HRP20150790T1 - Režimi imunoterapije koji ovise o statusu apoe - Google Patents

Režimi imunoterapije koji ovise o statusu apoe Download PDF

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Publication number
HRP20150790T1
HRP20150790T1 HRP20150790TT HRP20150790T HRP20150790T1 HR P20150790 T1 HRP20150790 T1 HR P20150790T1 HR P20150790T T HRP20150790T T HR P20150790TT HR P20150790 T HRP20150790 T HR P20150790T HR P20150790 T1 HRP20150790 T1 HR P20150790T1
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Croatia
Prior art keywords
humanized antibody
antibody according
humanized
patient
seq
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HRP20150790TT
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English (en)
Inventor
Ronald Black
Lars Ekman
Ivan Lieberburg
Michael Grundman
James Callaway
Keith M. Gregg
Jack Steven Jacobsen
Davinder Gill
Lioudmila Tchistiakova
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Janssen Sciences Ireland Uc
Wyeth Llc
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Application filed by Janssen Sciences Ireland Uc, Wyeth Llc filed Critical Janssen Sciences Ireland Uc
Publication of HRP20150790T1 publication Critical patent/HRP20150790T1/hr

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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10Antioedematous agents; Diuretics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2896Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against molecules with a "CD"-designation, not provided for elsewhere
    • GPHYSICS
    • G06COMPUTING; CALCULATING OR COUNTING
    • G06QINFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
    • G06Q99/00Subject matter not provided for in other groups of this subclass
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/20Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/34Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/71Decreased effector function due to an Fc-modification
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C07K2317/732Antibody-dependent cellular cytotoxicity [ADCC]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C07K2317/734Complement-dependent cytotoxicity [CDC]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/77Internalization into the cell

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Business, Economics & Management (AREA)
  • Physics & Mathematics (AREA)
  • Theoretical Computer Science (AREA)
  • General Physics & Mathematics (AREA)
  • General Business, Economics & Management (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Psychiatry (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Peptides Or Proteins (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Claims (13)

