US2020055953A1PendingUtilityA1
Method for Treating a GD2 Positive Cancer
Est. expiryJun 18, 2032(~5.9 yrs left)· nominal 20-yr term from priority
A61P 35/00A61P 43/00C07K 16/28C07K 2317/734C07K 14/55A61K 2039/505C07K 2317/732A61K 39/39558C07K 2319/00C07K 2317/24A61K 2039/54C07K 16/3084A61K 39/39533A61K 2039/545A61K 31/485C07K 2317/76A61K 45/06
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Abstract
Preparations and methods for treating a GD2 positive cancer by administering a preparation comprising an anti-GD2 antibody to a patient, wherein the patient is not concomitantly treated with Interleukin-2 (IL-2), and wherein one or more treatment periods with the antibody may be preceded, accompanied, and/or followed by one or more treatment periods with a retinoid.
Claims
exact text as granted — not AI-modified1 . A method of treating a GD2 positive cancer in a patient comprising administering an anti-GD2 antibody to the patient without concomitantly administering IL-2, wherein a GD2 positive cancer is treated in the patient.
2 . The method of claim 1 , further comprising treating the patient one or more times with a retinoid preceding, accompanying, and/or following administering of the anti-GD2 antibody.
3 . The method of claim 1 , wherein the anti-GD2 antibody is administered to the patient as a continuous infusion for one or more days and for two or more treatment cycles.
4 . The method of claim 1 , wherein the anti-GD2 antibody is not a 14G2a antibody.
5 . The method of claim 1 , wherein the anti-GD2 antibody is administered to the patient as a continuous infusion and the anti-GD2 antibody is not a 14G2a antibody.
6 . The method of claim 1 , wherein the patient is not concomitantly treated with GM-CSF.
7 . The method of claim 1 , wherein the patient is not concomitantly treated with a cytokine.
8 . The method of claim 7 , wherein the patient is not treated with IL-2, and/or GM-CSF, and/or a cytokine within the same treatment cycle and/or within the same overall treatment period.
9 . The method of claim 1 , wherein the GD2 positive cancer is neuroblastoma, high risk neuroblastoma, neuroblastoma stage 4, minimal residual neuroblastoma disease, relapsed neuroblastoma, and/or refractory neuroblastoma.
10 . The method of claim 1 , wherein the anti-GD2 antibody is ch14.18/CHO or ch14.18/SP2/0.
11 . The method of claim 1 , wherein the anti-GD2 antibody is administered in a daily dose of 10 or 25 mg/m 2 .
12 . The method of claim 1 , wherein the anti-GD2 antibody is administered for 4, 10, 14, 15, or 21 consecutive days.
13 . The method of claim 1 , wherein the anti-GD2 antibody is APN311 and is administered in a dose of 10 mg/m 2 /day for 10 consecutive days for 1, 2, 3, 4, 5, 6 or more treatment cycles.
14 . The method of claim 1 , wherein the anti-GD2 antibody is ch14.18/SP2/0 and is administered in a dose of 25 mg/m 2 /day for 4 consecutive days for 1, 2, 3, 4, 5 or more treatment cycles.
15 . The method of claim 1 , wherein the anti-GD2 antibody is administered as a continuous intravenous infusion over 24 hours per day.
16 . The method of claim 1 , wherein the administration of the anti-GD2 antibody is accompanied by the administration of a reduced dose of morphine and/or one or more other analgesic.Cited by (0)
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