US2016002630A1PendingUtilityA1

Bispecific Antisense Oligonucleotides that Inhibit IGFBP-2 and IGFBP-5 and Methods of Using Same

Assignee: UNIV BRITISH COLUMBIAPriority: Jan 17, 2002Filed: Jul 2, 2015Published: Jan 7, 2016
Est. expiryJan 17, 2022(expired)· nominal 20-yr term from priority
A61K 38/00C12N 2310/11A61K 31/713C12N 2310/51A61P 35/04C12N 2310/3519A61P 35/00C12N 15/113C07K 2319/00C12N 2310/111C12N 15/11A61K 48/00
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Claims

Abstract

Bispecific antisense oligonucleotides which consist essentially of a sequence of bases that is complementary to portions of both the gene encoding human IGFBP-2 and the gene encoding human IGFBP-5 are useful in as antisense therapeutics in the treatment of endocrine-regulated cancers.

Claims

exact text as granted — not AI-modified
1 - 18 . (canceled) 
     
     
         19 . A bispecific antisense oligodeoxynucleotide wherein the base sequence of the oligodeoxynucleotide consists of SEQ. ID NO. 5. 
     
     
         20 . A pharmaceutical composition comprising a bispecific antisense oligodeoxynucleotide and a pharmaceutically acceptable carrier, wherein the base sequence of the bispecific antisense oligodeoxynucleotide consists of SEQ ID NO. 5, and wherein the bispecific antisense oligonucleotide is present in the composition at a concentration of 50 nM or greater. 
     
     
         21 . The composition of  claim 20 , wherein the pharmaceutically acceptable carrier is a lipid carrier. 
     
     
         22 . The composition of  claim 20 , wherein the bispecific antisense oligodeoxynucleotide is present in the composition at a concentration of 50 to 500 nM. 
     
     
         23 . The composition of  claim 22 , wherein the pharmaceutically acceptable carrier is a lipid carrier.

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