1. Humanizirani oblik 3D6 antitijela koji sadrži humani konstantni dio teškog lanca sa mutacijama L234A, L235A i G237A, pri čemu su pozicije numerirane prema EU sustavu numeracije, naznačen time da 3D6 je antitijelo proizvedeno od ATCC pripojni broj PTA-5130.
2. Humanizirano antitijelo prema zahtjevu 1, naznačeno time da je izotip humani IgG1, IgG2 ili IgG4, poželjno IgG1.
3. Humanizirano antitijelo prema zahtjevu 1, naznačeno time da sadrži varijabilni dio lakog lanca sa zrelom sekvencom SEQ ID NO:2, i varijabilni dio teškog lanca sa zrelom sekvencom SEQ ID NO:3, pri čemu antitijelo ima humani IgG izotip.
4. Humanizirano antitijelo prema zahtjevu 1, naznačeno time da sadrži humanizirani laki lanac sa aminokiselinskom sekvencom koja sadrži SEQ ID NO:48 i humanizirani teški lanac sa aminokiselinskom sekvencom koja sadrži SEQ ID NO:66 ili 67.
5. Farmaceutski sastav, naznačen time da sadrži humanizirano antitijelo prema bilo kojem od zahtjeva 1-4.
6. Izolirana nukleinska kiselina koja kodira humanizirano antitijelo prema bilo kojem od zahtjeva 1-4, sa sekvencom koja sadrži SEQ ID NO:68, pod uvjetom da nukleotidi 1- 57 koji kodiraju signalnu sekvencu mogu a i ne moraju biti prisutni.
7. Humanizirano antitijelo prema bilo kojem od patentnih zahtjeva 1 do 4 za upotrebu u postupku liječenja ili obavljanja profilakse amiloidogene bolesti, naznačeno time da amiloidne naslage Aβ u mozgu kod pacijenta imaju nula ApoE4 alela.
8. Humanizirano antitijelo prema zahtjevu 7, naznačeno time da je za upotrebu prema zahtjevu 7, pri čemu se pacijentu koji ima nula ApoE4 alela daje doza od 0.5-2 mg/kg antitijela.
9. Humanizirano antitijelo prema bilo kojem od patentnih zahtjeva 1 do 4 za upotrebu u postupku liječenja ili obavljanja profilakse amiloidogene bolesti, naznačeno time da amiloidne naslage Aβ u mozgu, kod pacijenta imaju jedan ili dva ApoE4 alela.
10. Humanizirano antitijelo prema zahtjevu 9, za upotrebu prema zahtjevu 9, naznačeno time da se pacijentu koji ima jedan ili dva ApoE4 alela daje doza od 0.15-1 mg/kg antitijela.
11. Humanizirano antitijelo prema bilo kojem od patentnih zahtjeva 7 do 10 za upotrebu prema tim patentnim zahtjevima, naznačeno time da se kod pacijenta prati vazogeni edem, po mogućnosti pomoću MRI.
12. Humanizirano antitijelo prema bilo kojem od patentnih zahtjeva 7 do 11, za upotrebu prema tim patentnim zahtjevima, naznačeno time da je amiloidogena bolest koju karakteriziraju amiloidne naslage Aβ u mozgu Alzheimerova bolest.
13. Antitijelo prema bilo kojem od patentnih zahtjeva 1 do 4, za primjenu u liječenju ili profilaksi bolesti koju karakteriziraju amiloidne naslage u mozgu pacijenta, prema najmanje jednom od prvog i drugog režima, pri čemu se za izbor režima koristi određivanje broja kopija ApoE4.
HRP20150790TT 2007-10-17 2015-07-17 Režimi imunoterapije koji ovise o statusu apoe HRP20150790T1 (hr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US99942307P 2007-10-17 2007-10-17
US8382708P 2008-07-25 2008-07-25
PCT/US2008/080382 WO2009052439A2 (en) 2007-10-17 2008-10-17 Immunotherapy regimes dependent on apoe status
EP08839961.3A EP2207565B1 (en) 2007-10-17 2008-10-17 Immunotherapy regimes dependent on apoe status

Publications (1)

Publication Number Publication Date
HRP20150790T1 true HRP20150790T1 (hr) 2015-08-28

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Application Number Title Priority Date Filing Date
HRP20150790TT HRP20150790T1 (hr) 2007-10-17 2015-07-17 Režimi imunoterapije koji ovise o statusu apoe

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Country Link
US (3) US20090155256A1 (hr)
EP (2) EP2207565B1 (hr)
JP (2) JP5745853B2 (hr)
KR (1) KR101197839B1 (hr)
CN (2) CN101969988A (hr)
AR (1) AR071732A1 (hr)
AU (1) AU2008311823A1 (hr)
BR (1) BRPI0818000A2 (hr)
CA (2) CA2940337A1 (hr)
CL (1) CL2008003089A1 (hr)
CO (1) CO6331295A2 (hr)
CY (1) CY1116552T1 (hr)
DK (1) DK2207565T3 (hr)
EA (2) EA201590833A1 (hr)
ES (1) ES2547230T3 (hr)
HK (2) HK1146234A1 (hr)
HR (1) HRP20150790T1 (hr)
HU (1) HUE025684T2 (hr)
IL (1) IL205127A (hr)
JO (1) JO3076B1 (hr)
MX (1) MX2010004250A (hr)
MY (1) MY156454A (hr)
PA (1) PA8800801A1 (hr)
PE (1) PE20090971A1 (hr)
PL (1) PL2207565T3 (hr)
PT (1) PT2207565E (hr)
RS (1) RS54130B1 (hr)
SG (2) SG10201607589XA (hr)
SI (1) SI2207565T1 (hr)
TW (2) TW201206479A (hr)
WO (1) WO2009052439A2 (hr)
ZA (1) ZA201002544B (hr)

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