HRP20180302T1 - Stable and soluble antibodies - Google Patents

Stable and soluble antibodies Download PDF

Info

Publication number
HRP20180302T1
HRP20180302T1 HRP20180302TT HRP20180302T HRP20180302T1 HR P20180302 T1 HRP20180302 T1 HR P20180302T1 HR P20180302T T HRP20180302T T HR P20180302TT HR P20180302 T HRP20180302 T HR P20180302T HR P20180302 T1 HRP20180302 T1 HR P20180302T1
Authority
HR
Croatia
Prior art keywords
antibody
pharmaceutical preparation
seq
sequence
tnfα
Prior art date
Application number
HRP20180302TT
Other languages
Croatian (hr)
Inventor
Leonardo Borras
David Urech
Original Assignee
Esbatech - A Novartis Company Llc
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
Priority claimed from PCT/CH2011/000256 external-priority patent/WO2012051734A1/en
Application filed by Esbatech - A Novartis Company Llc filed Critical Esbatech - A Novartis Company Llc
Publication of HRP20180302T1 publication Critical patent/HRP20180302T1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/24Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons

Claims (14)

1. Protutijelo koje se specifično veže na ljudski TNFα, naznačeno time, da obuhvaća sljedeće: a) varijabilni laki lanac koji sadrži sekvencu od SEQ ID NO: 2 ili SEQ ID NO: 14; i b) varijabilni teški lanac koji sadrži sekvencu od SEQ ID NO: 5.1. An antibody that specifically binds to human TNFα, characterized in that it comprises the following: a) variable light chain containing the sequence of SEQ ID NO: 2 or SEQ ID NO: 14; and b) a variable heavy chain containing the sequence of SEQ ID NO: 5. 2. Protutijelo prema zahtjevu 1, naznačeno time, da sadrži poveznicu koja obuhvaća sekvencu od SEQ ID NO: 7.2. The antibody according to claim 1, characterized in that it contains a linker comprising the sequence of SEQ ID NO: 7. 3. Protutijelo prema zahtjevu 1, naznačeno time, da protutijelo obuhvaća sekvencu od SEQ ID NO: 10 ili SEQ ID NO: 17.3. The antibody according to claim 1, characterized in that the antibody comprises the sequence of SEQ ID NO: 10 or SEQ ID NO: 17. 4. Farmaceutski pripravak, naznačen time, da obuhvaća terapeutski učinkovitu količinu protutijela prema bilo kojem od zahtjeva 1 do 3 i farmaceutski prihvatljiv nosač.4. A pharmaceutical preparation, characterized in that it comprises a therapeutically effective amount of the antibody according to any one of claims 1 to 3 and a pharmaceutically acceptable carrier. 5. Farmaceutski pripravak prema zahtjevu 4, naznačen time, da se upotrebljava za liječenje bolesti posredovane putem TNFα.5. Pharmaceutical preparation according to claim 4, characterized in that it is used for the treatment of a disease mediated by TNFα. 6. Farmaceutski pripravak prema zahtjevu 4, za uporabu prema zahtjevu 5, naznačen time, da se kod bolesti koja je posredovana putem TNFα, radi o očnom poremećaju odabranom iz skupine koju čine: uveitis, Bechetova bolest, retinitis, suho oko, glaukom, Sjögrenov sindrom, dijabetska neuropatija, skleritis, makularna degeneracija povezana sa starosnom dobi i keratitis.6. Pharmaceutical preparation according to claim 4, for use according to claim 5, characterized in that the disease mediated by TNFα is an eye disorder selected from the group consisting of: uveitis, Bechet's disease, retinitis, dry eye, glaucoma, Sjögren's syndrome, diabetic neuropathy, scleritis, age-related macular degeneration and keratitis. 7. Farmaceutski pripravak prema zahtjevu 4, za uporabu prema zahtjevu 5, naznačen time, da se farmaceutski pripravak treba davati putem sljedećih primjena: okularna, intranazalna, otička, sublingvalna, transdermalna, topikalna, oralna, nazalna, rektalna ili parenteralna.7. Pharmaceutical preparation according to claim 4, for use according to claim 5, characterized in that the pharmaceutical preparation should be administered through the following applications: ocular, intranasal, otic, sublingual, transdermal, topical, oral, nasal, rectal or parenteral. 8. Farmaceutski pripravak prema zahtjevu 7, za uporabu prema zahtjevu 7, naznačen time, da se farmaceutski pripravak treba davati u jednostrukoj ili podijeljenoj dozi koja sadrži od 0,1 do 100 mg protutijela.8. Pharmaceutical preparation according to claim 7, for use according to claim 7, characterized in that the pharmaceutical preparation should be administered in a single or divided dose containing from 0.1 to 100 mg of antibody. 9. Farmaceutski pripravak prema zahtjevu 7, za uporabu prema zahtjevu 7, naznačen time, da se kod bolesti koja je posredovana putem TNFα, radi o uveitisu, a farmaceutski pripravak se primjenjuje topikalno u oko pojedinca.9. Pharmaceutical preparation according to claim 7, for use according to claim 7, characterized in that the disease mediated by TNFα is uveitis, and the pharmaceutical preparation is applied topically to the individual's eye. 10. Izolirana molekula nukleinske kiseline, naznačena time, da ona kodira protutijelo prema zahtjevu 1.10. An isolated nucleic acid molecule, characterized in that it encodes an antibody according to claim 1. 11. Vektor, naznačen time, da on obuhvaća molekulu nukleinske kiseline prema zahtjevu 10.11. Vector, characterized in that it comprises a nucleic acid molecule according to claim 10. 12. Stanica domaćina, naznačena time, da ona obuhvaća vektor prema zahtjevu 11.12. The host cell, characterized in that it comprises the vector according to claim 11. 13. Protutijelo prema zahtjevu 1, naznačeno time, da protutijelo je Fab, Fab’, F(ab)’2, Fv jednostrukog lanca (scFv), Fv fragment, ili linearno protutijelo.13. Antibody according to claim 1, characterized in that the antibody is Fab, Fab', F(ab)'2, Fv single chain (scFv), Fv fragment, or linear antibody. 14. Bivalentna ili bispecifična molekula, naznačena time, da ona obuhvaća protutijelo prema zahtjevu 1.14. Bivalent or bispecific molecule, characterized in that it comprises an antibody according to claim 1.
HRP20180302TT 2010-10-22 2018-02-20 Stable and soluble antibodies HRP20180302T1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US40579810P 2010-10-22 2010-10-22
US201161405798P 2011-05-11 2011-05-11
PCT/CH2011/000256 WO2012051734A1 (en) 2010-10-22 2011-10-24 Stable and soluble antibodies
EP11776322.7A EP2630159B1 (en) 2010-10-22 2011-10-24 Stable and soluble antibodies

