US2014220013A1PendingUtilityA1
Method for the diagnosis and prognosis of malignant diseases
Est. expiryApr 8, 2022(expired)· nominal 20-yr term from priority
A61K 39/39558A61K 45/06C12Q 1/6886C07K 16/18A61P 35/00G01N 33/5005C12N 15/113A61K 38/00A61N 5/10G01N 33/5759C07K 14/47
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Claims
Abstract
Methods for the treatment of tumors and cancer by exploiting the surface expression of the usually nuclear-localized protein, nucleolin.
Claims
exact text as granted — not AI-modified1 - 17 . (canceled)
18 . A pharmaceutical composition for treating cancer in a subject, comprising a therapeutically effective amount to treat a tumor or cancer of an anti-nucleolin antibody and a pharmaceutically acceptable carrier, wherein the anti-nucleolin antibody is substantially non-immunogenic to human.
19 . The pharmaceutical composition of claim 18 , wherein the composition is in unit dosage form.
20 . The pharmaceutical composition of claim 18 , wherein the anti-nucleolin antibody is a monoclonal antibody.
21 . The pharmaceutical composition of claim 18 , wherein the pharmaceutical composition is an injectable formulation.
22 . The pharmaceutical composition of claim 18 , wherein the anti-nucleolin antibody is an artificial antibody.
23 . The pharmaceutical composition of claim 18 , wherein the anti-nucleolin antibody is an antibody fusion protein.
24 . The pharmaceutical composition of claim 18 , wherein the anti-nucleolin antibody is not an antibody fragment.
25 . The pharmaceutical composition of claim 18 , wherein the anti-nucleolin antibody is a human antibody.
26 . The pharmaceutical composition of claim 20 , wherein the anti-nucleolin antibody is a human monoclonal antibody.
27 . A method of treating cancer in a subject comprising:
administering to said subject a therapeutically effective amount of an anti-nucleolin antibody and a pharmaceutically acceptable carrier, to kill cancer cells, wherein said nucleolin antibody is substantially non-immunogenic to human.
28 . The method of claim 27 , further comprising administering to said subject a chemotoxic or chemotherapeutic agent.
29 . The method of claim 27 , further comprising treating said subject with radiation therapy.
30 . The methods of claim 28 wherein said chemotoxic or chemotherapeutic agent is selected from the group consisting of cyclophosphamide, etoposide, doxorubicin, methotrexate, vincristine, procabazine, prednisone, dexamethasone, tamoxifen citrate, carboplatin, cisplatin, oxaliplatin, 5-fluorouracil, camptothecin, zoledronic acid, Ibandronate and mytomicin.
31 . The method of claim 27 , further comprising treating said subject with radiation therapy.Cited by (0)
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