US2009155285A1PendingUtilityA1
Tgf-beta binding antibodies
Est. expiryDec 23, 2025(expired)· nominal 20-yr term from priority
A61P 35/04A61P 9/00C07K 2317/55C07K 2317/24C07K 2317/76A61P 31/00C07K 2317/92C07K 2317/74C07K 16/22C07K 2317/52A61P 29/00A61K 2039/505C07K 2319/00A61P 35/00
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Claims
Abstract
The present invention provides very high affinity antibodies, or antigen-binding fragments thereof, that neutralize mature human TGF-β1, TGF-β2, and TGF-β3. The antibodies of the invention are useful for treating cell proliferative disorders in a mammal.
Claims
exact text as granted — not AI-modified1 - 11 . (canceled)
12 . A method of treating a cell proliferative disorder, comprising administering to a subject in need thereof an effective amount of a monoclonal antibody that binds TGF-Beta 1, 2, and 3, wherein each heavy chain variable region comprises the amino acid sequence shown in SEQ ID NO: 69, and each light chain variable region comprises the amino acid sequence shown in SEQ ID NO: 45.
13 . The method of claim 12 , wherein said cell proliferative disorder is selected from the group consisting of myelodysplastic syndrome/myeloproliferative disorder, breast cancer, prostate cancer, ovarian cancer, hepatocellular carcinoma, pancreatic cancer, multiple myeloma, colorectal cancer, hairy cell leukemia, chronic myelogenous leukemia, and acute myelogenous leukemia.
14 . A method of treating a cell proliferative disorder, comprising administering to a subject in need thereof an effective amount of a monoclonal antibody that binds TGF-Beta 1, 2, and 3, wherein each heavy chain comprises the amino acid sequence shown in SEQ ID NO: 81 and each light chain comprises the amino acid sequence shown in SEQ ID NO: 80.
15 . The method of claim 14 , wherein said cell proliferative disorder is selected from the group consisting of myelodysplastic syndrome/myeloproliferative disorder, breast cancer, prostate cancer, ovarian cancer, hepatocellular carcinoma, pancreatic cancer, multiple myeloma, colorectal cancer, hairy cell leukemia, chronic myelogenous leukemia, and acute myelogenous leukemia.Cited by (0)
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