US2024042007A1PendingUtilityA1
Fluorocarbon-Linked Peptide Formulation
Est. expiryDec 31, 2030(~4.5 yrs left)· nominal 20-yr term from priority
A61K 39/00A61K 39/145A61K 39/385A61K 47/646A61K 39/12C12N 7/00A61K 2039/6093C12N 2760/16034C12N 2760/16134A61K 2039/60Y02A50/30A61K 2039/54A61K 2039/541A61K 2039/542A61K 2039/544C12N 2760/16122A61K 9/1075A61P 31/00A61P 31/04A61P 31/16A61P 35/00A61P 37/02A61P 37/04A61P 37/06A61K 47/12A61K 47/54
78
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The invention provides an aqueous acidic formulation suitable for use as in the preparation of a pharmaceutically acceptable fluorocarbon-linked peptide formulation, which aqueous formulation comprises a first fluorocarbon-linked peptide, wherein: the peptide linked to the fluorocarbon is at least 20 amino acid residues long, comprises at least 50% hydrophobic amino acid residues and has an isoelectric point greater than or equal to 7; and the fluorocarbon-linked peptide is present in micelles.
Claims
exact text as granted — not AI-modified1 - 27 . (canceled)
28 . A sterile, dried mixture of fluorocarbon-linked peptides, wherein the dried mixture comprises one or more fluorocarbon-linked peptides comprising 20 to 50 amino acid residues linked to a fluorocarbon, at least 50% hydrophobic amino acid residues, an isoelectric point greater than or equal to 7, and one or more T cell epitopes, not comprising a contiguous sequence of 20 amino acid residues comprising more than 80% hydrophobic amino acid residues; and wherein the mixture is in a solid form.
29 . The dried mixture of claim 28 , wherein the solid form is lyophilized as an amorphous cake or a powder.
30 . The dried mixture of claim 28 , wherein the solid form is dried by vacuum drying, spray-drying, freeze drying or fluid bed drying.
31 . The dried mixture of claim 28 , wherein the solid is freeze dried.
32 . The dried mixture of claim 28 , wherein the mixture is disposed in a vial, an ampoule or a syringe.
33 . The dried mixture of claim 32 , further comprising a pharmaceutically acceptable carrier.
34 . The dried mixture of claim 28 , wherein the peptide linked to the fluorocarbon is an immunogenic peptide having a sequence derived from (i) a protein or peptide from a pathogen or tumor cell or (ii) an autologous protein.
35 . The dried mixture of claim 28 , wherein the one or more T cell epitopes are from a pathogen, an autoimmune protein, or allergen or a tumor antigen.
36 . The dried mixture of claim 35 , wherein the pathogen is a virus, bacterium, mycobacterium, parasite or fungus.
37 . The dried mixture according to claim 28 , wherein the fluorocarbon comprises a chain from 3 to 20 carbon atoms, wherein one or more fluorine moieties is optionally replaced with a halogen moiety of Cl, Br, or I; a methyl group; or a hydrogen.
38 . The dried mixture according to claim 28 , wherein the fluorocarbon comprises the formula C 8 F 17 (CH 2 ) 2 .
39 . The dried mixture according to claim 28 , wherein the one or more fluorocarbon-linked peptides are present in micelles.
40 . A sterile, dried mixture of fluorocarbon-linked immunogenic peptides, wherein the dried mixture comprises one or more fluorocarbon-linked immunogenic peptides comprising 20 to 50 amino acid residues linked to a fluorocarbon, at least 50% hydrophobic amino acid residues, an isoelectric point greater than or equal to 7, and one or more T cell epitopes, not comprising a contiguous sequence of 20 amino acid residues comprising more than 80% hydrophobic amino acid residues;
wherein the immunogenic peptides are derived from Hepatitis B virus (HBV); and, wherein the mixture is in a solid form.
41 . The dried mixture of claim 40 , wherein the solid form is lyophilized as an amorphous cake or a powder.
42 . The dried mixture of claim 40 , wherein the solid form is dried by vacuum drying, spray-drying, freeze drying or fluid bed drying.
43 . The dried mixture of claim 40 , wherein the solid is freeze dried.
44 . The dried mixture of claim 40 , wherein the mixture is disposed in a vial, an ampoule or a syringe.
45 . The dried mixture of claim 44 , further comprising a pharmaceutically acceptable carrier.
46 . The dried mixture according to claim 40 , wherein the fluorocarbon comprises a chain from 3 to 20 carbon atoms, wherein one or more fluorine moieties is optionally replaced with a halogen moiety of Cl, Br, or I; a methyl group; or a hydrogen.
47 . The dried mixture according to claim 40 , wherein the fluorocarbon comprises the formula C 8 F 17 (CH 2 ) 2 .Join the waitlist — get patent alerts
Track US2024042007A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.