IP Library Patent Application 16375022
Patent Application
App. No. 16/375,022

Method for Treating a GD2 Positive Cancer

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Patent No.
US None
App. No.
16/375,022
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 (16)

1 . 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.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE NATURE OF CONVEYANCE FROM ASSIGNMENT TO LICENSE AGREEMENT PREVIOUSLY RECORDED AT REEL: 52321 FRAME: 294. ASSIGNOR(S) HEREBY CONFIRMS THE LICENSE AGREEMENT Recorded May 14, 2020
From: APEIRON BIOLOGICS AG
To: EUSA PHARMA (UK) LIMITED
Reel/Frame 052666/0575 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2020
From: LOIBNER, HANS; MUTSCHLECHNER, OLIVER; LADENSTEIN, RUTH; KLIER, ISABEL
To: APEIRON BIOLOGICS AG
Reel/Frame 052320/0973 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2020
From: APEIRON BIOLOGICS AG
To: EUSA PHARMA (UK) LIMITED
Reel/Frame 052321/0294 →