US2011105740A1PendingUtilityA1
Soluble tnf receptors and their use in treatment of disease
Assignee: SANTARIS PHARMA AS A DENMARK CORPPriority: Nov 10, 2005Filed: Aug 30, 2010Published: May 5, 2011
Est. expiryNov 10, 2025(expired)· nominal 20-yr term from priority
Inventors:Peter L. Sazani
C12N 2310/3231C12N 2310/321C12N 15/1138C12N 2310/315C07H 21/04C12N 15/113C07K 14/7151C07K 14/70578C12N 2310/11C12N 2310/346C12N 2320/33C12N 15/111A61K 38/00A61K 48/00Y02A50/30A61P 29/00
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Abstract
The present invention relates to tumor necrosis factor (TNF) antagonists and corresponding nucleic acids derived from tumor necrosis factor receptors (TNFRs) and their use in the treatment of inflammatory diseases. These proteins are soluble secreted decoy receptors that bind to TNF and prevent TNF from signaling to cells. In particular, the proteins are mammalian TNFRs that lack exon 7 and which can bind TNF and can act as a TNF antagonist.
Claims
exact text as granted — not AI-modified1 .- 56 . (canceled)
57 . An oligomer having a nucleoside sequence selected from the group consisting of: CCACAATCAGTCCTAG (SEQ ID NO: 14), CACAATCAGTCCTA (SEQ ID NO: 21) and ACAATCAGTCCT (SEQ ID NO: 23), having alternating 2′-deoxy- and 2′-O-4′-(methylene)-bicyclic-ribonucleosides, wherein the 5′-terminal nucleoside is a 2′-O-4′-(methylene)-bicyclic-ribonucleoside and the 3′-terminal nucleoside is a 2′-deoxyribonucleoside and wherein the internucleoside linkages are phosphorothioate linkages.Cited by (0)
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