WO2012144463A1 - 腫瘍治療剤 - Google Patents
腫瘍治療剤 Download PDFInfo
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- WO2012144463A1 WO2012144463A1 PCT/JP2012/060279 JP2012060279W WO2012144463A1 WO 2012144463 A1 WO2012144463 A1 WO 2012144463A1 JP 2012060279 W JP2012060279 W JP 2012060279W WO 2012144463 A1 WO2012144463 A1 WO 2012144463A1
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- 0 CCNC(Nc(ccc(Oc1c(cc(C(NOC)=O)c(*)c2)c2ncc1)c1)c1Cl)=O Chemical compound CCNC(Nc(ccc(Oc1c(cc(C(NOC)=O)c(*)c2)c2ncc1)c1)c1Cl)=O 0.000 description 1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/47—Quinolines; Isoquinolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/475—Quinolines; Isoquinolines having an indole ring, e.g. yohimbine, reserpine, strychnine, vinblastine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/4353—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Definitions
- the present invention relates to a tumor therapeutic agent using a combination of a compound having a kinase inhibitory action and a compound having a BRAF inhibitory action. More specifically, a compound having a multi-tyrosine kinase inhibitory action and N- (3- ⁇ [5- (4-chlorophenyl) -1H-pyrrolo [2,3-b] pyridin-3-yl] carbonyl ⁇ -2 , 4-difluorophenyl) propane-1-sulfonamide (PLX4032).
- R 1 represents a C 1-6 alkyl group or a C 3-8 cycloalkyl group
- R 2 represents a hydrogen atom or a C 1-6 alkoxy group
- R 3 represents a hydrogen atom or a halogen atom. means.
- the compound represented by formula (I) has an angiogenesis inhibitory action (Patent Document 1) and an inhibitory action on tyrosine kinases (Non-Patent Document 1 to Non-Patent Document 5) reported to be involved in tumor malignancy. (Patent Literature 2 to Patent Literature 5) and the like, and treatment for various tumors such as thyroid cancer, lung cancer, melanoma, endometrial cancer, stomach cancer, bladder cancer, kidney cancer, glioma, liver cancer, ovarian cancer, etc. Known as an agent.
- This compound is called PLX4032, and is currently being developed as a therapeutic agent for tumors such as melanoma.
- tumor therapeutic agents are often not effective for all patients when used alone. So far, attempts have been made to improve the treatment rate by using a plurality of tumor therapeutic agents in combination (Patent Documents 7-9).
- the present inventors have surprisingly exceeded expectations by administering a combination of a compound having the formula (I) and BRAF kinase activity inhibition to a tumor patient.
- the present invention was completed by finding that it has an antitumor effect.
- the present invention provides the following [1] to [8].
- [1] A compound represented by formula (I) or a pharmacologically acceptable salt thereof
- R 1 denotes a C 1-6 alkyl group or a C 3-8 cycloalkyl group.
- R 2 represents a hydrogen atom or a C 1-6 alkoxy group.
- R 3 means a hydrogen atom or a halogen atom.
- a compound represented by formula (II) A therapeutic agent for tumors.
- a tumor therapeutic agent comprising a compound represented by the formula (I) or a pharmacologically acceptable salt thereof and a compound represented by the formula (II).
- a method for treating tumor comprising a combination of a compound represented by the above formula (I) or a pharmacologically acceptable salt thereof and a compound represented by the above formula (II).
- a pharmaceutical composition comprising a compound represented by the above formula (I) or a pharmacologically acceptable salt thereof, a compound represented by the above formula (II) and an excipient.
- a pharmaceutical composition comprising a compound represented by the above formula (I) or a pharmacologically acceptable salt thereof and an excipient, and a medicament comprising a compound represented by the above formula (II) and an excipient
- a kit comprising the composition.
