US2022288221A1PendingUtilityA1
Anti-egfr antibodies and antibody drug conjugates
Est. expiryMar 21, 2034(~7.7 yrs left)· nominal 20-yr term from priority
C07K 2317/34C07K 16/3023A61K 47/6865C07K 2317/565C07K 16/30A61K 47/6857C07K 2317/24C07K 16/3046C07K 2317/73A61K 47/6847C07K 2317/56A61K 47/6863C07K 2317/76A61K 47/6849A61P 35/00C07K 2317/92A61K 2039/505C07K 2317/622A61K 47/6889C07K 16/3053A61K 47/6803A61K 47/6811A61K 47/6851C07K 16/2863C07K 14/00C07K 2317/21A61P 43/00A61K 2121/00A61K 47/68035A61K 47/68033A61K 47/68031
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Claims
Abstract
The invention relates to anti-epidermal growth factor (EGFR) antibodies and antibody drug conjugates (ADCs), including compositions and methods of using said antibodies and ADCs.
Claims
exact text as granted — not AI-modified1 . An anti-human epidermal growth factor receptor (anti-hEGFR) antibody comprising
a heavy chain CDR3 domain comprising the amino acid sequence set forth in SEQ ID NO: 12, a heavy chain CDR2 domain comprising the amino acid sequence set forth in SEQ ID NO: 11, and a heavy chain CDR1 domain comprising the amino acid sequence set forth in SEQ ID NO: 20; and a light chain CDR3 domain comprising the amino acid sequence set forth in SEQ ID NO: 28, a light chain CDR2 domain comprising the amino acid sequence set forth in SEQ ID NO: 27, and a light chain CDR1 domain comprising the amino acid sequence set forth in SEQ ID NO: 26, wherein the antibody is an IgG isotype.
2 . The antibody of claim 1 , wherein the antibody comprises a heavy chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 76, and a light chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 77.
3 . An anti-human epidermal growth factor receptor (anti-hEGFR) antibody comprising
a heavy chain CDR3 domain comprising the amino acid sequence set forth in SEQ ID NO: 22, a heavy chain CDR2 domain comprising the amino acid sequence set forth in SEQ ID NO: 3, and a heavy chain CDR1 domain comprising the amino acid sequence set forth in SEQ ID NO: 21; and a light chain CDR3 domain comprising the amino acid sequence set forth in SEQ ID NO: 31, a light chain CDR2 domain comprising the amino acid sequence set forth in SEQ ID NO: 30, and a light chain CDR1 domain comprising the amino acid sequence set forth in SEQ ID NO: 29, wherein the antibody is an IgG isotype.
4 . The antibody of claim 1 , wherein the antibody comprises a heavy chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 78, and a light chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 79.
5 . A method for treating a subject having cancer, comprising administering an effective amount of an antibody drug conjugate (ADC) comprising an anti-EGFR antibody conjugated to at least one auristatin, wherein the anti-EGFR antibody is an IgG isotype; comprises a heavy chain variable region comprising a CDR3 domain comprising the amino acid sequence set forth in SEQ ID NO: 12, a CDR2 domain comprising the amino acid sequence set forth in SEQ ID NO: 11, and a CDR1 domain comprising the amino acid sequence set forth in SEQ ID NO: 10; and comprises a light chain variable region comprising a CDR3 domain comprising the amino acid sequence set forth in SEQ ID NO: 8, a CDR2 domain comprising the amino acid sequence set forth in SEQ ID NO: 7, and a CDR1 domain comprising the amino acid sequence set forth in SEQ ID NO: 6.Join the waitlist — get patent alerts
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