Zogenix (NASDAQ: ZGNX) was featured in a recent U.S. Equity Research Report published by Mizuho Securities USA LLC. The report reads, “We hosted a doc call last week with Dr. Kathryn Davis from UPenn Epilepsy Center to discuss Zogenix’s recent Lennox Gastaut (LGS) Phase 3 data. While the data looks underwhelming compared to Epidiolex on the surface, we believe FINTEPLA may ultimately have an edge in terms of durability, especially against Epidiolex where the dropout rate appears to be high. Dr. Davis estimates that she will try FINTEPLA for ~30% of her LGS patients. At the current price, we believe investors assign minimal credit to the LGS indication and we continue to see upside in the shares.”
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Zogenix, Inc. is a global pharmaceutical 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 has two late-stage development programs underway: FINTEPLA(R) (ZX008, fenfluramine oral solution) for the treatment of seizures associated with Dravet and Lennox-Gastaut syndromes, two rare and often-catastrophic childhood-onset epilepsies, and MT1621, a novel substrate enhancement therapy for the treatment of a rare genetic disorder called TK2 deficiency. For more information, visit the company’s website at www.Zogenix.com.
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