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Eloxx Pharmaceuticals NASDAQ:ELOX Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons are point mutations that disrupt protein synthesis from messenger RNA. As a consequence, patients with premature stop codon diseases have reduced or eliminated protein production from the mutation bearing allele accounting for some of the most severe phenotypes in these genetic diseases. These premature stop codons have been identified in over 1,800 rare and ultra-rare diseases. Read-through therapeutic development is focused on extending mRNA half-life and increasing protein synthesis by enabling the cytoplasmic ribosome to read through premature stop codons to produce full-length proteins. Eloxx's lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx's preclinical candidate pool consists of a library of novel drug candidates designed to be eukaryotic ribosomal selective glycosides identified based on read-through potential. Eloxx also has preclinical programs focused on kidney diseases including autosomal dominant polycystic kidney disease, as well as rare ocular genetic disorders. Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ.
Location: 950 Winter St, Massachusetts, 02451-1424, US | Website: www.eloxxpharma.com | Industry: Research and Development in Biotechnology | Sector: Professional, Scientific, and Technical Services
Market Cap
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52 Wk Range
$ - $
Previous Close
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Open
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Day Range
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Volume
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Avg Volume
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Enterprise Value
13.95M
Cash
4.775M
Avg Qtr Burn
-4.498M
Short % of Float
0.77%
Insider Ownership
0.41%
Institutional Own.
19.59%
Qtr Updated
09/30/23
Drug Pipeline
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Drug & Indication | Stage & Event | Catalyst Date |
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ELX-02 Details Rare genetic disease, Alport Syndrome | Phase 2 Update | |
ELX-02 Details Lung disease, Cystic fibrosis, Glabellar lines | Phase 2 Update | |
ZKN-013 Details Rare genetic disease, Junctional epidermolysis bullosa, Recessive dystrophic epidermolysis bullosa | Phase 1 Data readout | |
ELX-02 Details Rare genetic disease | Failed Discontinued |