IP Library Granted Patent US 10,517,827
Granted Patent B2
US 10,517,827 · App. 15/575,284 · Granted Dec 31, 2019

Dry powder composition comprising long-chain RNA

Inventors: Fabian Johannes Eber (Stuttgart, DE); Benyamin Yazdan Panah (Tübingen, DE); Stefanie Sewig (Tübingen, DE); Thomas Ketterer (Gomaringen, DE); Thorsten Mutzke (Reutlingen, DE); Tilmann Roos (Kusterdingen, DE); Michael Sonntag (Tübingen, DE); Michael Wiggenhorn (München, DE); Katharina Kolland (Augsburg, DE)
Assignee: CureVac AG
A61K9/16A61K9/1682A61K39/145A61K48/005A61K48/0091A61P31/00A61P31/04A61P31/12A61P33/02A61P35/00A61P37/06A61P37/08A61K48/00A61K2039/53
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Quick Facts
Patent No.
US 10,517,827
App. No.
15/575,284
Granted
Dec 31, 2019
Kind
B2
Abstract

The present invention is directed to a storage-stable formulation of long-chain RNA. In particular, the invention concerns a dry powder composition comprising a long-chain RNA molecule. The present invention is furthermore directed to methods for preparing a dry powder composition comprising a long-chain RNA molecule by spray-drying. The invention further concerns the use of such a dry powder composition comprising a long-chain RNA molecule in the preparation of pharmaceutical compositions and vaccines, to a method of treating or preventing a disorder or a disease, to first and second medical uses of such a dry powder composition comprising a long-chain RNA molecule and to kits, particularly to kits of parts, comprising such a dry powder composition comprising a long-chain RNA molecule.

Claims (18)

1. A method for preparing a dry powder comprising a long-chain RNA molecule, wherein the method comprises the steps of:

a) providing a liquid comprising the long-chain RNA molecule,

b) spray-drying the liquid of step a) with a spray-drying device having a drying gas inlet and a drying gas outlet, wherein the drying gas has a temperature at the inlet of at least 85° C., wherein the drying gas has a temperature at the outlet of at least 50° C.,

wherein the dry powder has a residual moisture content of 7% (w/w) or less, wherein the long-chain RNA molecule is in a complex with a cationic or polycationic compound, and wherein the long-chain RNA molecule comprises at least 200 nucleotides.

2. The method according to claim 1 , wherein the liquid of step a) further comprises at least one excipient selected from a cryoprotectant, a lyoprotectant and a bulking agent.

3. The method according to claim 1 , wherein the liquid of step a) does not contain a lipid compound.

4. The method according to claim 1 , wherein the liquid of step a) comprises a spray-drying-compatible solvent.

5. The method according to claim 1 , wherein the liquid of step a) is atomized and a droplet resulting from the atomization of the liquid is characterized by a mass median aerodynamic diameter of 300 nm to 200 μm.

6. The method according to claim 1 , which comprises a plurality of particles.

7. The method according to claim 6 , wherein the median particle size in a volume weighted distribution of the resulting dried powder is at least 1 μm.

8. The method according to claim 6 , wherein the average sphericity of the particles in the resulting dried powder is in a range from 0.7 to 1.0.

9. The method according to claim 1 , wherein the long-chain RNA molecule is present in the form of a free long-chain RNA molecule, or in the form of a complex comprising the long-chain RNA molecule.

10. The method according to claim 1 , wherein the long-chain RNA molecule comprises more than 200 nucleotides.

11. The method according to claim 1 , wherein the long-chain RNA molecule comprises at least one modification.

12. The method according to claim 1 , wherein the liquid of step a) further comprises a suspending agent and/or an osmolality of about 200 mosmol/l to about 400 mosmol/l.

13. The method according to claim 5 , wherein at least a first pressure nozzle is used as an atomizer, optionally wherein the pressure is less than about 1 bar.

14. The method according to claim 1 , wherein (a) the method is performed on bulk material, or the method is performed continuously, and/or (b) the method is performed in an open cycle device, or the method is performed in closed cycle device.

15. The method of claim 1 , wherein the dry powder comprises an average particle size of 1 μm to 20 μm.

Assignments (3)
CHANGE OF NAME Recorded Feb 13, 2023
From: CUREVAC AG
To: CUREVAC SE
Reel/Frame 062718/0191 →
CHANGE OF NAME Recorded Feb 10, 2023
From: CUREVAC AG
To: CUREVAC SE
Reel/Frame 062703/0541 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2018
From: EBER, FABIAN JOHANNES; YAZDAN PANAH, BENYAMIN; SEWING, STEFANIE; KETTERER, THOMAS; MUTZKE, THORSTEN; ROOS, TILMANN; SONNTAG, MICHAEL; WIGGENHORN, MICHAEL; KOLLAND, KATHARINA
To: CUREVAC AG
Reel/Frame 046353/0903 →
Priority Claims (2)
EP 15001517 · May 20, 2015 · regional
WO PCT/EP2015/002019 · Oct 13, 2015 · international
Continuity (1)
Related Publication 20180147146A1 · May 31, 2018
Cited By (18)
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