US2022211806A1PendingUtilityA1

Method for promoting bone growth using activin-actriia antagonists

Assignee: ACCELERON PHARMA INCPriority: Nov 23, 2005Filed: Aug 24, 2021Published: Jul 7, 2022
Est. expiryNov 23, 2025(expired)· nominal 20-yr term from priority
A61P 19/08C07K 2319/35A61P 19/10A61P 19/00A61P 35/04C40B 30/04A61K 38/00C07K 19/00A61K 38/179A61P 35/00C07K 2319/32C07K 14/4702C07K 2319/70A61K 45/06A61P 43/00C07K 1/16C07K 14/575C07K 14/71C07K 2319/30A61K 38/17
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Claims

Abstract

In certain aspects, the present invention provides compositions and methods for promoting bone growth and increasing bone density.

Claims

exact text as granted — not AI-modified
We claim: 
     
         1 . A composition for therapeutic administration comprising a polypeptide and a pharmaceutically acceptable carrier, wherein the polypeptide comprises an amino acid sequence that is at least 95% identical to SEQ ID NO: 2. 
     
     
         2 . The composition of  claim 1 , wherein the polypeptide is at least 98% pure as determined by size exclusion chromatography. 
     
     
         3 . The composition of  claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 97% identical to SEQ ID NO: 2. 
     
     
         4 . The composition of  claim 3 , wherein the polypeptide comprises an amino acid sequence that is at least 99% identical to SEQ ID NO: 2. 
     
     
         5 . The composition of  claim 4 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 2. 
     
     
         6 . The composition of  claim 1 , wherein the polypeptide is glycosylated and has a mammalian glycosylation pattern. 
     
     
         7 . The composition of  claim 6 , wherein the polypeptide has a glycosylation pattern obtainable from a chinese hamster ovary (CHO) cell line. 
     
     
         8 . The composition according to  claim 1 , wherein the N-terminal amino acid is isoleucine. 
     
     
         9 . The composition of  claim 8 , wherein the N-terminus of the polypeptide is ILGRSTQE (SEQ ID NO: 11). 
     
     
         10 . The composition of  claim 1 , wherein the composition is substantially pyrogen free. 
     
     
         11 . The composition of  claim 1 , wherein the polypeptide further comprises a domain that enhances one or more of in vivo stability, in vivo half life, uptake/administration, tissue localization or distribution, formation of protein complexes, or purification. 
     
     
         12 . The composition of  claim 11 , wherein the domain is an immunoglobulin Fc domain. 
     
     
         13 . The composition of  claim 11 , wherein the domain is serum albumin. 
     
     
         14 . The composition of  claim 11 , wherein the serum half life of the polypeptide is greater than two weeks. 
     
     
         15 . The composition of  claim 14 , wherein the serum half life of the polypeptide is 20-30 days. 
     
     
         16 . The composition of  claim 1 , wherein the polypeptide has one or more of the following characteristics: (i) binds to an ActRIIa ligand with a K D  of at least 10 −7 M; and (ii) inhibits ActRIIa signaling. 
     
     
         17 . The composition of  claim 1 , wherein the polypeptide is soluble and binds activin A. 
     
     
         18 . The composition of  claim 17 , wherein the polypeptide is an antagonist of activin A. 
     
     
         19 . The composition of  claim 18 , wherein the composition promotes bone growth in vivo. 
     
     
         20 . A method for promoting bone growth comprising administering an effective amount of the composition of  claim 1 . 
     
     
         21 . The method according to  claim 20 , wherein the compositions is administered no more frequently than once per month. 
     
     
         22 . The method according to  claim 21 , wherein the composition is administered no more frequently than once every three months. 
     
     
         23 . The method according to  claim 22 , wherein the composition is administered no more frequently than once every six months.

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