Bispecific binding agents
US-9133272-B2 · Sep 15, 2015 · US
US9708375B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9708375-B2 |
| Application number | US-201414776917-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 14, 2014 |
| Priority date | Mar 15, 2013 |
| Publication date | Jul 18, 2017 |
| Grant date | Jul 18, 2017 |
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The present application is directed to avimers and peptides and various combinations thereof in addition to methods of making and using them.
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The invention claimed is: 1. A polypeptide comprising a non-naturally-occurring monomer domain capable of binding sclerostin, wherein the monomer domain comprises the amino acid sequence of DVAYAECMDSLEDVDYNCFLPEDQ (SEQ ID NO: 683). 2. The polypeptide according to claim 1 , with an affinity (K D ) to sclerostin of less than or equal to 1×10 −7 M. 3. The polypeptide according to claim 1 comprising a dimer of the monomer domain. 4. The polypeptide of claim 1 , further comprising a polypeptide having affinity to DKK1selected from Tables 16-19. 5. The polypeptide of any one of claims 1 , 2 , 3 , and 4 , further comprising a polyethylene glycol (PEG) conjugation or fusion. 6. A peptide fusion comprising a polypeptide comprising a non-naturally-occurring monomer domain capable of binding sclerostin fused to an antibody or fragment thereof, wherein the monomer domain comprises the amino acid sequence DVAYAECMDSLEDVDYNCFLPEDQ (SEQ ID NO: 683). 7. The peptide fusion claim 6 , wherein the polypeptide is fused to the heavy chain or the light chain of the antibody. 8. The peptide fusion of claim 6 , wherein the polypeptide comprises a dimer of the monomer domain. 9. The peptide fusion of claim 7 , 6 or 8 , wherein the polypeptide is fused to a human Fc. 10. The peptide fusion of claim 7 , 6 or 8 , wherein the antibody is an anti-DKK antibody.
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Human Necessities · mapped topic
from animals; from humans · CPC title
against material from animals or humans · CPC title
fusions, other than Fc, for prolonged plasma life, e.g. albumin · CPC title
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