- the compound represented by the above formula (I) is preferably 4- [3-Chloro-4- (cyclopropylaminocarbonyl) aminophenoxy] -7-methoxy-6-quinolinecarboxamide 4- [3-Chloro-4- (methylaminocarbonyl) aminophenoxy] -7-methoxy-6-quinolinecarboxamide 4- [3-Chloro-4- (ethylaminocarbonyl) aminophenoxy] -7-methoxy-6-quinolinecarboxamide N6-methoxy-4- (3-chloro-4- ⁇ [(cyclopropylamino) carbonyl) amino] phenoxy ⁇ -7-methoxy-6-quinolinecarboxamide And N6-methoxy-4- (3-chloro-4- ⁇ [(ethylamino) carbonyl] amino ⁇ phenoxy) -7-methoxy-6-quinolinecarboxamide
- the present invention provides a tumor therapeutic agent using a combination of a compound having a multi-tyrosine kinase inhibitory action and a compound having BRAF kinase activity inhibition.
- a tumor therapeutic agent exhibits a remarkable antitumor effect as compared with the case of using it alone, and also exhibits an antitumor effect against various cancer types.
- the compound represented by formula (I) or a pharmacologically acceptable salt thereof according to the present invention can be produced by the method described in Patent Document 1. Further, the compound represented by the formula (II) according to the present invention (hereinafter simply referred to as PLX4032) can be produced by the method described in Patent Document 6.
- Such compounds include 4- ⁇ 4-[( ⁇ [4-chloro-3- (trifluoromethyl) phenyl] amino ⁇ carbonyl) amino] phenoxy ⁇ -N-methylpyridine-2-carboxamide 4-methylbenzenesulfurate.
- Sorafenib, RAF-265, SB-590885, aminoisoquinoline and PF-0419789 are disclosed in WO 2000/041698, US Patent Application Publication No. 2007-0049622, WO 2002/024680, WO It can be produced by the methods described in 2008/153947 and WO2007 / 105058.
- Examples of the pharmacologically acceptable salt include a salt with an inorganic acid, a salt with an organic acid, a salt with an inorganic base, a salt with an organic base, and a salt with an acidic or basic amino acid.
- salts with inorganic acid include salts with hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like.
- salts with organic acids include acetic acid, succinic acid, fumaric acid, maleic acid, tartaric acid, citric acid, lactic acid, stearic acid, benzoic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid. And salt.
- the salt with an inorganic base include alkali metal salts such as sodium salt and potassium salt, alkaline earth metal salts such as calcium salt and magnesium salt, aluminum salt and ammonium salt.
- the salt with an organic base include salts with diethylamine, diethanolamine, meglumine, N, N-dibenzylethylenediamine and the like.
- Preferable examples of the salt with acidic amino acid include salts with aspartic acid, glutamic acid and the like.
- Preferable examples of the salt with basic amino acid include salts with arginine, lysine, ornithine and the like.
- Particularly preferred pharmacologically acceptable salts are salts with organic acids.
- the tumor therapeutic agent of the present invention can be orally administered in the form of solid preparations such as tablets, granules, fine granules, powders, capsules or the like, liquids, jellies, syrups and the like.
- tumor therapeutic agent of the present invention may be administered parenterally in the form of injections, suppositories, ointments, cataplasms and the like.
- the dose of the compound represented by the formula (I) or a pharmacologically acceptable salt thereof is the degree of symptoms, patient age, sex, body weight, sensitivity difference, administration method, administration timing, administration interval, pharmaceutical preparation. Depending on the type, etc., it can be selected as appropriate. Usually, when administered orally to an adult (body weight 60 kg), it is 1 to 600 mg, preferably 5 to 400 mg, more preferably 5 to 200 mg per day. This can be administered in 1 to 3 divided doses per day.
- the dose of PLX4032 can be appropriately selected as described above.
- the daily dose is 1 to 2000 mg, preferably 100 to 1500 mg, more preferably 240 to 1200 mg. This can be administered in 1 to 3 divided doses per day.
- the main agent ie, the compound represented by the formula (I) or a pharmacologically acceptable salt thereof and PLX4032, an excipient, and optionally a binder, a disintegrant, a lubricant.
- Examples of the excipient include lactose, corn starch, sucrose, glucose, sorbitol, crystalline cellulose, silicon dioxide and the like.
- Examples of the binder include polyvinyl alcohol, ethyl cellulose, methyl cellulose, gum arabic, hydroxypropyl cellulose, hydroxypropyl methyl cellulose and the like.
