Call Details | |
Thursday, November 4, at 4:30 PM Eastern Time / 1:30 PM Pacific Time | |
Toll Free: | 855-327-6838 |
International: | 604-235-2082 |
Conference ID: | 10016695 |
Webcast: | http://public.viavid.com/index.php?id=146849 |
About Zogenix
Zogenix is a global biopharmaceutical company committed to developing and commercializing therapies with the potential to transform the lives of patients and their families living with rare diseases. The company’s first rare disease therapy, FINTEPLA® (fenfluramine) oral solution, has been approved by the U.S. FDA and the European Medicines Agency and is in development in Japan for the treatment of seizures associated with Dravet syndrome, a rare, severe lifelong epilepsy. The company has two additional late-stage development programs: one in a rare epilepsy called Lennox-Gastaut syndrome and one in a mitochondrial disease called TK2 deficiency. Zogenix also plans to initiate a study of FINTEPLA in a genetic epilepsy called CDKL5 Deficiency Disorder (CDD) and is collaborating with Tevard Biosciences to identify and develop potential next-generation gene therapies for Dravet syndrome and other genetic epilepsies.
CONTACTS:
Zogenix
corpcomms@zogenix.com
Investors
Brian Ritchie
Managing Director, LifeSci Advisors LLC
+1 (212) 915-2578 | britchie@lifesciadvisors.com
Media
Trish McCall, Porter Novelli
+1 (805) 390-3279 | trish.mccall@porternovelli.com
FAQ
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