IP Library Granted Patent US 9,186,373
Granted Patent B2
US 9,186,373 · App. 13/977,453 · Granted Nov 17, 2015

SiRNA against Cbl-b and optionally IL-2 and IL-12 for use in the treatment of cancer

Inventors: Günther Lametschwandtner (Vienna, AT); Hans Loibner (Vienna, AT); Manfred Schuster (Schrick, AT); Isabella Haslinger (Vienna, AT); Sandra Seidl (Vienna, AT)
Assignee: Apeiron Biologics AG
A61K31/713A61K38/20A61K38/208A61K38/2013A61K38/212C12N15/1137C12Y603/02C12N2310/14
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Quick Facts
Patent No.
US 9,186,373
App. No.
13/977,453
Granted
Nov 17, 2015
Kind
B2
Abstract

The invention relates to a method for the immune activation of NK cells by the reduction or inhibition of the Cbl-b function in said cells. This stimulates the congenital immune system and thus permits the therapy of appropriate diseases.

Claims (11)

1. A method of treating cancer in a patient comprising administering at least one Cbl-b inhibitory nucleic acid further defined as an antisense oligonucleotide, siRNA, or shRNA, in combination with at least one NK cell-stimulatory substance further defined as at least one of the following combinations:

IL-2 and one or more of IL-12, IL-23, IFN-alpha, or IFN-beta, or any combination thereof; or

IFN-alpha and one or both of IL-15 or IL-21; or

IL-12 and one or both of IL-15 or IL-7.

2. The method of claim 1 , wherein the Cbl-b inhibitor and at least one further NK cell-stimulatory substance is administered in combination with at least one of an immune cell-stimulatory cytokine, an interferon or interferon stimulator, an antibody having an Fc domain, or a TLR or PAMP receptor ligand.

3. The method of claim 1 , wherein the Cbl-b inhibitor and at least one further NK cell-stimulatory substance is administered in combination with at least one of a cytokine of the common gamma-chain cytokine, a cytokine of both the adaptive and the innate immune system, an effector cell cytokine, a TLR receptor agonist, or a PAMP receptor agonist.

4. The method of claim 1 , wherein the at least one Cbl-b inhibitor and the at least one further NK cell-stimulatory substance are comprised in one or more pharmaceutically acceptable carrier.

5. The method of claim 4 , wherein the pharmaceutically acceptable carrier is suitable for intracellular administration in a patient.

6. The method of claim 5 , wherein the pharmaceutically acceptable carrier is a liposomal or microsomal formulation.

7. The method of claim 1 , wherein the patient is a mammal.

8. The method of claim 7 , wherein the patient is a human.

Assignments (3)
SECURITY INTEREST Recorded Dec 23, 2024
From: APEIRON BIOLOGICS GMBH
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 069669/0908 →
CHANGE OF NAME Recorded Dec 10, 2024
From: APEIRON BIOLOGICS AG
To: APEIRON BIOLOGICS GMBH
Reel/Frame 069584/0365 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 22, 2014
From: LAMETSCHWANDTNER, GÜNTHER; LOIBNER, HANS; SCHUSTER, MANFRED; HASLINGER, ISABELLA; SEIDL, SANDRA
To: APEIRON BIOLOGICS AG
Reel/Frame 032947/0152 →
Priority Claims (1)
EP 10197146 · Dec 28, 2010 · regional
Continuity (1)
Related Publication 20140010781A1 · Jan 9, 2014