US2023382989A1PendingUtilityA1
Treatment for neoplastic diseases
Est. expiryAug 23, 2030(~4.1 yrs left)· nominal 20-yr term from priority
Inventors:John Simard
C07K 2317/92A61P 35/04A61P 35/00A61K 2039/505C07K 16/245A61K 39/395C07K 2317/76A61P 1/00A61P 11/00A61P 11/02A61P 11/04A61P 25/00A61P 29/00A61P 35/02A61P 7/10
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Claims
Abstract
Administration of a mAb that specifically binds IL-1α is useful for treating tumor-associated diseases in human subjects.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of stabilizing a progressive cancer in a human patient having cancer that has progressed after treatment with chemotherapy, radiotherapy, or biologic agents, the method comprising the step of repeatedly administering to the subject a pharmaceutical composition comprising a pharmaceutically acceptable carrier and an anti-interleukin-1alpha (anti-IL-1α) antibody at least until the progression of the cancer has been stabilized.
2 . The method of claim 1 , wherein the human patient's progressive cancer is metastatic, and the step of repeatedly administering the pharmaceutical composition results in a decrease in the tumor burden in the patient.
3 . The method of claim 1 , wherein the progressive cancer is metastatic colorectal cancer.
4 . The method of claim 2 , wherein the progressive cancer is metastatic colorectal cancer.
5 . The method of claim 1 , wherein the progressive cancer is metastatic non-small cell lung cancer.
6 . The method of claim 2 , wherein the progressive cancer is metastatic non-small cell lung cancer.
7 . A method of reducing the size of a tumor in a human patient with nasopharyngeal carcinoma that was previously treated with chemotherapy, radiotherapy, or biologic agents, the method comprising the step of repeatedly administering to the subject a pharmaceutical composition comprising a pharmaceutically acceptable carrier and an anti-IL-1α antibody at least until the size of the tumor is reduced.
8 . The method of claim 7 , wherein the patient has at least one symptom selected from the group consisting of fatigue, fever, sweats, and ascites, and the step of repeatedly administering the pharmaceutical composition results in a decrease in the at least one symptom.
9 . A method of stabilizing Castleman's disease in a human patient, the method comprising the step of repeatedly administering to the subject a pharmaceutical composition comprising a pharmaceutically acceptable carrier and an anti-IL-1α antibody at least until the progression of the Castleman's disease has been stabilized.Join the waitlist — get patent alerts
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