US2010111997A1PendingUtilityA1
Multi component vaccine containing clostridial and non-clostridial organisms in a low dose
Est. expiryMar 29, 2015(expired)· nominal 20-yr term from priority
A61P 33/02A61K 39/08A61K 39/102Y02A50/30
42
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Abstract
Disclosed herein is a multicomponent low dose vaccine comprising a safe and immunogenically effective combination of a protective antigen component or components of clostridial organism, a protective antigen component of a non-clostridial organism and an adjuvant.
Claims
exact text as granted — not AI-modified1 - 45 . (canceled)
46 . A method for reducing injection site lesion formation by at least 41% when immunizing cattle using an encapsulating polymer adjuvant in a multicomponent vaccine comprising an immunogenically effective combination of protective antigen components from at least six clostridial organisms, a protective antigen component from Moraxella Bovis ( M.Bovis ), and an encapsulating polymer adjuvant, comprising administering the multicomponent vaccine in a dose size of about 2 ml., thereby reducing injection site lesion formation by at least 41% compared with conventional injection of 5 ml of vaccine and accomplishing effective immunization.
47 . A method for reducing injection site lesion formation by at least 41% when immunizing cattle using an encapsulating polymer adjuvant in a multicomponent vaccine comprising an immunogenically effective combination of protective antigen components from seven clostridial organisms, a protective antigen component from M.Bovis, and an encapsulating polymer adjuvant, comprising administering the multicomponent vaccine in a dose size of about 2 ml., thereby reducing injection site lesion formation by at least 41% compared with conventional injection of 5 ml of said vaccine and accomplishing effective immunization.
48 . (canceled)
49 . The method of claim 46 , wherein the protective antigen components from clostridial organisms are selected from the group consisting of Cl. chauvoei, Cl. septicum, Cl novyi, Cl. perfringens type C, Cl. perfringens type D, Cl. sordellii, Cl. tetani and Cl. haemolyticum.
50 . The method of claim 46 , wherein each of the protective antigen components is adjuvanated separately, thereby encapsulating each component separately and causing each to be released slowly over a period of several weeks after administration.
51 . The method of claim 46 , wherein the multicomponent vaccine is administered intramuscularly.Cited by (0)
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