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Pulmocide Announces Expansion of Management Team CI
U.S. FDA approves UCB's drug for rare childhood epilepsy RE
Zogenix Completes $1.9 Billion Buyout by UCB; Shares Delisted From Nasdaq MT
UCB Closes Zogenix Acquisition for Nearly $1.9 Billion MT
Zogenix, Inc.(NasdaqGM:ZGNX) dropped from NASDAQ Composite Index CI
Zogenix, Inc.(NasdaqGM:ZGNX) dropped from S&P Pharmaceuticals Select Industry Index CI
Zogenix, Inc.(NasdaqGM:ZGNX) dropped from S&P TMI Index CI
Zogenix, Inc.(NasdaqGM:ZGNX) dropped from S&P Global BMI Index CI
UCB BioSciences, Inc. completed the acquisition of Zogenix, Inc.. CI
Zogenix, Inc.(NasdaqGM:ZGNX) dropped from NASDAQ Biotechnology Index CI
Northland Downgrades Zogenix to Market Perform From Outperform, Lifts Price Target to $27 From $26 MT
Zogenix Q4 Loss Narrows, Revenue Increases MT
Zogenix, Inc. Reports Earnings Results for the Fourth Quarter Ended December 31, 2021 CI
Zogenix, Inc. Reports Earnings Results for the Full Year Ended December 31, 2021 CI
Earnings Flash (ZGNX) ZOGENIX Posts Q4 Revenue $26.6M MT
Health Care Stocks Floundering Late in Wednesday Trading MT
JMP Securities Downgrades Zogenix to Market Perform From Market Outperform MT
Top Midday Gainers MT
Health Care Stocks Moderately Higher Wednesday Afternoon MT
Needham & Co Downgrades Zogenix to Hold From Buy MT
Guggenheim Downgrades Zogenix to Neutral From Buy, Adjusts Price Target to $28 From $35 MT
William Blair Downgrades Zogenix to Market Perform From Outperform MT
Zogenix Agrees to $1.9 Billion Takeover by UCB; Shares Surge MT
Wall Street Set for Recovery After Bond Yield-Induced Sell-Off MT
Health Care Stocks Edge Higher Premarket Wednesday MT
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Zogenix Inc is a United States-based biopharmaceutical company. The Company is engaged in the development and commercialization of therapies for rare diseases. It is primarily focused on developing and commercializing two therapeutic product opportunities: Fintepla and MT1621. Its first rare disease therapy, Fintepla is an oral solution, developed for the treatment of seizures associated with Dravet syndrome, a rare, devastating, severe lifelong epilepsy. The Company also has two late-stage development programs underway, one for Fintepla for the treatment of seizures associated with Lennox-Gastaut syndrome (LGS), a rare childhood-onset epilepsy. MT1621 is an investigational deoxynucleoside-combination substrate enhancement therapy in development for the treatment of TK2d, an inherited mitochondrial deoxyribonucleic acid depletion disease that predominantly affects children and is often fatal.
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