US2023265206A1PendingUtilityA1
Antibodies against cdcp1 for the treatment and detection of cancer
Est. expiryOct 25, 2037(~11.2 yrs left)· nominal 20-yr term from priority
G01N 33/5759A61K 47/68031C07K 16/2896A61K 47/6803A61K 47/6849A61P 35/00C07K 16/2809G01N 33/57492C07K 2317/31C07K 2317/92G01N 2333/70596
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Claims
Abstract
The disclosure is related to antibodies and antibody fragments that specifically bind the CUB domain-containing protein 1 (CDCP1) and their methods and uses in treating and detecting cancers.
Claims
exact text as granted — not AI-modified1 - 22 . (canceled)
23 . A method for assessing CUB domain-containing protein 1 (CDCP1) expression, comprising:
(a) administering a radioisotope-labeled antibody or antibody fragment that specifically binds the CDCP1 ectodomain to a subject having pancreatic cancer; and (b) visualizing binding of the antibody or antibody fragment to cells of the subject to assess CDC1 expression, wherein the radioisotope is a positron-emitter, and the antibody or antibody fragment comprises light chain CDRs of SEQ ID NO:11, SEQ ID NO:13 and SEQ ID NO:20, and heavy chain CDRs of SEQ ID NO:17, SEQ ID NO:18, and SEQ ID NO:19.
24 . The method of claim 23 , wherein the antibody or antibody fragment comprises a heavy chain variable domain (VH) and a light chain variable domain (VL), and the VH comprises the amino acid sequence having at least 95% sequence identity to SEQ ID NO:57, and the VL comprises an amino acid sequence having at least 95% sequence identity to SEQ ID NO:58.
25 . The method of claim 23 , wherein the antibody or antibody fragment comprises a heavy chain variable domain (VH) and a light chain variable domain (VL), and the VH comprises the amino acid sequence of SEQ ID NO:57, and the VL comprises the amino acid sequence of SEQ ID NO:58.
26 . The method of claim 23 , wherein the positron-emitter is selected from the group consisting of 68 Ga, 18 F, 64 Cu, 86 Y, 76 Br, 89 Zr, and 124 I.
27 . The method of claim 26 , wherein the positron-emitter is 89 Zr.
28 . The method of claim 26 , wherein visualizing comprises use of positron emission tomography (PET).
29 . The method of claim 23 , wherein the pancreatic cancer is pancreatic adenocarcinoma.
30 . The method of claim 29 , wherein the pancreatic adenocarcinoma is a pancreatic ductal adenocarcinoma.
31 . A radioisotope-labeled antibody or antibody fragment that specifically binds CUB domain-containing protein 1 (CDCP1) ectodomain and comprises light chain CDRs of SEQ ID NO:11, SEQ ID NO:13 and SEQ ID NO:20, and heavy chain CDRs of SEQ ID NO:17, SEQ ID NO:18, and SEQ ID NO:19, wherein the radioisotope is a positron-emitter.
32 . The antibody or antibody fragment of claim 31 , wherein the antibody or antibody fragment comprises a heavy chain variable domain (VH) and a light chain variable domain (VL), and the VH comprises the amino acid sequence having at least 95% sequence identity to SEQ ID NO:57, and the VL comprises an amino acid sequence having at least 95% sequence identity to SEQ ID NO:58.
33 . The antibody or antibody fragment of claim 31 , wherein the antibody or antibody fragment comprises a heavy chain variable domain (VH) and a light chain variable domain (VL), and the VH comprises the amino acid sequence of SEQ ID NO:57, and the VL comprises the amino acid sequence of SEQ ID NO:58.
34 . The antibody or antibody fragment of claim 31 , wherein the positron-emitter is selected from the group consisting of 68 Ga, 18 F, 64 Cu, 86 Y, 76 Br, 89 Zr, and 124 I.
35 . The antibody or antibody fragment of claim 34 , wherein the positron-emitter is 89 Zr.Join the waitlist — get patent alerts
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