Publications (1)

Publication Number Publication Date
HRP20180302T1 true HRP20180302T1 (en) 2018-05-04

Family

ID=45637301

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20180302TT HRP20180302T1 (en) 2010-10-22 2018-02-20 Stable and soluble antibodies

Country Status (6)

Country Link
DK (1) DK2630159T3 (en)
ES (2) ES2848556T3 (en)
HR (1) HRP20180302T1 (en)
HU (1) HUE036125T2 (en)
LT (1) LT2630159T (en)
PT (1) PT2630159T (en)

Also Published As

Publication number Publication date
LT2630159T (en) 2018-03-12
ES2660613T3 (en) 2018-03-23
HUE036125T2 (en) 2018-06-28
ES2848556T3 (en) 2021-08-10
DK2630159T3 (en) 2018-02-26
PT2630159T (en) 2018-02-28

Similar Documents

Publication Publication Date Title
JP2013544078A5 (en)
RU2016122041A (en) NEW ANTI-CLAUDIN ANTIBODIES AND WAYS OF THEIR APPLICATION
RU2015100231A (en) METHOD FOR SELECTING AND OBTAINING SELECTIVE AND MULTI-SPECIFIC THERAPEUTIC MOLECULES WITH SPECIFIED PROPERTIES, INCLUDING AT LEAST TWO DIFFERENT TARGETING GROUPS, AND THEIR APPLICATIONS
JP2013522237A5 (en)
HRP20200070T1 (en) Human antibodies that bind lymphocyte activation gene-r (lag-3) and uses thereof
JP2013517277A5 (en)
JP2017530722A5 (en)
JP2017512193A5 (en)
JP2015535828A5 (en)
JP2013529183A5 (en)
JP2017514461A5 (en)
HRP20151257T1 (en) Monoclonal antibodies against claudin-18 for treatment of cancer
JP2011501671A5 (en)
JP2016116536A5 (en)
HRP20191129T1 (en) Anti-clusterin antibodies and antigen binding fragments and their use to reduce tumor volume
JP2010507594A5 (en)
RU2014120629A (en) ANTIGEN-BINDING PROTEIN AND ITS APPLICATION AS A PRODUCT FOR ADDRESSED DELIVERY IN TREATMENT OF CANCER
JP2018536632A5 (en) Molecules that specifically bind to B7-H3 and molecules that specifically bind to PD-1
JP2015534580A5 (en)
JP2014534239A5 (en)
JP2020502271A5 (en)
UA113728C2 (en) PHARMACEUTICAL COMPOSITION CONTAINING ANTIBODY TO AN PCSK9 HUMAN
JP2017506669A5 (en) Composition for use in the treatment of glioblastoma and use thereof
RU2016129894A (en) COVALENTLY RELATED HELICAR-ANTIBODY CONJUGATES AGAINST HELICAR AND THEIR APPLICATION
JP2014502955A5 (en)