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AR104906A1 - Anticuerpos dirigidos a la proteína morfogenética ósea 9 (bmp9) y métodos a partir de estos - Google Patents

Anticuerpos dirigidos a la proteína morfogenética ósea 9 (bmp9) y métodos a partir de estos

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Publication number
AR104906A1
AR104906A1 ARP160101663A ARP160101663A AR104906A1 AR 104906 A1 AR104906 A1 AR 104906A1 AR P160101663 A ARP160101663 A AR P160101663A AR P160101663 A ARP160101663 A AR P160101663A AR 104906 A1 AR104906 A1 AR 104906A1
Authority
AR
Argentina
Prior art keywords
seq
sequences
lcdr2
hcdr2
hcdr1
Prior art date
Application number
ARP160101663A
Other languages
English (en)
Inventor
Luo Xiao
Xiangyang Lu Chris
Li Qian
Kugler Markus
He Yun
Deng Sujun
Chen Zijun
Huang Dagang
Ulrike Tissot-Daguette Kathrin
Shan Yongqiang
Wu Jing
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of AR104906A1 publication Critical patent/AR104906A1/es

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    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/22Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
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    • A61K31/155Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
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    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
    • A61K31/355Tocopherols, e.g. vitamin E
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
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    • A61K31/575Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
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    • A61K31/7072Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
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  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

Reivindicación 1: Un anticuerpo aislado o su fragmento de unión a antígeno, el cual une a BMP9 humana y comprende: (a) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 21, 22 y 23, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 31, 32 y 33, respectivamente; (b) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 24, 25 y 26, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 34, 35 y 36, respectivamente; (c) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 1, 2 y 3, respectivamente, y. las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 11, 12 y 13, respectivamente; (d) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 4, 5 y 6, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 14, 15 y 16, respectivamente; (e) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 41, 42 y 43, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 51, 52 y 53, respectivamente; (f) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 44, 45 y 46, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 54, 55 y 56, respectivamente; (g) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 61, 62 y 63, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 71, 72 y 73, respectivamente; (h) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 64, 65 y 66, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 74, 75 y 76, respectivamente; (i) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 81, 82 y 83, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 91, 92 y 93, respectivamente; (j) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 84, 85 y 86, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 94, 95 y 96, respectivamente; (k) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 101, 102 y 103, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 111, 112 y 113, respectivamente; (l) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 104, 105 y 106, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 114, 115 y 116, respectivamente; (m) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 121, 122 y 123, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 131, 132 y 133, respectivamente; (n) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 124, 125 y 126, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 134, 135 y 136, respectivamente; (o) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 141, 142 y 143, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 151, 152 y 153, respectivamente; (p) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ 1D Nº 144, 145 y 146, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 154, 155 y 156, respectivamente; (q) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 161, 162 y 163, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 171, 172 y 173, respectivamente; (r) las secuencias HCDR1, HCDR2 y HCDR3 de SEQ ID Nº 164, 165 y 166, respectivamente, y las secuencias LCDR1, LCDR2 y LCDR3 de SEQ ID Nº 174, 175 y 176, respectivamente. Reivindicación 28: Una composición que comprende un anticuerpo aislado o su fragmento de unión a antígeno de cualquiera de las reivindicaciones anteriores, y (a) un vehículo farmacéuticamente aceptable; (b) un agente terapéutico adicional; o (c) combinaciones de los mismos. Reivindicación 44: Un polinucleótido aislado que comprende una secuencia de ácido nucleico que codifica un anticuerpo o su fragmento de unión a antígeno de cualquiera de las reivindicaciones 1 a 27. Reivindicación 58: El uso de un anticuerpo aislado o su fragmento de unión a antígeno de cualquiera de las reivindicaciones 1 - 27, una composición de cualquiera de las reivindicaciones 28 - 32, un polinucleótido aislado de cualquiera de las reivindicaciones 44 - 55, un vector de la reivindicación 56, o una célula de reivindicación 57 en la fabricación de un medicamento.
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BR112017021484A2 (pt) 2018-07-03
US20160355583A1 (en) 2016-12-08
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