- Examples of the lubricant include magnesium stearate, talc, and silica.
- Examples of the colorant include titanium oxide, iron sesquioxide, yellow iron sesquioxide, cochineal, carmine, and riboflavin.
- Examples of flavoring agents include cocoa powder, ascorbic acid, tartaric acid, mint oil, borneol, and cinnamon powder. These tablets and granules may be coated as necessary.
- suspending agent examples include methyl cellulose, polysorbate 80, hydroxyethyl cellulose, gum arabic, tragacanth powder, sodium carboxymethyl cellulose, polyoxyethylene sorbitan monolaurate and the like.
- solubilizer examples include polyoxyethylene hydrogenated castor oil, polysorbate 80, nicotinamide, polyoxyethylene sorbitan monolaurate, macrogol, and glycerin fatty acid ester.
- Examples of the stabilizer include sodium sulfite and sodium metasulfite.
- Examples of the preservative include methyl paraoxybenzoate, ethyl paraoxybenzoate, sorbic acid, phenol, cresol, chlorocresol and the like.
- the compound represented by formula (I) or a pharmacologically acceptable salt thereof and PLX4032 may be formulated separately, and both may be administered simultaneously or separately. Moreover, it is good also as what is called a kit formulation by putting two formulations in one package. Furthermore, both compounds may be contained in one preparation.
- the type of tumor to be treated with the tumor therapeutic agent of the present invention is not particularly limited.
- Human-derived melanoma cell line A375 was suspended in PBS (Wako Pure Chemical Industries, Ltd.) to a concentration of 5 ⁇ 10 6 cells / ml and mixed well. 0.1 mL of the mixture was transplanted into the right flank subcutaneous part of each mouse.
- Tumor volume (mm 3 ) major axis (mm) ⁇ minor axis (mm) ⁇ minor axis (mm) / 2
- Compound A was dissolved in purified water to a concentration of 1 mg / mL.
- PLX4032 was dissolved in DMSO to a concentration of 200 mg / ml. Further, this solution was diluted 20-fold with a 1% aqueous methylcellulose solution to prepare a 10 mg / mL PLX4032 suspension.
- a control group, a compound A group, a PLX4032 group, and a compound A and PLX4032 combination group (hereinafter referred to as a combination group) were set.
- Mice of Compound A or PLX4032 were orally administered once daily with Compound A aqueous solution or PLX4032 suspension at 10 mL / kg. Both drug solutions were orally administered to mice in the combination group once a day at 10 mL / kg each. The administration period was 23 days. In addition, administration was not performed to the mouse
- the tumor volume was measured on the administration start date and on days 2, 5, 7, 9, 12, 14, 16, 19, 21, and 23 after the start of administration.
- the ratio of the tumor volume on each measurement day to the tumor volume on the start day of administration was calculated as a specific tumor volume (hereinafter referred to as RTV).
- RTV specific tumor volume
- the average value of RTV in each group of mice was calculated.
- the daily changes are shown in Table 1 and FIG. 1, and the values for each group on the 23rd day are shown in FIG.
