DK2696888T3 - Sammensætninger og fremgangsmåder til forebyggelse eller behandling af pulmonal fibrose - Google Patents

Sammensætninger og fremgangsmåder til forebyggelse eller behandling af pulmonal fibrose Download PDF

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Publication number
DK2696888T3
DK2696888T3 DK12771584.5T DK12771584T DK2696888T3 DK 2696888 T3 DK2696888 T3 DK 2696888T3 DK 12771584 T DK12771584 T DK 12771584T DK 2696888 T3 DK2696888 T3 DK 2696888T3
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kinase
pharmaceutical composition
another embodiment
therapeutic
lung
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DK12771584.5T
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English (en)
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Cynthia Lander
Colleen Brophy
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Moerae Matrix Inc
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/10Peptides having 12 to 20 amino acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/19Cytokines; Lymphokines; Interferons
    • A61K38/21Interferons [IFN]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/39Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin, cold insoluble globulin [CIG]
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system

Claims (8)

1. Farmaceutisk sammensætning til anvendelse ved behandling af pulmonal fibrose i et individ, der er et resultat af administration af bleomycin, en allergisk reaktion, inhalation af miljøpartikler, rygning, en bakteriel infektion, en viral infektion, mekanisk beskadigelse på en lunge af individet, afvisning af en lungetransplantation, en autoimmun lidelse, en genetisk lidelse eller en kombination deraf, hvilken pulmonal fibrose er kendetegnet ved mindst en patologi udvalgt fra gruppen, der består af en afvigende afsætning af et ekstracellulært matrix-protein i et pulmonalt interstitium, en afvigende fremme af fibroblastproliferation i lungen, en afvigende induktion af myofibroblastdifferentiering i lungen og en afvigende fremme af fastgørelse af myofibroblaster til en ekstracellulær matrix, sammenlignet med et normalt sundt kontrol individ, hvilken farmaceutiske sammensætning omfatter (a) en terapeutisk mængde af et polypeptid af aminosyresekvensen YARAAARQARAKALARQLGVAA (SEQ ID NO: 1) eller en funktionel ækvivalent deraf, som er valgt fra gruppen, der består af et polypeptid af aminosyresekvensen FAKLAARLYRKALARQLGVAA (SEQ ID NO: 3); et polypeptid af aminosyresekvensen KAFAKLAARLYRKALAR-QLGVAA (SEQ ID NO: 4); og et polypeptid af aminosyresekvens HRRIKAWLKKIKALARQLGVAA (SEQ ID NO: 7); og (b) en farmaceutisk acceptabel bærer, hvor den terapeutiske mængde er effektiv (1) til at inhibere kinaseaktivitet af en kinase, som er valgt fra gruppen af en mitogen-aktiveret proteinkinase-aktiveret proteinkinase 2 (MK2), en mitogen-aktiveret proteinkinase-aktiveret proteinkinase 3 (MK3), en calcium/calmodulin-afhængig proteinkinase I (CaMKI, serin/threonin-specifik proteinkinase) og en BDNF/NT-3 vækstfaktorreceptor (TrkB, ty-rosinkinase); og (2) til at reducere fibroblastproliferation og ekstracellulær matrixaflejring i individets væv.
2. Farmaceutisk sammensætning til anvendelsen ifølge krav 1, hvor (a) den pulmonale fibrose er yderligere kendetegnet ved en betændelse i lungevævet; eller (b) den afvigende fibroblastproliferation og ekstracellulære matrixaflejring i vævet er kendetegnet ved en afvigende aktivitet af mitogen-aktiveret proteinkina-se-aktiveret proteinkinase 2 (MK2) i vævet sammenlignet med aktiviteten af mi-togen-aktiveret proteinkinase-aktiveret proteinkinase 2 (MK2) i vævet af et normalt sundt kontrolindivid.
3. Farmaceutisk sammensætning til anvendelse ifølge krav 2, hvor inflammationen er medieret af mindst et cytokin, som er valgt fra gruppen, der består af tu-mor-nekrosefaktor-alfa (TNF- a), interleukin-6 (IL-6) og interleukin-1 β (IL-1 β).
4. Farmaceutisk sammensætning til anvendelse ifølge et hvilket som helst af de foregående krav, hvor (a) den farmaceutiske sammensætning formuleres til intratracheal administration, såsom ved pulmonal inhalation; parenteral administration; intravenøs administration; eller intraperitoneal administration; eller (b) den farmaceutiske sammensætning omfatter yderligere mindst et yderligere terapeutisk middel.
5. Farmaceutisk sammensætning til anvendelse ifølge krav 4, hvor det yderligere terapeutiske middel: (a) er et glucocorticoid, som er valgt fra gruppen, der består af predni-son, budesonid, mometasonfuroat, fluticasonpropionat, fluticasonfuroat og en kombination deraf, eller (b) er en bronchodilator, som er valgt fra gruppen, der består af en leu-kotrienmodifikator, en anticholinerg bronchodilator, en korttidsvirkende 32-agonist og en langtidsvirkende 32-agonist og en kombination deraf; eller (c) er valgt fra gruppen, der består af et oprenset type-V-kollagen, en IL-13-receptor-antagonist, en proteintyrosinkinase-inhibitor, en endothe- lial-receptor-antagonist, en dobbelt endothelin-receptor-antagonist, en prostacyclin-analog, et anti-CTGF-monoklonalt antistof, en endothelin-receptor-antagonist (A-selektiv), AB0024, et lysyloxidase-lignende 2 (LOXL2)-monoklonalt antistof, en c-Jun N-terminal kinase (JNK)-inhibitor, pirfenidon, IFN-Y1b, et pan-neutraliserende lgG4-humant antistof mod alle tre TGF-3-isoformer, en TGF-3-aktiveringsinhibitor, et rekombinant humant pentraxin-2-protein (rhPTX-2), et bispecifikt IL-4/IL-13-antistof, et humaniseret monoklonalt antistof der er rettet mod inte-grin ανβ6, N-acetylcystein, sildenafil, en tumor-nekrosefaktor (TNF)-antagonist (etanercept) og en kombination deraf; eller (d) er et analgetisk middel eller et anti-infektionsmiddel.
6. Farmaceutisk sammensætning til anvendelse ifølge et hvilket som helst af de foregående krav, hvor bæreren er valgt fra gruppen, der består af en styret frigivelsesbærer, en forsinket frigivelsesbærer, en bærer med vedvarende frigivelse og en bærer med langvarig frigivelse.
7. Farmaceutisk sammensætning til anvendelse ifølge et hvilket som helst af de foregående krav, hvor den terapeutiske mængde af den farmaceutiske sammensætning administreres via en inhalationsindretning der er udvalgt blandt en forstøver, en doseret dosisinhalator (MDI), en tørpulverinhalator (DPI) eller en tø rpu Iverforstøver.
8. Farmaceutisk sammensætning til anvendelsen ifølge krav 7, hvor den farmaceutiske sammensætning er i form af et tørt pulver, der omfatter mikropartikler med massemedian-aerodynamisk diameter (MMAD) på 1 til 5 pm.
DK12771584.5T 2011-04-12 2012-04-12 Sammensætninger og fremgangsmåder til forebyggelse eller behandling af pulmonal fibrose DK2696888T3 (da)

