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Eloxx Pharmaceuticals, Inc. (ELOX)

OTC Markets EXMKT - OTC Markets EXMKT Delayed price. Currency in USD
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0.69000.0000 (0.00%)
At close: 04:00PM EDT
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Trade prices are not sourced from all markets
Previous close0.0000
Open0.6000
Bid0.6800 x 800
Ask0.7000 x 312300
Day's range0.5208 - 0.6600
52-week range0.2000 - 5.9900
Volume11,741
Avg. volume1,816
Market cap2.169M
Beta (5Y monthly)2.56
PE ratio (TTM)N/A
EPS (TTM)-8.8800
Earnings date09 Sept 2024 - 13 Sept 2024
Forward dividend & yieldN/A (N/A)
Ex-dividend dateN/A
1y target estN/A
  • GlobeNewswire

    Eloxx Pharmaceuticals Provides Pipeline and Financing Updates

    First two subjects dosed in Phase 1 clinical trial of ZKN-013; ZKN-013 is being developed for the potential treatment of rare dermatological and other diseases associated with nonsense mutations Positive written FDA feedback and guidance from a pre-Investigational New Drug Application (PIND) meeting provides pathway to IND application submission to initiate a Phase 2 clinical trial in the US with ELX-02 in patients with nonsense mutation alport syndrome (NMAS) Secured binding commitment for addi

  • GlobeNewswire

    Eloxx Pharmaceuticals Provides ELX-02 and ZKN-013 Program Updates

    ELX-02 Granted Orphan Drug Designation (ODD) from U.S. Food and Drug Administration (FDA) for Treatment of Alport Syndrome Pre-Investigational New Drug (IND) Meeting Requested with U.S. FDA for ELX-02 to Discuss Planned next Study In Nonsense Mutation Alport Syndrome Signed Global Licensing Partnership for ZKN-013 with Almirall Pharmaceuticals with $3M upfront and up to $470M in milestones and Tiered Royalties on Global Sales New Paper Published on Autosomal Dominant Polycystic Kidney Disease (A

  • GlobeNewswire

    Almirall and Eloxx Pharmaceuticals Enter into Exclusive Agreement to license ZKN-013 for rare dermatological diseases

    Almirall obtains exclusive global rights to develop and commercialize ZKN-013 for the treatment of rare dermatological and other diseases associated with nonsense mutationsZKN-013 is a phase I ready oral therapy designed to overcome nonsense mutations that cause a premature stop codon resulting in nonfunctional protein production for example in recessive Dystrophic Epidermolysis Bullosa (RDEB), Junctional Epidermolysis Bullosa (JEB) and familial adenomatous polyposis (FAP) BARCELONA, Spain and W