Abstract
Description
[1] 式(I)で表される化合物またはその薬理学的に許容される塩
[式中、R1はC1-6アルキル基またはC3-8シクロアルキル基を意味する。R2は水素原子またはC1-6アルコキシ基を意味する。R3は水素原子またはハロゲン原子を意味する。]
および式(II)で表される化合物
を併用する腫瘍治療剤。
[2] 上記式(I)で表される化合物またはその薬理学的に許容される塩および上記式(II)で表される化合物を同時にまたは別々に投与する腫瘍治療剤。
[3] 上記式(I)で表される化合物またはその薬理学的に許容される塩および上記式(II)で表される化合物を含む腫瘍治療剤。
[4] 上記式(I)で表される化合物またはその薬理学的に許容される塩と併用することによる腫瘍治療のための上記式(II)で表される化合物。
[5] 上記式(II)で表される化合物と併用することによる腫瘍治療のための上記式(I)で表される化合物またはその薬理学的に許容される塩。
[6] 上記式(I)で表される化合物またはその薬理学的に許容される塩および上記式(II)で表される化合物を併用する腫瘍の治療方法。
[7] 上記式(I)で表される化合物またはその薬理学的に許容される塩、上記式(II)で表される化合物および賦形剤を含む医薬組成物。
[8] 上記式(I)で表される化合物またはその薬理学的に許容される塩および賦形剤を含む医薬組成物と上記式(II)で表される化合物および賦形剤を含む医薬組成物とを含むキット。
4-[3-クロロ-4-(シクロプロピルアミノカルボニル)アミノフェノキシ]-7-メトキシ-6-キノリンカルボキサミド
4-[3-クロロ-4-(メチルアミノカルボニル)アミノフェノキシ]-7-メトキシ-6-キノリンカルボキサミド
4-[3-クロロ-4-(エチルアミノカルボニル)アミノフェノキシ]-7-メトキシ-6-キノリンカルボキサミド
N6-メトキシ-4-(3-クロロ-4-{[(シクロプロピルアミノ)カルボニル)アミノ]フェノキシ}-7-メトキシ-6-キノリンカルボキサミド
および
N6-メトキシ-4-(3-クロロ-4-{[(エチルアミノ)カルボニル]アミノ}フェノキシ)-7-メトキシ-6-キノリンカルボキサミド
からなる群から選択される1種以上の化合物であり、
より好ましくは、
4-[3-クロロ-4-(シクロプロピルアミノカルボニル)アミノフェノキシ]-7-メトキシ-6-キノリンカルボキシアミド
である(以下、化合物Aと表記することがある)。
1-メチル-5-({2-[4-(トリフルオロメチル)-1H-イミダゾール-2-イル]ピリジン-4-イル}オキシ)-N-[4-(トリフルオロメチル)フェニル]-1H-ベンズイミダゾール-2-アミン(RAF-265)
5-(2-{4-[2-(ジメチルアミノ)エトキシ]フェニル}-4-ピリジン-4-イル-1H-イミダゾール-5-イル)インダン-1-オン オキシム(SB-590885)
1-N-(4-クロロフェニル)-6-メチル-5-N-[3-(9H-プリン-6-イル)ピリジン-2-イル]イソキノリン-1,5-ジアミン(以下、アミノイソキノリンと略す)
および
[3-(3-ヒドロキシ-5-メチルフェニル)-4-(2-{[(2S)-2-ヒドロキシプロピル]アミノ}ピリミジン-4-イル)-1H-ピラゾール-1-イル]アセトニトリル(PF-0419789)
等が挙げられる。
ソラフェニブ、RAF-265、SB-590885、アミノイソキノリンおよびPF-0419789は、それぞれ国際公開第2000/041698号、米国特許出願公開第2007-0049622号明細書、国際公開第2002/024680号、国際公開第2008/153947号および国際公開第2007/105058号に記載された方法により製造することができる。
各群5例のヌードマウス(CAnN.Cg-Foxn1nu/CrlCrlj、雌、日本チャールズリバー株式会社)を使用して、化合物A、PLX4032または両化合物を投与した場合の抗腫瘍効果を評価した。ヒト由来のメラノーマ細胞株A375(ATCC)を、PBS(和光純薬工業株式会社)に、5×106個/mlの濃度となるように懸濁し、十分に混和した。その混和液を各マウスの右脇腹皮下部に、0.1mLずつ移植した。移植から14日後に、腫瘍の長径および短径を電子デジタルノギス(デジマチックTMキャリパ、株式会社ミツトヨ)で測定した。各群の腫瘍体積の平均値がほぼ等しくなるように、マウスを群分けした。なお、腫瘍の体積を、以下の式に従って算出した。
腫瘍体積(mm3)=長径(mm)×短径(mm)×短径(mm)/2
Claims (5)
- 式(I)で表される化合物が、
4-[3-クロロ-4-(シクロプロピルアミノカルボニル)アミノフェノキシ]-7-メトキシ-6-キノリンカルボキサミド
4-[3-クロロ-4-(メチルアミノカルボニル)アミノフェノキシ]-7-メトキシ-6-キノリンカルボキサミド
4-[3-クロロ-4-(エチルアミノカルボニル)アミノフェノキシ]-7-メトキシ-6-キノリンカルボキサミド
N6-メトキシ-4-(3-クロロ-4-{[(シクロプロピルアミノ)カルボニル)アミノ]フェノキシ}-7-メトキシ-6-キノリンカルボキサミド
および
N6-メトキシ-4-(3-クロロ-4-{[(エチルアミノ)カルボニル]アミノ}フェノキシ)-7-メトキシ-6-キノリンカルボキサミド
からなる群から選択される1種以上の化合物である、請求項1~3のいずれか一項に記載の腫瘍治療剤。
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020137020616A KR101762999B1 (ko) | 2011-04-18 | 2012-04-16 | 종양 치료제 |
