US2008248049A1PendingUtilityA1
Treatment with anti-vegf antibodies
Est. expiryMay 30, 2023(expired)· nominal 20-yr term from priority
A61P 9/00A61P 35/00A61P 35/02A61P 35/04A61P 31/00A61P 43/00C07K 16/22A61K 39/3955C07K 2317/567A61K 39/39558A61K 45/06A61K 31/513A61K 31/337A61K 2039/505C07K 2317/24A61K 31/282A61K 31/4745C07K 16/3046A61K 31/573A61K 31/4545A61K 31/555A61K 31/525A61K 39/395A61K 9/0019A61K 31/519C07K 2317/21A61K 31/522A61K 39/39541A61K 31/7068C07K 2317/565A61K 38/50C07K 2317/76A61K 38/09A61K 38/212
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Claims
Abstract
This invention concerns in general treatment of diseases and pathological conditions with anti-VEGF antibodies. More specifically, the invention concerns the treatment of human patients susceptible to or diagnosed with cancer using an anti-VEGF antibody, preferably in combination with one or more additional anti-tumor therapeutic agents.
Claims
exact text as granted — not AI-modified1 . A method of treating leukemia in a human patient, comprising administering to the patient effective amounts of an anti-VEGF antibody and an anti-neoplastic composition, wherein the anti-VEGF antibody is bevacizumab or variants thereof and the anti-neoplastic composition comprises at least one chemotherapeutic agent.
2 . The method of claim 1 , wherein the leukemia is acute lymphoblastic leukemia (ALL), chronic myeloblastic leukemia, or hairy cell leukemia.
3 . The method of claim 1 , wherein the patient is previously untreated.
4 . The method of claim 1 , wherein the anti-VEGF antibody is administered to the patient at about 5 mg/kg to about 15 mg/kg every 2 to 3 weeks.
5 . The method of claim 1 , wherein the anti-VEGF antibody is administered to the patient by intravenous infusion over 30-90 mins.
6 . The method of claim 1 , further comprising administering to the patient a VEGF receptor antagonist selected from the group consisting of a VEGF variant, a soluble VEGF receptor fragment, an aptamer capable of blocking VEGFR, a neutralizing anti-VEGFR antibody, and a low molecule weight inhibitor of VEGFR tyrosine kinase.
7 . The method of claim 1 , further comprising administering to the patient an antagonist of Her2.
8 . The method of claim 1 , further comprising administering to the patient an antagonist of EGFR.
9 . The method of claim 1 , further comprising administering to the patient a cytokine.
10 . The method of claim 1 , wherein the chemotherapeutic agent is an anti-hormonal agent.Cited by (0)
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