IP Library › Granted Patent US 11,583,582
Granted Patent B2
US 11,583,582 · App. 16/274,466 · Granted Feb 21, 2023

Use of recombinant LAG-3 or the derivatives thereof for eliciting monocyte immune response

Inventor: Frederic Triebel (Versailles, FR)
Assignee: IMMUTEP
A61K39/39A61K31/337A61K31/704A61K31/7068A61K38/1774A61K39/0011A61K45/06C07K14/70503C07K16/00C07K16/30A61K2039/54A61K2039/545A61K2039/55516A61K2039/57A61K2039/585C07K2317/24C07K2317/732C07K2319/00C07K2319/40
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Quick Facts
Patent No.
US 11,583,582
App. No.
16/274,466
Granted
Feb 21, 2023
Kind
B2
Abstract

The present invention relates to the use of a recombinant LAG-3 or derivatives thereof in order to boost a monocyte-mediated immune response, in particular to elicit an increase in the number of monocytes in blood. This finds use in the development of novel therapeutic agents for the treatment of an infectious disease or cancer.

Claims (17)

1. A method of treating cancer in a human subject in need thereof, which comprises:

administering to the subject an effective amount of:

(i) a chemotherapy agent; and

(ii) IMP321;

wherein the IMP321 induces a systemic increase in the number of monocytes in blood of the subject, and elicits a systemic monocyte-mediated immune response;

wherein the IMP321 is administered to the subject at a dose of more than 6 mg; and

wherein the blood concentration of the IMP321 in the subject is greater than 1 ng/ml, for at least 24 hours after administration of the IMP321 to the subject.

2. The method of claim 1 , wherein the chemotherapy agent and the IMP321 are administered to the subject simultaneously, separately, or sequentially.

3. The method of claim 1 , wherein the IMP321 is administered 12 to 96 hours after administration of the chemotherapy agent.

4. The method of claim 1 , wherein the subject is treated without administration of any additional antigen.

5. The method of claim 1 , wherein the subject is administered an effective plurality of doses of the IMP321.

6. The method of claim 1 , wherein the cancer is metastatic breast cancer or metastatic renal cell cancer.

7. The method of claim 1 , wherein the chemotherapy agent is selected from the group consisting of taxanes, anthracyclines, and gemcitabine.

8. The method of claim 7 , wherein the chemotherapy agent is a taxane.

9. The method of claim 8 , wherein the taxane is paclitaxel.

10. The method of claim 1 , wherein the IMP321 is administered to the subject at a dose of more than 6.25 mg.

11. The method of claim 1 , wherein the IMP321 is administered to the subject at a dose of about 30 mg.

Priority Claims (1)
EP 07291214 · Oct 5, 2007 · regional
Continuity (3)
Division 15407864 · Jan 17, 2017
Continuation 12681068
Related Publication 20190175726A1 · Jun 13, 2019
Cited By (1)
US 12,673,088