PE20220965A1 - Analogos de relaxina y metodos para usarlos - Google Patents

Analogos de relaxina y metodos para usarlos

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Publication number
PE20220965A1
PE20220965A1 PE2022000147A PE2022000147A PE20220965A1 PE 20220965 A1 PE20220965 A1 PE 20220965A1 PE 2022000147 A PE2022000147 A PE 2022000147A PE 2022000147 A PE2022000147 A PE 2022000147A PE 20220965 A1 PE20220965 A1 PE 20220965A1
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PE
Peru
Prior art keywords
seq
vhh
sequence selected
nos
relaxin
Prior art date
Application number
PE2022000147A
Other languages
English (en)
Inventor
Stacey Lynn Lee
Petra Verdino
Xiaojun Wang
Original Assignee
Lilly Co Eli
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Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of PE20220965A1 publication Critical patent/PE20220965A1/es

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    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575Hormones
    • C07K14/62Insulins
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    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575Hormones
    • C07K14/64Relaxins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/13Amines
    • A61K31/155Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/4261,3-Thiazoles
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    • 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
    • A61K38/22Hormones
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    • 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
    • A61K38/22Hormones
    • A61K38/28Insulins
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    • 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
    • A61K38/22Hormones
    • A61K38/30Insulin-like growth factors, i.e. somatomedins, e.g. IGF-1, IGF-2
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    • 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
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    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
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    • A61K47/62Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/65Peptidic linkers, binders or spacers, e.g. peptidic enzyme-labile linkers
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    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6801Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
    • A61K47/6803Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
    • A61K47/6811Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being a protein or peptide, e.g. transferrin or bleomycin
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    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6835Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
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    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2863Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators
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    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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    • C07K2317/569Single domain, e.g. dAb, sdAb, VHH, VNAR or nanobody®
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Obesity (AREA)
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  • Urology & Nephrology (AREA)
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  • Child & Adolescent Psychology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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Abstract

Se divulgan compuestos analogos de relaxina (RLN) que comprende una estructura de VHH-L1-A-L2-B, VHH-L1-B-L2-A, A-L2-B-L1-VHH o B-L2-A-L1-VHH; en donde VHH comprende una secuencia de aminoacidos seleccionada de SEQ ID NOS: 10, 11, 12 y 13; A es una cadena A de relaxina que comprende una secuencia seleccionada de SEQ ID NOS: 2, 5 y 8; B es una cadena B de relaxina que comprende una secuencia seleccionada de SEQ ID NOS: 3, 6 y 9; L1 es un primer ligador que comprende una secuencia seleccionada de (GGGGQ)n (SEQ ID NO:14), (PGPQ)n (SEQ ID NO:17) y (PGPA)n (SEQ ID NO:18), y en donde n puede ser de 1 a 10 y L2 es un segundo ligador que comprende la secuencia seleccionada del grupo que consiste en SEQ ID NOS: 22, 23 y 67. Dichos compuestos analogos aumentan la semivida en comparacion con la RLN humana nativa, mantienen la selectividad para el receptor RXFP1 y proporcionan estabilidad in vitro e in vivo para mejorar las propiedades farmacologicas y reducir la inmunogenicidad. Tambien refiere composiciones farmaceuticas que los contiene siendo utiles para el tratamiento de afecciones, enfermedades o trastornos cardiovasculares, pulmonares y/o renales.
PE2022000147A 2019-07-31 2020-07-31 Analogos de relaxina y metodos para usarlos PE20220965A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962880968P 2019-07-31 2019-07-31
US202062970005P 2020-02-04 2020-02-04
PCT/US2020/044462 WO2021022139A1 (en) 2019-07-31 2020-07-31 Relaxin analogs and methods of using the same

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Publication Number Publication Date
PE20220965A1 true PE20220965A1 (es) 2022-06-10

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US (2) US20220378931A1 (es)
EP (2) EP4004027A1 (es)
JP (3) JP7270105B2 (es)
KR (1) KR20220031044A (es)
CN (2) CN114174347A (es)
AU (1) AU2020321977C1 (es)
BR (1) BR112022001448A2 (es)
CA (2) CA3144989A1 (es)
CL (1) CL2022000178A1 (es)
CO (1) CO2022000656A2 (es)
CR (1) CR20220021A (es)
DO (1) DOP2022000018A (es)
EC (1) ECSP22007726A (es)
IL (1) IL289464A (es)
JO (1) JOP20220023A1 (es)
MX (1) MX2022001136A (es)
PE (1) PE20220965A1 (es)
TW (1) TW202120536A (es)
WO (2) WO2021022149A1 (es)

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