428.83MMarket Cap-4766P/E (TTM)
8.530High8.140Low722.77KVolume8.380Open8.430Pre Close6.01MTurnover1.47%Turnover RatioLossP/E (Static)52.62MShares8.95052wk High13.21P/B401.75MFloat Cap3.89052wk Low--Dividend TTM49.29MShs Float418.400Historical High--Div YieldTTM4.63%Amplitude2.560Historical Low8.313Avg Price1Lot Size
Zevra Therapeutics Stock Forum
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⇨ ZYNRELEF® Vial Access Needle
‣ Postoperative pain
‣ PDUFA: 9/23/24 (sNDA)
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⇨ KarXT (xanomeline-trospium)
‣ Schizophrenia
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⇨ Dupixent
‣ Chronic obstructive pulmonary disease
‣ PDUFA: 9/27/24 (sBLA)
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⇨ Tislelizumab, KEYTRUDA, OPDIVO & YER...
Zevra Therapeutics to Present Top-Line Data from the Phase 2 Clinical Trial of KP1077 for Idiopathic Hypersomnia at Sleep Europe 2024
Zevra Therapeutics (NASDAQ: ZVRA) announced that top-line data from its Phase 2 clinical trial of KP1077 for idiopathic hypersomnia (IH) will be presented at Sleep Europe 2024. The trial (NCT05668754) was a placebo-controlled, double-blind, randomized withdrawal study evaluating the safety and tolerability of KP1077 (serdexmethylp...
Zevra Therapeutics’ MIPLYFFA™ (arimoclomol) Receives U.S. FDA Approval as Treatment for Niemann-Pick Disease Type C
Zevra Therapeutics announced FDA approval of MIPLYFFA™ (arimoclomol) as the first treatment for Niemann-Pick disease type C (NPC), an ultra-rare neurodegenerative disease. MIPLYFFA is indicated for use with miglustat to treat neurological manifestations in patients 2 years and older. The approval is based on a 12-month trial showing MIPLYFFA halted...
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