AR123085A1 - ANTI-INTEGRIN b7 ANTIBODY FORMULATIONS AND DEVICES - Google Patents

ANTI-INTEGRIN b7 ANTIBODY FORMULATIONS AND DEVICES

Info

Publication number
AR123085A1
AR123085A1 ARP210102115A ARP210102115A AR123085A1 AR 123085 A1 AR123085 A1 AR 123085A1 AR P210102115 A ARP210102115 A AR P210102115A AR P210102115 A ARP210102115 A AR P210102115A AR 123085 A1 AR123085 A1 AR 123085A1
Authority
AR
Argentina
Prior art keywords
hvr
seq
integrin
amino acid
acid sequence
Prior art date
Application number
ARP210102115A
Other languages
Spanish (es)
Inventor
Jennifer Pulley
Meina Tao Tang
Swati Tole
Helen Tyrrell
Mariam Abousossein
Hemanth Amarchinta
Audrey Boruvka
Han Ting Ding
Heather L Flores
Glen Scott Giese
Renato Ravanello
Wenhui Zhang
Original Assignee
Genentech Inc
Hoffmann La Roche
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 Genentech Inc, Hoffmann La Roche filed Critical Genentech Inc
Publication of AR123085A1 publication Critical patent/AR123085A1/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
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2839Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the integrin superfamily
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39591Stabilisation, fragmentation
    • 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
    • C07K2317/90Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/94Stability, e.g. half-life, pH, temperature or enzyme-resistance

Abstract

Se proporcionan formulaciones que comprenden un anticuerpo anti-integrina b7 o un fragmento de unión a antígeno del mismo, que incluyen formulaciones farmacéuticas. También se proporcionan artículos de fabricación que comprenden dichas formulaciones y métodos para usar dichas formulaciones. Reivindicación 1: Una formulación que comprende un anticuerpo monoclonal anti-integrina b7, en la que la concentración del anticuerpo anti-integrina b7 es al menos aproximadamente 100 mg/ml, la viscosidad de la formulación es menor que aproximadamente 20 centipoises (cP) a 25ºC y en la que la formulación tiene estabilidad extendida. Reivindicación 30: Una formulación que comprende un anticuerpo anti-integrina b7, en tampón histidina 20 mM o en tampón histidina aproximadamente 20 mM, pH 5,8 o pH entre 5,7 y 5,9 o pH entre 5,75 y 5,85, polisorbato 20 al 0,04% o polisorbato 20 aproximadamente al 0,04% y succinato de arginina 200 mM o succinato de arginina aproximadamente 200 mM, en la que la concentración del anticuerpo anti-integrina b7 es 150 mg/ml o aproximadamente 150 mg/ml, y en la que el anticuerpo anti-integrina b7 comprende tres regiones hipervariables (HVR) de la cadena ligera, HVR-L1, HVR-L2 y HVR-L3, y tres HVR de la cadena pesada, HVR-H1, HVR-H2 y HVR-H3, en las que: (i) la HVR-L1 comprende la secuencia de aminoácidos expuesta en SEQ ID Nº 1; (ii) la HVR-L2 comprende la secuencia de aminoácidos expuesta en SEQ ID Nº 2; (iii) la HVR-L3 comprende la secuencia de aminoácidos expuesta en SEQ ID Nº 3; (iv) la HVR-H1 comprende la secuencia de aminoácidos expuesta en SEQ ID Nº 4; (v) la HVR-H2 comprende la secuencia de aminoácidos SEQ ID Nº 5; y (vi) la HVR-H3 comprende la secuencia de aminoácidos expuesta en SEQ ID Nº 6 o SEQ ID Nº 7.Formulations comprising an anti-β7 integrin antibody or an antigen-binding fragment thereof are provided, including pharmaceutical formulations. Articles of manufacture comprising said formulations and methods of using said formulations are also provided. Claim 1: A formulation comprising an anti-β7 integrin monoclonal antibody, wherein the concentration of the anti-β7 integrin antibody is at least about 100 mg/mL, the viscosity of the formulation is less than about 20 centipoise (cP) at 25°C and wherein the formulation has extended stability. Claim 30: A formulation comprising an anti-integrin b7 antibody, in 20 mM histidine buffer or in approximately 20 mM histidine buffer, pH 5.8 or pH between 5.7 and 5.9 or pH between 5.75 and 5, 85, 0.04% polysorbate 20 or about 0.04% polysorbate 20 and 200 mM arginine succinate or about 200 mM arginine succinate, wherein the concentration of the anti-integrin b7 antibody is 150 mg/ml or about 150 mg/ml, and wherein the anti-β7 integrin antibody comprises three light chain hypervariable regions (HVRs), HVR-L1, HVR-L2, and HVR-L3, and three heavy chain HVRs, HVR-H1 , HVR-H2 and HVR-H3, wherein: (i) the HVR-L1 comprises the amino acid sequence set forth in SEQ ID NO: 1; (ii) the HVR-L2 comprises the amino acid sequence set forth in SEQ ID NO: 2; (iii) the HVR-L3 comprises the amino acid sequence set forth in SEQ ID NO: 3; (iv) HVR-H1 comprises the amino acid sequence set forth in SEQ ID NO: 4; (v) the HVR-H2 comprises the amino acid sequence SEQ ID NO: 5; and (vi) the HVR-H3 comprises the amino acid sequence set forth in SEQ ID No. 6 or SEQ ID No. 7.

ARP210102115A 2020-07-31 2021-07-29 ANTI-INTEGRIN b7 ANTIBODY FORMULATIONS AND DEVICES AR123085A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US202063059427P 2020-07-31 2020-07-31

Publications (1)

Publication Number Publication Date
AR123085A1 true AR123085A1 (en) 2022-10-26

Family

ID=77693570

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP210102115A AR123085A1 (en) 2020-07-31 2021-07-29 ANTI-INTEGRIN b7 ANTIBODY FORMULATIONS AND DEVICES

Country Status (11)

Country Link
EP (1) EP4188958A1 (en)
JP (1) JP2023536158A (en)
KR (1) KR20230041071A (en)
AR (1) AR123085A1 (en)
AU (1) AU2021316017A1 (en)
BR (1) BR112023001734A2 (en)
CA (1) CA3190109A1 (en)
IL (1) IL300133A (en)
MX (1) MX2023001157A (en)
TW (1) TW202222832A (en)
WO (1) WO2022026699A1 (en)

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US6040498A (en) 1998-08-11 2000-03-21 North Caroline State University Genetically engineered duckweed
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US20050158303A1 (en) 2003-04-04 2005-07-21 Genentech, Inc. Methods of treating IgE-mediated disorders comprising the administration of high concentration anti-IgE antibody formulations
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Also Published As

Publication number Publication date
WO2022026699A1 (en) 2022-02-03
CA3190109A1 (en) 2022-02-03
IL300133A (en) 2023-03-01
TW202222832A (en) 2022-06-16
AU2021316017A1 (en) 2023-02-16
BR112023001734A2 (en) 2023-02-28
EP4188958A1 (en) 2023-06-07
KR20230041071A (en) 2023-03-23
JP2023536158A (en) 2023-08-23
MX2023001157A (en) 2023-02-22

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