NeuBase Therapeutics, Inc.: Diferență între versiuni
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Admin (discuție | contribuții) (Pagină nouă: Pagina dedicata companiei NeuBase Therapeutics, Inc. listata cu simbolul US.NBSE ==Descriere companie== NeuBase Therapeutics, Inc. (https://www.neubasetherapeutics.com/) is a pre-clinical-stage biopharmaceutical company. The Company is focused on developing therapies to treat rare genetic diseases and cancers caused by mutant genes. The Company’s peptide-nucleic acid antisense oligonucleotide (PATrOL) platform focuses on addressing Huntington's disease (HD) and myotonic dy...) |
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==Descriere companie== | ==Descriere companie== | ||
NeuBase Therapeutics, Inc. (https://www.neubasetherapeutics.com/) is a pre-clinical-stage biopharmaceutical company. The Company is focused on developing therapies to treat rare genetic diseases and cancers caused by mutant genes. The Company’s peptide-nucleic acid antisense oligonucleotide (PATrOL) platform focuses on addressing Huntington's disease (HD) and myotonic dystrophy, as well as other genetic disorders. Its programs include NT0100, a PATrOL-enabled therapeutic program for systemic administration to target the mutant expansion in the HD messenger ribonucleic acid (mRNA) and NT0200, a PATrOL-enabled therapeutic program for systemic administration to target the mutant expansion in the myotonic dystrophy type one disease mRNA. | NeuBase Therapeutics, Inc. (https://www.neubasetherapeutics.com/) is a pre-clinical-stage biopharmaceutical company. The Company is focused on developing therapies to treat rare genetic diseases and cancers caused by mutant genes. The Company’s peptide-nucleic acid antisense oligonucleotide (PATrOL) platform focuses on addressing Huntington's disease (HD) and myotonic dystrophy, as well as other genetic disorders. Its programs include NT0100, a PATrOL-enabled therapeutic program for systemic administration to target the mutant expansion in the HD messenger ribonucleic acid (mRNA) and NT0200, a PATrOL-enabled therapeutic program for systemic administration to target the mutant expansion in the myotonic dystrophy type [[one]] disease mRNA. | ||
==Grafic actiuni companie== | ==Grafic actiuni companie== | ||