Curevac’s patent involves an mRNA sequence for RSV infections, focusing on a pharmaceutical composition with a modified RSV-F protein. The composition aims to develop a vaccine for prophylaxis or treatment of RSV infections, utilizing a specific mRNA molecule formulation. GlobalData’s report on Curevac gives a 360-degree view of the company including its patenting strategy. Buy the report here.
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According to GlobalData’s company profile on Curevac, Personalized cancer vaccines was a key innovation area identified from patents. Curevac's grant share as of April 2024 was 38%. Grant share is based on the ratio of number of grants to total number of patents.
Pharmaceutical composition for rsv vaccine with modified fusion protein
A recently granted patent (Publication Number: US11965000B2) discloses a pharmaceutical composition comprising a mRNA molecule encoding a Respiratory Syncytial Virus fusion protein (RSV-F) with a deleted C-terminus (F-del), lacking specific amino acids. The mRNA molecule is formulated with a cationic lipid and includes a 5'-cap structure, 5' and 3' untranslated regions, a poly(A) sequence, and a stabilizing sequence from the alpha globin 3' UTR. Additionally, the composition may include a second mRNA encoding an antigen from a different virus. The pharmaceutical composition is designed for intramuscular injection and aims to stimulate an immune response to RSV by producing RSV neutralizing antibodies.
Furthermore, the patent also covers a method for stimulating an immune response to RSV in a subject by administering the pharmaceutical composition described above. The method involves intradermal or intramuscular injection of the composition, which includes a cationic component and a poly(A) sequence of specific length. By utilizing this method, an increased amount of RSV neutralizing antibodies can be generated compared to compositions encoding full-length RSV-F. The method emphasizes the importance of the specific mRNA structure, including the 5' cap structure, 3' UTR stabilizing sequence, and the inclusion of a transmembrane domain of native RSV-F, in enhancing the immune response against RSV.
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