Complement component C5 antibodies
US-9701743-B2 · Jul 11, 2017 · US
US9932395B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9932395-B2 |
| Application number | US-201715645022-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 10, 2017 |
| Priority date | Feb 20, 2014 |
| Publication date | Apr 3, 2018 |
| Grant date | Apr 3, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present disclosure relates to antibodies and polynucleotides encoding the same, that may be used to prevent, control, or reduce the activity of the complement pathway. In addition, the disclosure is directed to compositions and methods for diagnosing and treating diseases mediated by or involving complement C5. Specifically, the disclosure is related to C5 antibodies.
Opening claim text (preview).
We claim: 1. A nucleic acid molecule encoding an anti-C5 antibody, wherein the antibody binds to C5 and inhibits complement dependent hemolysis, but does not block C5a formation, wherein the antibody comprises a first amino acid sequence and a second amino acid sequence, further wherein: (a) the first sequence comprising: (i) a CDR1 selected from the group consisting of SEQ ID NOs:13, 19, 25, 31, 37 and 43; (ii) a CDR2 selected from the group consisting of amino acids sequence GTS (SEQ ID NOS: 14 and 20), SGS (SEQ ID NO: 26), RTS (SEQ ID NO: 32), YTS (SEQ ID NO: 38), and WAS (SEQ ID NO: 44); and (iii) a CDR3 selected from the group consisting of SEQ ID NOs:15, 21, 27, 33, 39 and 45; and (b) the second sequence comprising: (i) a CDR1 selected from the group consisting of SEQ ID NOs:16, 22, 28, 34, 40 and 46; (ii) a CDR2 selected from the group consisting of SEQ ID NOs:17, 23, 29, 35, 41 and 47; and (iii) a CDR3 selected from the group consisting of SEQ ID NOs:18, 24, 30, 36, 42 and 48. 2. The nucleic acid molecule according to claim 1 , wherein the nucleic acid molecule is operably linked to a control sequence.
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Ophthalmic agents · CPC title
Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title
containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title
against material from animals or humans · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.