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US201161474370P 2011-04-12 2011-04-12
PCT/US2012/033368 WO2012142320A2 (en) 2011-04-12 2012-04-12 Compositions and methods for preventing or treating diseases, conditions, or processes characterized by aberrant fibroblast proliferation and extracellular matrix deposition

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US (2) US9642888B2 (da)
EP (1) EP2696888B1 (da)
JP (1) JP6031510B2 (da)
KR (1) KR101862291B1 (da)
CN (3) CN108014340A (da)
AU (1) AU2012242768B2 (da)
BR (1) BR112013026313A8 (da)
CA (2) CA2832910C (da)
DK (1) DK2696888T3 (da)
ES (1) ES2711670T3 (da)
HK (1) HK1255005A1 (da)
MX (1) MX359516B (da)
RU (1) RU2620066C2 (da)
SG (2) SG10201604560TA (da)
WO (1) WO2012142320A2 (da)

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CA3042808A1 (en) 2012-10-18
CN104302310A (zh) 2015-01-21
BR112013026313A2 (pt) 2016-12-27
US20190022169A1 (en) 2019-01-24
AU2012242768A1 (en) 2013-10-24
MX2013011771A (es) 2014-07-30
KR20140063517A (ko) 2014-05-27
BR112013026313A8 (pt) 2018-01-30
RU2620066C2 (ru) 2017-05-22
EP2696888B1 (en) 2018-12-05
MX359516B (es) 2018-10-01
CN111110850A (zh) 2020-05-08
US20120263680A1 (en) 2012-10-18
AU2012242768B2 (en) 2017-10-12
CA2832910C (en) 2019-07-02
US9642888B2 (en) 2017-05-09
WO2012142320A2 (en) 2012-10-18
JP2014533235A (ja) 2014-12-11
ES2711670T3 (es) 2019-05-06
SG194135A1 (en) 2013-11-29
WO2012142320A8 (en) 2014-02-20
NZ616672A (en) 2016-04-29
JP6031510B2 (ja) 2016-11-24
RU2013150249A (ru) 2015-05-20
EP2696888A2 (en) 2014-02-19
EP2696888A4 (en) 2016-04-20
HK1255005A1 (zh) 2019-08-02
CN108014340A (zh) 2018-05-11
WO2012142320A3 (en) 2015-06-11
SG10201604560TA (en) 2016-07-28
CA2832910A1 (en) 2012-10-18
KR101862291B1 (ko) 2018-05-29

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