IP Library › Granted Patent US 12,214,012
Granted Patent B2
US 12,214,012 · App. 16/918,527 · Granted Feb 4, 2025

Combined preparations for the treatment of cancer

Inventor: Frederic Triebel (Versailles, FR)
Assignee: IMMUTEP S.A.S.
A61K38/1774A61K31/282A61K31/4745A61K31/555A61K45/06C07K14/70503C07K2319/30
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Quick Facts
Patent No.
US 12,214,012
App. No.
16/918,527
Granted
Feb 4, 2025
Kind
B2
Abstract

Combined preparations for the treatment of cancer are described. The combined preparations comprise: (a) LAG-3 protein, or a derivative thereof that is able to bind to MHC class II molecules; and (b) an anti-neoplastic agent, wherein the anti-neoplastic agent is a platinum-based anti-neoplastic agent or a topoisomerase I inhibitor. Methods for the treatment of cancer using the combined preparations are also described.

Claims (16)

1. A method of treating or ameliorating a cancer, which comprises:

administering to a subject in need of such treatment or amelioration an effective amount of:

a derivative of LAG-3 protein that is able to bind to MHC class II molecules, wherein the derivative comprises domains D1 and D2 of human LAG-3 protein, and wherein the derivative is fused to an Immunoglobulin Fc sequence; and

an anti-neoplastic agent, wherein the anti-neoplastic agent is a platinum-based anti-neoplastic agent or a topoisomerase I inhibitor; and

synergistically reducing tumor growth in the subject, the synergistic reduction of tumor growth being more than a sum of a reduction of tumor growth caused by administration to the subject of the derivative alone and the anti-neoplastic agent alone.

2. A method according to claim 1 , wherein the derivative and the anti-neoplastic agent are administered sequentially to the subject.

3. A method according to claim 1 , wherein the derivative is administered after the anti-neoplastic agent.

4. A method according to claim 2 , wherein the derivative and the anti-neoplastic agent are administered to the subject within 96 hours of each other.

5. A method according to claim 1 , wherein the derivative and the anti-neoplastic agent are co-administered to the subject.

6. A method according to claim 1 , wherein the derivative is administered to the subject at a dose which is a molar equivalent of 0.25-30 mg of LAG-3Ig fusion protein IMP321 per individual.

7. A method according to claim 1 , wherein a plurality of doses of the derivative is administered to the subject.

8. A method according to claim 1 , wherein a plurality of doses of the anti-neoplastic agent is administered to the subject.

9. A method according to claim 1 , wherein a dose of the derivative is administered before, with, or after each administration of two or more doses of the anti-neoplastic agent.

10. A method according to claim 1 , wherein the derivative comprises domains D1, D2, D3, and optionally D4 of human LAG-3 protein.

11. A method according to claim 1 , wherein the derivative of LAG-3 protein is IMP321.

12. A method according to claim 1 , wherein the anti-neoplastic agent is selected from the group consisting of oxaliplatin, carboplatin, and topotecan.

Priority Claims (1)
GB 1322626 · Dec 19, 2013 · national
Continuity (2)
Continuation 15105789
Related Publication 20200323957A1 · Oct 15, 2020
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