Claims for Patent: 10,682,426
✉ Email this page to a colleague
Summary for Patent: 10,682,426
Title: | Rabies vaccine |
Abstract: | The present invention relates to an mRNA sequence, comprising a coding region, encoding at least one antigenic peptide or protein of Rabies virus or a fragment, variant or derivative thereof. Additionally the present invention relates to a composition comprising a plurality of mRNA sequences comprising a coding region, encoding at least one antigenic peptide or protein of Rabies virus or a fragment, variant or derivative thereof. Furthermore it also discloses the use of the mRNA sequence or the composition comprising a plurality of mRNA sequences for the preparation of a pharmaceutical composition, especially a vaccine, e.g. for use in the prophylaxis or treatment of Rabies virus infections. The present invention further describes a method of treatment or prophylaxis of rabies using the mRNA sequence. |
Inventor(s): | Schnee; Margit (Constance, DE), Kramps; Thomas (Tubingen, DE), Stitz; Lothar (Rottenburg, DE), Petsch; Benjamin (Tubingen, DE) |
Assignee: | CureVac AG (Tubingen, DE) |
Application Number: | 15/048,356 |
Patent Claims: | 1. A method of treatment or prophylaxis of rabies virus infections comprising the steps: a) providing an mRNA having a sequence comprising a coding region encoding
glycoprotein G (RAV-G) of Rabies virus, wherein the G/C content of the coding region is increased compared with the G/C content of the coding region of the wild type mRNA, and wherein the coded amino acid sequence of said GC-enriched mRNA is not being
modified compared with the coded amino acid sequence of the wild type mRNA, and wherein: (i) the mRNA comprises a sequence at least 95% identical to SEQ ID No: 24; or (ii) wherein the mRNA further comprises a 5'-UTR element which comprises a nucleic
acid sequence which is derived from the 5'UTR of a TOP gene; b) applying or administering the mRNA to a tissue or an organism; c) optionally administering rabies immune globulin.
2. The method of claim 1, wherein the coding region encodes the full-length protein of glycoprotein G (RAV-G) of Rabies virus. 3. The method of claim 1, wherein the glycoprotein G (RAV-G) is from a Rabies vaccine strain. 4. The method of claim 1, wherein the mRNA further comprises a) a 5'-CAP structure, b) a poly(A) sequence, c) and optionally a poly (C) sequence. 5. The method of claim 4, wherein the poly(A) sequence comprises a sequence of about 25 to about 400 adenosine nucleotides. 6. The method of claim 1, wherein the mRNA further comprises at least one histone stem-loop. 7. The method of claim 1, wherein the mRNA further comprises a 3'-UTR element. 8. The method of claim 7, wherein the 3'UTR element comprises a nucleic acid sequence which is derived from a 3'UTR of a gene providing a stable mRNA or from a homolog. 9. The method of claim 8, wherein the 3'UTR element comprises a nucleic acid sequence derived from a 3'UTR of a gene selected from the group consisting of an albumin gene, an .alpha.-globin gene, a .beta.-globin gene, a tyrosine hydroxylase gene, a lipoxygenase gene, and a collagen alpha gene. 10. The method of claim 9, wherein the 3'-UTR element comprises a nucleic acid sequence derived from a 3'UTR of .alpha.-globin gene. 11. The method of claim 7, wherein the at least one 3'UTR element comprises a nucleic acid sequence which is derived from the 3'UTR of a vertebrate albumin gene. 12. The method of claim 11, wherein the 3'UTR element is derived from a nucleic acid sequence according to SEQ ID NO. 18. 13. The method of claim 1, wherein the mRNA comprises, in 5'- to 3'-direction: a) a 5'-CAP structure; b) a coding region encoding at least one of glycoprotein G (RAV-G) of Rabies virus; c) a 3'-UTR element comprising or consisting of a nucleic acid sequence which is derived from an alpha globin gene or an albumin gene; d) a poly(A) sequence; e) a poly(C) sequence; and f) a histone-stem-loop. 14. The method of claim 13, wherein the mRNA comprises the RNA sequence of SEQ ID No. 24. 15. The method of claim 1, wherein the mRNA further comprises a 5'-UTR element which comprises a nucleic acid sequence which is derived from the 5'UTR of a TOP gene. 16. The method of claim 15, wherein the 5'UTR element comprises a nucleic acid sequence which is derived from a 5'UTR of a TOP gene encoding a ribosomal protein. 17. The method of claim 16, wherein the 5'UTR element comprises a nucleic acid sequence which is derived from a 5'UTR of a TOP gene encoding a ribosomal Large protein (RPL). |
Details for Patent 10,682,426
Applicant | Tradename | Biologic Ingredient | Dosage Form | BLA | Approval Date | Patent No. | Expiredate |
---|---|---|---|---|---|---|---|
Bavarian Nordic A/s | RABAVERT | rabies vaccine | For Injection | 103334 | October 20, 1997 | 10,682,426 | 2033-08-21 |
Sanofi Pasteur Sa | IMOVAX RABIES | rabies vaccine | For Injection | 103931 | February 04, 2000 | 10,682,426 | 2033-08-21 |
Octapharma Pharmazeutika Produktionsges.m.b.h. | OCTAGAM | immune globulin intravenous (human) | Injection | 125062 | May 21, 2004 | 10,682,426 | 2033-08-21 |
Octapharma Pharmazeutika Produktionsges.m.b.h. | OCTAGAM | immune globulin intravenous (human) | Injection | 125062 | March 26, 2007 | 10,682,426 | 2033-08-21 |
Octapharma Pharmazeutika Produktionsges.m.b.h. | OCTAGAM | immune globulin intravenous (human) | Injection | 125062 | July 11, 2014 | 10,682,426 | 2033-08-21 |
>Applicant | >Tradename | >Biologic Ingredient | >Dosage Form | >BLA | >Approval Date | >Patent No. | >Expiredate |
Make Better Decisions: Try a trial or see plans & pricing
Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.