US2021214427A1PendingUtilityA1
Compositions comprising an anti-c5 antibody
Est. expiryMay 11, 2025(expired)· nominal 20-yr term from priority
Inventors:Yi Wang
C07K 16/18C07K 2317/56A61P 35/00A61P 11/00A61K 2039/505A61P 11/06A61P 43/00C07K 2317/55A61P 29/00A61K 2039/54A61K 2039/544A61P 11/08A61K 2039/543C07K 2317/565A61P 9/14
72
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Claims
Abstract
The present application relates to methods and compositions employing an antibody that inhibits activation of the complement system and can be used to prevent or treat a pulmonary disease or condition.
Claims
exact text as granted — not AI-modified1 - 30 . (canceled)
31 . A pharmaceutical composition comprising an anti-C5 antibody, sodium phosphate, sodium chloride, and polysorbate 80, wherein the anti-C5 antibody comprises a variable light chain CDR1 comprising amino acid residues 26-36 of SEQ ID NO:1, a variable light chain CDR2 comprising amino acid residues 52-58 of SEQ ID NO:1, a variable light chain CDR3 comprising amino acid residues 91-99 of SEQ ID NO:1, a variable heavy chain CDR1 comprising amino acid residues 152-161 of SEQ ID NO:1, a variable heavy chain CDR2 comprising amino acid residues 176-192 of SEQ ID NO:1, and a variable heavy chain CDR3 comprising amino acid residues 225-237 of SEQ ID NO:1.
32 . The pharmaceutical composition of claim 31 , wherein the pH of the composition is between pH 6 and pH 8.
33 . The pharmaceutical composition of claim 32 , wherein the composition has physiologic osmolality.
34 . A pharmaceutical composition comprising an anti-C5 antibody, sodium phosphate, sodium chloride, and polysorbate 80, wherein the anti-C5 antibody comprises a heavy chain variable region comprising residue numbers 1-122 of SEQ ID NO: 2 and a light chain variable region comprising residue numbers 1-108 of SEQ ID NO: 3.
35 . The pharmaceutical composition of claim 34 , wherein the pH of the composition is between pH 6 and pH 8.
36 . The pharmaceutical composition of claim 35 , wherein the composition has physiologic osmolality.
37 . A pharmaceutical composition comprising between 1 and 30 mg/mL of an anti-C5 antibody, sodium phosphate, sodium chloride, and polysorbate 80, wherein the anti-C5 antibody comprises a variable light chain CDR1 comprising amino acid residues 26-36 of SEQ ID NO:1, a variable light chain CDR2 comprising amino acid residues 52-58 of SEQ ID NO:1, a variable light chain CDR3 comprising amino acid residues 91-99 of SEQ ID NO:1, a variable heavy chain CDR1 comprising amino acid residues 152-161 of SEQ ID NO:1, a variable heavy chain CDR2 comprising amino acid residues 176-192 of SEQ ID NO:1, and a variable heavy chain CDR3 comprising amino acid residues 225-237 of SEQ ID NO:1.
38 . The pharmaceutical composition of claim 37 , wherein the pH of the composition is between pH 6 and pH 8.
39 . The pharmaceutical composition of claim 38 , wherein the composition has physiologic osmolality.
40 . A pharmaceutical composition comprising between 1 and 30 mg/mL of an anti-C5 antibody, sodium phosphate, sodium chloride, and polysorbate 80, wherein the anti-C5 antibody comprises a heavy chain variable region comprising residue numbers 1-122 of SEQ ID NO: 2 and a light chain variable region comprising residue numbers 1-108 of SEQ ID NO: 3.
41 . The pharmaceutical composition of claim 40 , wherein the pH of the composition is between pH 6 and pH 8.
42 . The pharmaceutical composition of claim 41 , wherein the composition has physiologic osmolality.Join the waitlist — get patent alerts
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