CA2824092C - Use of alk inhibitors for the treatment of eml4-alk+ non-small cell lung cancer - Google Patents
Use of alk inhibitors for the treatment of eml4-alk+ non-small cell lung cancer Download PDFInfo
- Publication number
- CA2824092C CA2824092C CA2824092A CA2824092A CA2824092C CA 2824092 C CA2824092 C CA 2824092C CA 2824092 A CA2824092 A CA 2824092A CA 2824092 A CA2824092 A CA 2824092A CA 2824092 C CA2824092 C CA 2824092C
- Authority
- CA
- Canada
- Prior art keywords
- compound
- phenyl
- alk
- eml4
- lung cancer
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
- 208000002154 non-small cell lung carcinoma Diseases 0.000 title claims abstract description 72
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 title claims abstract description 72
- 238000011282 treatment Methods 0.000 title claims description 37
- 239000003112 inhibitor Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 135
- 150000003839 salts Chemical class 0.000 claims description 56
- 206010028980 Neoplasm Diseases 0.000 claims description 40
- 239000008194 pharmaceutical composition Substances 0.000 claims description 31
- 239000003814 drug Substances 0.000 claims description 29
- 239000003937 drug carrier Substances 0.000 claims description 25
- 238000004519 manufacturing process Methods 0.000 claims description 25
- 239000002146 L01XE16 - Crizotinib Substances 0.000 claims description 18
- KTEIFNKAUNYNJU-GFCCVEGCSA-N crizotinib Chemical compound O([C@H](C)C=1C(=C(F)C=CC=1Cl)Cl)C(C(=NC=1)N)=CC=1C(=C1)C=NN1C1CCNCC1 KTEIFNKAUNYNJU-GFCCVEGCSA-N 0.000 claims description 18
- 229960005061 crizotinib Drugs 0.000 claims description 18
- 125000003386 piperidinyl group Chemical group 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000005842 heteroatom Chemical group 0.000 claims description 9
- 241001465754 Metazoa Species 0.000 claims description 8
- 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 4
- 201000011510 cancer Diseases 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 10
- VOASCOSDVNWJEV-UHFFFAOYSA-N 5-chloro-2-n-(5-methyl-4-piperidin-2-yl-2-propan-2-yloxyphenyl)-4-n-(2-propan-2-ylsulfonylphenyl)pyrimidine-2,4-diamine Chemical compound CC=1C=C(NC=2N=C(NC=3C(=CC=CC=3)S(=O)(=O)C(C)C)C(Cl)=CN=2)C(OC(C)C)=CC=1C1CCCCN1 VOASCOSDVNWJEV-UHFFFAOYSA-N 0.000 claims 4
- IGUPHIBNKHHSSE-UHFFFAOYSA-N 5-chloro-2-n-(5-methyl-4-piperidin-3-yl-2-propan-2-yloxyphenyl)-4-n-(2-propan-2-ylsulfonylphenyl)pyrimidine-2,4-diamine Chemical compound CC=1C=C(NC=2N=C(NC=3C(=CC=CC=3)S(=O)(=O)C(C)C)C(Cl)=CN=2)C(OC(C)C)=CC=1C1CCCNC1 IGUPHIBNKHHSSE-UHFFFAOYSA-N 0.000 claims 4
- VOASCOSDVNWJEV-JOCHJYFZSA-N 5-chloro-2-n-[5-methyl-4-[(2r)-piperidin-2-yl]-2-propan-2-yloxyphenyl]-4-n-(2-propan-2-ylsulfonylphenyl)pyrimidine-2,4-diamine Chemical compound CC=1C=C(NC=2N=C(NC=3C(=CC=CC=3)S(=O)(=O)C(C)C)C(Cl)=CN=2)C(OC(C)C)=CC=1[C@H]1CCCCN1 VOASCOSDVNWJEV-JOCHJYFZSA-N 0.000 claims 4
- VOASCOSDVNWJEV-QFIPXVFZSA-N 5-chloro-2-n-[5-methyl-4-[(2s)-piperidin-2-yl]-2-propan-2-yloxyphenyl]-4-n-(2-propan-2-ylsulfonylphenyl)pyrimidine-2,4-diamine Chemical compound CC=1C=C(NC=2N=C(NC=3C(=CC=CC=3)S(=O)(=O)C(C)C)C(Cl)=CN=2)C(OC(C)C)=CC=1[C@@H]1CCCCN1 VOASCOSDVNWJEV-QFIPXVFZSA-N 0.000 claims 4
- VERWOWGGCGHDQE-UHFFFAOYSA-N ceritinib Chemical compound CC=1C=C(NC=2N=C(NC=3C(=CC=CC=3)S(=O)(=O)C(C)C)C(Cl)=CN=2)C(OC(C)C)=CC=1C1CCNCC1 VERWOWGGCGHDQE-UHFFFAOYSA-N 0.000 claims 4
- BPMAKGFLDNAAQC-UHFFFAOYSA-N 6-[[5-chloro-4-(2-propan-2-ylsulfonylanilino)pyrimidin-2-yl]amino]-2-(1-methylpiperidin-4-yl)-5-propan-2-yloxy-3h-isoindol-1-one Chemical compound O=C1C=2C=C(NC=3N=C(NC=4C(=CC=CC=4)S(=O)(=O)C(C)C)C(Cl)=CN=3)C(OC(C)C)=CC=2CN1C1CCN(C)CC1 BPMAKGFLDNAAQC-UHFFFAOYSA-N 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- YAAWASYJIRZXSZ-UHFFFAOYSA-N pyrimidine-2,4-diamine Chemical compound NC1=CC=NC(N)=N1 YAAWASYJIRZXSZ-UHFFFAOYSA-N 0.000 description 19
