US2011027281A1PendingUtilityA1
Single domain antibodies directed against tumor necrosis factor-alpha and uses therefor
Est. expiryNov 8, 2022(expired)· nominal 20-yr term from priority
A61P 31/00A61P 37/06A61P 31/04A61P 35/00A61K 2039/505C07K 2317/569C07K 2317/31C07K 2317/76C07K 2317/24C07K 16/18C07K 2317/565C07K 16/2863A61P 19/02C07K 16/40C07K 16/4291C07K 2317/92C07K 16/2875C07K 2317/22C07K 2319/00C07K 16/241C07K 2317/626C07K 16/249C07K 2317/567C07K 16/36C07K 2317/34
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Claims
Abstract
The present invention relates to polypeptides derived from single domain heavy chain antibodies directed to Tumor Necrosis Factor-alpha. It further relates to single domain antibodies that are Camelidae VHHs. It further relates to methods of administering said polypeptides. It further relates to protocols for screening for agents that modulate the TNF-alpha receptor, and the agents resulting from said screening.
Claims
exact text as granted — not AI-modified1 . A composition comprising a first and a second anti-TNF-alpha antibody single variable domain and an anti-serum albumin antibody single variable domain, wherein said first and second anti-TNF-alpha antibody single variable domains have the same TNF-alpha epitope binding specificity.
2 . The composition of claim 1 , wherein said first and second anti-TNF-alpha antibody single variable domains are identical.
3 . The composition of claim 1 , wherein the anti-TNF-alpha antibody single variable domains have a monomer surface plasmon resonance K D of about 300 nM to about 5 pM.
4 . The composition of claim 3 , wherein said monomer surface plasmon resonance K D is about 50 nM to about 20 pM.
5 . The composition of claim 4 , wherein said monomer surface plasmon resonance K D is about 1 nM to about 100 pM.
6 . The composition of claim 1 , wherein said composition has at beta half-life of at least 24 hours.
7 . The composition of claim 1 , wherein said composition has at beta half-life of 12 hours to 48 hours.
8 . The composition of claim 1 , wherein said composition has at beta half-life of 12 hours to 26 hours.
9 . A composition comprising a first and a second anti-TNF-alpha antibody single variable domain and an anti-serum albumin antibody single variable domain, wherein said composition has at beta half-life of at least 12 hours.
10 . The composition of claim 9 , wherein said composition has at beta half-life of at least 24 hours.
11 . The composition of claim 9 , wherein said composition has at beta half-life of 12 hours to 48 hours.
12 . The composition of claim 9 , wherein said composition has at beta half-life of 12 hours to 26 hours.
13 . The composition of claim 9 , comprising one anti-serum albumin antibody single variable domain.
14 . The composition of claim 9 , wherein said first and second anti-TNF-alpha antibody single variable domains and said anti-serum albumin antibody single variable domains form a fusion polypeptide.
15 . The composition of claim 9 , wherein said first and second anti-TNF-alpha antibody single variable domains compete with TAR1-5-19 to bind TNF-alpha in an ELISA assay.
16 . The composition of claim 9 , wherein the anti-TNF-alpha antibody single variable domains have the same TNF-alpha epitope binding specificity.
17 . The composition of claim 9 , wherein said first and second anti-TNF-alpha antibody single variable domains are identical.
18 . The composition of claim 9 , wherein the anti-TNF-alpha antibody single variable domains have a monomer surface plasmon resonance K D of about 300 nM to about 5 pM.
19 . The composition of claim 18 , wherein said monomer surface plasmon resonance K D is about 50 nM to about 20 pM.
20 . The composition of claim 19 , wherein said monomer surface plasmon resonance K D is about 1 nM to about 100 pM.
21 . The composition of claim 9 , wherein each antibody single variable domain is linked to a polypeptide linker.
22 . The composition of claim 9 , wherein said first and second anti-TNF-alpha antibody single variable domain and said anti-serum albumin antibody single variable domain are linked.
23 . A kit comprising the composition of claim 9 , and instructions for its use.
24 . A pharmaceutical composition comprising the composition of claim 9 and a pharmaceutically acceptable carrier.Join the waitlist — get patent alerts
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