AR118780A1 - THERAPEUTICS OF FULLY HUMAN POST-TRANSLATIONALLY MODIFIED ANTIBODIES - Google Patents

THERAPEUTICS OF FULLY HUMAN POST-TRANSLATIONALLY MODIFIED ANTIBODIES

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Publication number
AR118780A1
AR118780A1 ARP200101169A ARP200101169A AR118780A1 AR 118780 A1 AR118780 A1 AR 118780A1 AR P200101169 A ARP200101169 A AR P200101169A AR P200101169 A ARP200101169 A AR P200101169A AR 118780 A1 AR118780 A1 AR 118780A1
Authority
AR
Argentina
Prior art keywords
fully human
translationally modified
methods
post
therapeutics
Prior art date
Application number
ARP200101169A
Other languages
Spanish (es)
Inventor
Justin Glenn
Xu Wang
Devin Mdougald
Chunping Qiao
Joseph Bruder
Franz Gerner
Everen Sherri Van
Ye Liu
Zuchun Wu
Olivier Danos
Original Assignee
Regenxbio Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Regenxbio Inc filed Critical Regenxbio Inc
Publication of AR118780A1 publication Critical patent/AR118780A1/en

Links

Abstract

Se proporcionan métodos y composiciones para la administración de anticuerpos monoclonales terapéuticos postraduccionalmente modificados, completamente humanos y los fragmentos de unión a antígeno de los mismos. Los anticuerpos monoclonales terapéuticos postraduccionalmente modificados, completamente humanos pueden administrarse mediante métodos de terapia génica, por ejemplo, como un vector de virus recombinante adenoasociado (rAAV) al tejido apropiado. También se proporcionan métodos de preparación de los vectores AAV, composiciones farmacéuticas y métodos de tratamiento. Además, se proporcionan métodos para producir anticuerpos terapéuticos que están “biomejorados” como completamente humanos, postraduccionalmente modificados. Estos anticuerpos terapéuticos postraduccionalmente modificados, completamente humanos pueden administrarse a un sujeto que necesita tratamiento con el anticuerpo terapéutico.Methods and compositions are provided for the administration of fully human post-translationally modified therapeutic monoclonal antibodies and antigen-binding fragments thereof. The fully human, post-translationally modified therapeutic monoclonal antibodies can be delivered by gene therapy methods, for example, as a recombinant adeno-associated virus (rAAV) vector to the appropriate tissue. Also provided are methods of preparing the AAV vectors, pharmaceutical compositions, and methods of treatment. In addition, methods are provided for producing therapeutic antibodies that are post-translationally modified as fully human "bi-enhanced". These fully human, post-translationally modified therapeutic antibodies can be administered to a subject in need of treatment with the therapeutic antibody.

ARP200101169A 2019-04-24 2020-04-24 THERAPEUTICS OF FULLY HUMAN POST-TRANSLATIONALLY MODIFIED ANTIBODIES AR118780A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201962838165P 2019-04-24 2019-04-24

Publications (1)

Publication Number Publication Date
AR118780A1 true AR118780A1 (en) 2021-10-27

Family

ID=78803872

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP200101169A AR118780A1 (en) 2019-04-24 2020-04-24 THERAPEUTICS OF FULLY HUMAN POST-TRANSLATIONALLY MODIFIED ANTIBODIES

Country Status (1)

Country Link
AR (1) AR118780A1 (en)

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