IP Library Granted Patent US 9,408,906
Granted Patent B2
US 9,408,906 · App. 13/153,826 · Granted Aug 9, 2016

Peptide particle formulation

Inventors: Reid M. Rubsamen (Alamo, CA); David Earl Heckerman (Santa Monica, CA)
Assignee: FLOW PHARMA, INC.
A61K39/39A61K9/1647A61K2039/55555
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Quick Facts
Patent No.
US 9,408,906
App. No.
13/153,826
Granted
Aug 9, 2016
Kind
B2
Abstract

A composition as disclosed is comprised of a plurality of groups of particles. The particles are comprised of a biocompatible polymer which maybe a co-polymer such as PLGA combined with a peptide of a sequence of interest, e.g. a sequence which corresponds to a sequence presented on a surface of a cell infected with a virus. A plurality of different groups of particles are provided in the formulation wherein the particles within any single group include peptides of identical amino acid sequence. The particles are sized such that they are sufficiently large so as to prevent more than the contents of a single particle from being presented to a single immune system cell.

Claims (29)

1. A composition, comprising a pharmaceutically acceptable carrier comprising monophosphoryl lipid A;

a first group of particles comprising a biocompatible polymer, and a first antigen consisting only of a single species consisting of eight to twenty amino acids embedded in the polymer; and

a second group of particles comprising a biocompatible polymer, and a second antigen consisting only of a single species consisting of eight to twenty amino acids embedded in the polymer, the second antigen being different from the first antigen;

wherein each particle in the first group and the second group is substantially spherical, and has a diameter such that only a single particle can be consumed by an antigen presenting cell in a range of from 10 microns ±20% to 25 microns ±20%.

2. The composition of claim 1 , further comprising:

a third group of particles comprising a biocompatible polymer, and a third antigen consisting only of a single species consisting of eight to twenty amino acids embedded in the polymer, the third antigen being different from both the first and second antigen.

3. The composition of claim 1 , wherein the biocompatible polymer is selected from the group consisting of poly(lactic-co-glycolic acid) (PLGA), polycaprolactone, polyglycolide, polylactic acid, poly-3-hydroxybutyrate.

4. The composition of claim 2 , further comprising:

a plurality of additional groups of particles with a diameter such that only a single particle can be consumed by an antigen presenting cell wherein additional antigens in each additional group are embedded in the polymer and are different from antigen in all other groups and the antigens of each group consisting only of a single species.

5. The composition of claim 4 , wherein all the particles of the composition are 12 microns to 22 microns in diameter ±20%.

6. A composition, comprising:

a pharmaceutically acceptable carrier comprising monophosphoryl lipid A;

a first group of particles comprising a biocompatible polymer, and a first antigen consisting only of a single species embedded in the polymer;

a second group of particles comprising a biocompatible polymer, and a second antigen consisting only of a single species embedded in the polymer, the second antigen being different from the first antigen; and

a third group of particles comprising a biocompatible polymer, and a third antigen consisting only of a single species embedded in the polymer, the third antigen being different from both the first and second antigen,

wherein each particle in the first group, second group and third group is substantially spherical, and has a diameter such that only a single particle can be consumed by an antigen presenting cell in a range of from 10 microns ±20% to 25 microns ±20%, and

wherein the biocompatible polymer is selected from the group consisting of poly(lactic co-glycolic acid) (PLGA), polycaprolactone, polyglycolide, polylactic acid, poly-3-hydroxybutyrate.

7. The composition of claim 6 , wherein the first, second and third antigens are each different antigens consisting of eight to twenty amino acids.

8. The composition of claim 6 , further comprising:

a plurality of additional groups of particles with a diameter such that only a single particle can be consumed by an antigen presenting cell wherein additional antigens in each additional group are embedded in the polymer and are different from the antigens in all other groups.

9. The composition of claim 8 , wherein all the particles of the composition are 12 microns to 22 microns in diameter ±20%.

10. The composition of claim 8 , wherein all the particles of the composition are 13 microns to 17 microns in diameter ±20%.

11. A composition, comprising:

a pharmaceutically acceptable carrier comprising monophosphoryl lipid A;

a first group of particles comprising a biocompatible polymer, and a first antigen consisting only of a single species consisting of eight to twenty amino acids embedded in the polymer; and

a second group of particles comprising a biocompatible polymer, and a second antigen consisting only of a single species consisting of eight to twenty amino acids embedded in the polymer, the second antigen being different from the first antigen;

a plurality of additional groups of particles with a diameter such that only a single particle can be consumed by an antigen presenting cell wherein additional antigens in each additional group are embedded in the polymer and are different from antigen in all other groups and the antigens of each group consisting only of a single species;

wherein each particle in the first group, the second group, and the additional groups, the diameter being substantially spherical, and has a diameter such that only a single particle can be consumed by an antigen presenting cell, the particle diameter being in a range of from 10 microns ±20% to 25 microns ±20%;

wherein the biocompatible polymer is selected from the group consisting of poly(lactic-co-glycolic acid) (PLGA), polycaprolactone, polyglycolide, polylactic acid, poly-3-hydroxybutyrate.

Assignments (2)
SECURITY INTEREST Recorded Sep 13, 2023
From: FLOW PHARMA, INC.
To: JOHN C. BRADY, TRUSTEE OF THE JCB TRUST DATED AUGUS 22, 2019
Reel/Frame 064894/0189 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 24, 2011
From: RUBSAMEN, REID M.; HECKERMAN, DAVID EARL
To: FLOW PHARMA, INC.
Reel/Frame 026798/0256 →
Continuity (4)
Provisional Application 61351672 · Jun 4, 2010
Provisional Application 61354632 · Jun 14, 2010
Provisional Application 61372413 · Aug 10, 2010
Related Publication 20110300226A1 · Dec 8, 2011