Methods and compositions for treating melanoma
US-2024424002-A1 · Dec 26, 2024 · US
US12539340B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12539340-B2 |
| Application number | US-202217883434-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 8, 2022 |
| Priority date | Aug 6, 2021 |
| Publication date | Feb 3, 2026 |
| Grant date | Feb 3, 2026 |
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The invention provides compositions and methods for treating cancers and proliferative disorders, including solid tumor cancers and non-myeloid hematological malignancies, using radioconjugates targeting CD33, alone or in combination with one or more radioconjugates targeting other cancer-associated targets such as DR5, 5T4, HER2, HER3, and TROP2, antibody drug conjugates targeting these or other cancer-associated targets, therapeutic antibodies targeting these or other cancer-associated targets, chemotherapy agents and regimens, and immune checkpoint inhibitors.
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What is claimed is: 1 . A method for treating a solid tumor cancer or solid tumor premalignancy in a mammalian subject not afflicted with a myeloid-derived hematological cancer or myeloid-derived hematological premalignancy, comprising: administering a therapeutically effective amount of a 225 Ac-labeled conjugate of p-SCN-Bn-DOTA and lintuzumab to the mammalian subject. 2 . The method of claim 1 , wherein the solid tumor cancer or solid tumor premalignancy comprises ovarian cancer, non-small cell lung carcinoma, head and neck squamous cell cancer, pancreatic cancer, renal cancer, breast cancer, metastatic breast cancer, tamoxifen-sensitive tamoxifen-resistant breast cancer, triple negative breast cancer, prostate cancer, castration-resistant prostate cancer (CRPC), pancreatic cancer, small cell lung carcinoma (SCLC), non-small cell lung carcinoma (NSCLC), hepatocellular carcinoma (HCC), cholangiocarcinoma, gastric cancer, colorectal cancer, esophageal cancer, or Barrett's esophagus. 3 . The method of claim 2 , wherein the mammalian subject is a human patient. 4 . The method of claim 3 , wherein the human patient is afflicted with a solid tumor cancer. 5 . The method of claim 1 , further comprising administering at least one immune checkpoint inhibitor to the mammalian subject. 6 . The method of claim 5 , wherein the at least one immune checkpoint inhibitor comprises one or both of a PD-1 and PD-L1 inhibitor. 7 . The method of claim 6 , wherein the mammalian subject is a human patient. 8 . The method of claim 7 , wherein the human patient is afflicted with a solid tumor cancer. 9 . The method of claim 5 , wherein the at least one immune checkpoint inhibitor comprises a CTLA-4 inhibitor. 10 . The method of claim 9 , wherein the mammalian subject is a human patient. 11 . The method of claim 10 , wherein the human patient is afflicted with a solid tumor cancer. 12 . The method of claim 5 , wherein the mammalian subject is a human patient. 13 . The method of claim 12 , wherein the human patient is afflicted with a solid tumor cancer. 14 . The method of claim 1 , wherein the solid tumor cancer or solid tumor premalignancy is a CD33 low-expressing or CD33-negative solid tumor cancer or CD33 low-expressing or CD33-negative solid tumor premalignancy. 15 . The method of claim 14 , wherein the mammalian subject is a human patient. 16 . The method of claim 15 , wherein the human patient is afflicted with a solid tumor cancer. 17 . The method of claim 1 , wherein the mammalian subject is a human patient. 18 . The method of claim 17 , wherein the human patient is afflicted with a solid tumor cancer.
Antineoplastic agents · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
against receptors, cell-surface antigens or cell-surface determinants · CPC title
characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin · CPC title
comprising antibodies · CPC title
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