IP Library Granted Patent US 10,729,785
Granted Patent B2
US 10,729,785 · App. 15/309,686 · Granted Aug 4, 2020

Particles comprising protamine and RNA in combination with endosome destabilizing agents

Inventor: Steve Pascolo (Zurich, CH)
Assignee: BioNTech SE
A61K48/0008A61K9/1694A61K38/1709A61K41/0057A61K47/32A61K47/42A61K47/585A61K47/645A61K47/6921C12N15/88C12N2760/16033C12N2760/16122C12N2760/16131Y02A50/463
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Quick Facts
Patent No.
US 10,729,785
App. No.
15/309,686
Granted
Aug 4, 2020
Kind
B2
Abstract

The present invention relates to particles comprising protamine, RNA and at least one endosome destabilizing agent, to methods of their production and to pharmaceutical compositions or kits containing the particles. It further relates to particles comprising protamine and RNA for use in methods of treatment or prevention of diseases and to kits comprising such particles together with at least one endosome destabilizing agent.

Claims (15)

1. A method of treating a disease or a method of immuno stimulation, comprising administering a particle to a subject in need thereof, wherein the particle comprises protamine 1000 or protamine 5000, RNA and at least one endosome destabilizing agent (EDA), wherein the EDA is a pH-reactive agent, wherein endosome destabilizing activity of the pH-reactive agent is triggered by exposure to a pH in the range of from 4.0 to 6.5, wherein the pH-reactive agent is selected from the group consisting of polymers and a peptide, wherein the polymers are polymers of acrylic acid or substituted acrylic acid and the peptide comprises influenza hemagglutinin peptide 2 according to SEQ ID NO: 2, and wherein the RNA is messenger RNA (mRNA).

2. The method of claim 1 , wherein the protamine:RNA mass ratio is in the range of from about 16:1 to 1:2.

3. The method of claim 1 , wherein the particle has a size in the range of from about 10 nm to 990 nm.

4. The method of claim 1 , wherein the polymer of acrylic acid or substituted acrylic acid is poly(2-propylacrylic acid).

5. The method of claim 1 , wherein the particle is administered in combination with another therapeutic agent, wherein the therapeutic agent is administrated prior to, simultaneously with, or after the administration of the particle.

6. The method of claim 1 , wherein the particle is administered by an administration route selected from the group comprising: intravenous, intraarterial, subcutaneous, in the lymph node, intradermal or intramuscular adminitrations.

7. The method of claim 1 , wherein the disease is a genetic disease.

8. The method of claim 7 , wherein the genetic disease is a myopathy.

9. The method of claim 1 , wherein the subject is human.

10. The method of claim 1 , wherein the method is for immunostimulation and the RNA encodes a disease associated antigen.

11. The method of claim 7 , wherein the genetic disease is cystic fibrosis.

12. The method of claim 1 , wherein the disease is cancer.

13. The method of claim 1 , wherein the disease is an infectious disease.

14. The method of claim 1 , wherein the disease is an allergy.

15. The method of claim 1 , wherein the disease is an autoimmune disease.

Assignments (2)
CHANGE OF NAME Recorded May 6, 2020
From: BIONTECH AG
To: BIONTECH SE
Reel/Frame 052595/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2017
From: PASCOLO, STEVE
To: BIONTECH AG
Reel/Frame 040959/0051 →
Continuity (1)
Related Publication 20170151349A1 · Jun 1, 2017