US2008171079A1PendingUtilityA1
Vaccine
Est. expiryMar 3, 2025(expired)· nominal 20-yr term from priority
A61P 37/04A61P 29/00A61P 25/04A61P 31/18A61P 31/22A61P 25/00A61P 31/00C12N 2710/16722A61K 39/12C07K 14/005A61K 2039/55555C12N 2710/16734A61K 2039/5252A61K 39/25A61K 2039/5254A61K 2039/55577A61K 2039/55572A61K 39/00A61K 39/39
52
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Use of an immunogenic composition comprising VZV gE, or immunogenic fragment thereof, and a TH-1 adjuvant in the preparation of a medicament for the prevention or amelioration of shingles and/or post herpetic neuralgia. Compositions comprising a truncated VZV gE antigen and an adjuvant containing QS21, cholesterol and 3D MPL are also claimed
Claims
exact text as granted — not AI-modified1 . A method of preventing or ameliorating shingles and/or post herpetic neuralgia in a patient in need thereof, said method comprising the step of administering to said patient an effective amount of an immunogenic composition comprising VZV gE, or immunogenic fragment thereof, and a TH-1 adjuvant.
2 . The method according to claim 1 wherein the adjuvant comprises QS21.
3 . The method according to claim 1 , wherein the adjuvant comprises liposomes.
4 . The method according to claim 3 , wherein the liposomes comprise cholesterol.
5 . The method according to claim 1 , wherein the adjuvant comprises 3D MPL.
6 . The method according to claim 5 , wherein the MPL is comprised within a liposome.
7 . The method according to claim 1 , wherein the gE is a truncate. Currently
8 . The method according to claim 7 , wherein the gE is a C-terminal truncate.
9 . The method according to claim 8 , wherein the gE has the amino acid sequence of SEQ ID NO: 1.
10 . The method according to claim 1 , wherein the immunogenic composition is administered to a population of individuals older than 50.
11 . The method according to claim 1 , wherein the immunogenic composition is administered to a population of immunocompromised individuals.
12 . A method for preventing and/or decreasing the severity of herpes zoster and/or post herpetic neuralgia, the method comprising delivery to an individual in need thereof an effective amount of a composition comprising VZV gE, or immunogenic fragment thereof, and a TH-1 adjuvant.
13 . An immunogenic composition or vaccine consisting essentially of a VZV gE antigen truncated to remove the carboxy terminal anchor region in combination with an adjuvant comprising QS21, 3D MPL, and liposomes comprising cholesterol.
14 . The method according to claim 12 , wherein the method further comprises sequential or concomitant delivery to an individual of a VZV antigen or immunogenic derivative thereof and a live attenuated VZV or whole inactivated VZV.
15 . (canceled)
16 . The method according to claim 14 , wherein a VZV antigen is delivered concomitantly with live attenuated VZV.
17 . The method or use according to claim 14 , wherein the VZV antigen is a C-terminally truncated gE antigen and wherein the live attenuated VZV is an attenuated VZV OKA strain.
18 . A kit comprising a live attenuated VZV or whole inactivated VZV and, separately, a VZV antigen or immunogenic derivative thereof, the components suitable for concomitant or sequential delivery, or for mixing as a single composition prior to delivery.
19 . A kit comprising as separate components, a TH-1 adjuvant and a gE antigen or immunogenic fragment thereof, suitable for extemporaneous preparation of a vaccine composition for the prevention or amelioration of shingles and/or post herpetic neuralgia.Join the waitlist — get patent alerts
Track US2008171079A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.