US14/002,018 US8962650B2 (en) | 2011-04-18 | 2012-04-16 | Therapeutic agent for tumor |
BR112013021941-6A BR112013021941B1 (pt) | 2011-04-18 | 2012-04-16 | Agente terapêutico para tumor |
RU2013140169/15A RU2580609C2 (ru) | 2011-04-18 | 2012-04-16 | Противоопухолевое терапевтическое средство |
EP12774278.1A EP2700403B1 (en) | 2011-04-18 | 2012-04-16 | Therapeutic agent for tumor |
JP2013510994A JP6021805B2 (ja) | 2011-04-18 | 2012-04-16 | 腫瘍治療剤 |
CA2828946A CA2828946C (en) | 2011-04-18 | 2012-04-16 | Therapeutic agent for tumor |
CN201280010898.XA CN103402519B (zh) | 2011-04-18 | 2012-04-16 | 肿瘤治疗剂 |
MX2013009931A MX2013009931A (es) | 2011-04-18 | 2012-04-16 | Agentes terapeuticos contra tumores. |
AU2012246490A AU2012246490B2 (en) | 2011-04-18 | 2012-04-16 | Therapeutic agent for tumor |
IL227558A IL227558A (en) | 2011-04-18 | 2013-07-18 | A therapeutic factor for tumors |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011091969 | 2011-04-18 | ||
JP2011-091969 | 2011-04-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012144463A1 true WO2012144463A1 (ja) | 2012-10-26 |
Family
ID=47041569
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2012/060279 WO2012144463A1 (ja) | 2011-04-18 | 2012-04-16 | 腫瘍治療剤 |
Country Status (12)
Country | Link |
---|---|
US (1) | US8962650B2 (ja) |
EP (1) | EP2700403B1 (ja) |
JP (1) | JP6021805B2 (ja) |
KR (1) | KR101762999B1 (ja) |
CN (1) | CN103402519B (ja) |
AU (1) | AU2012246490B2 (ja) |
BR (1) | BR112013021941B1 (ja) |
CA (1) | CA2828946C (ja) |
IL (1) | IL227558A (ja) |
MX (1) | MX2013009931A (ja) |
RU (1) | RU2580609C2 (ja) |
WO (1) | WO2012144463A1 (ja) |
Cited By (10)
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Also Published As
Publication number | Publication date |
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EP2700403A1 (en) | 2014-02-26 |
RU2013140169A (ru) | 2015-05-27 |
CA2828946A1 (en) | 2012-10-26 |
CN103402519B (zh) | 2015-11-25 |
JPWO2012144463A1 (ja) | 2014-07-28 |
US8962650B2 (en) | 2015-02-24 |
KR101762999B1 (ko) | 2017-07-28 |
RU2580609C2 (ru) | 2016-04-10 |
BR112013021941B1 (pt) | 2022-11-16 |
BR112013021941A2 (pt) | 2016-11-16 |
EP2700403A4 (en) | 2014-09-17 |
KR20140035334A (ko) | 2014-03-21 |
IL227558A (en) | 2017-07-31 |
AU2012246490B2 (en) | 2016-08-04 |
CA2828946C (en) | 2016-06-21 |
US20140031384A1 (en) | 2014-01-30 |
EP2700403B1 (en) | 2015-11-25 |
CN103402519A (zh) | 2013-11-20 |
IL227558A0 (en) | 2013-09-30 |
AU2012246490A1 (en) | 2013-08-01 |
JP6021805B2 (ja) | 2016-11-09 |
MX2013009931A (es) | 2013-10-01 |
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