- 210000004027 cell Anatomy 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 241000699666 Mus <mouse, genus> Species 0.000 description 6
- 241000699670 Mus sp. Species 0.000 description 6
- 230000000259 anti-tumor effect Effects 0.000 description 6
- 230000001404 mediated effect Effects 0.000 description 6
- 229940125904 compound 1 Drugs 0.000 description 5
- 101150023956 ALK gene Proteins 0.000 description 4
- 230000010261 cell growth Effects 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- 238000002513 implantation Methods 0.000 description 4
- 210000001519 tissue Anatomy 0.000 description 4
- 102100033793 ALK tyrosine kinase receptor Human genes 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 230000004663 cell proliferation Effects 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 201000005202 lung cancer Diseases 0.000 description 3
- 208000020816 lung neoplasm Diseases 0.000 description 3
- 108010082117 matrigel Proteins 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 description 2
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 2
- 230000003350 DNA copy number gain Effects 0.000 description 2
- 102100027100 Echinoderm microtubule-associated protein-like 4 Human genes 0.000 description 2
- 101710203446 Echinoderm microtubule-associated protein-like 4 Proteins 0.000 description 2
- 108060001084 Luciferase Proteins 0.000 description 2
- 239000005089 Luciferase Substances 0.000 description 2
- 206010029260 Neuroblastoma Diseases 0.000 description 2
- 239000012980 RPMI-1640 medium Substances 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 230000003321 amplification Effects 0.000 description 2
- 210000000349 chromosome Anatomy 0.000 description 2
- 239000012091 fetal bovine serum Substances 0.000 description 2
- 230000002068 genetic effect Effects 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 230000035772 mutation Effects 0.000 description 2
- 238000003199 nucleic acid amplification method Methods 0.000 description 2
- 230000008707 rearrangement Effects 0.000 description 2
- 239000012679 serum free medium Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 1
- 229940126069 ALK kinase inhibitor Drugs 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 231100001273 GLP toxicology study Toxicity 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 229940125895 MET kinase inhibitor Drugs 0.000 description 1
- 241000699660 Mus musculus Species 0.000 description 1
- 238000002123 RNA extraction Methods 0.000 description 1
- 239000006146 Roswell Park Memorial Institute medium Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 208000036142 Viral infection Diseases 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 231100000504 carcinogenesis Toxicity 0.000 description 1
- 238000002701 cell growth assay Methods 0.000 description 1
- 238000001516 cell proliferation assay Methods 0.000 description 1
- 230000000973 chemotherapeutic effect Effects 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 231100000517 death Toxicity 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 210000005260 human cell Anatomy 0.000 description 1
- 208000026278 immune system disease Diseases 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000001613 neoplastic effect Effects 0.000 description 1
- 238000011580 nude mouse model Methods 0.000 description 1
- 238000003305 oral gavage Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- 238000012447 xenograft mouse model Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161438878P | 2011-02-02 | 2011-02-02 | |
| US61/438,878 | 2011-02-02 | ||
| PCT/US2012/023669 WO2012106540A1 (en) | 2011-02-02 | 2012-02-02 | Methods of using alk inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2824092A1 CA2824092A1 (en) | 2012-08-09 |
| CA2824092C true CA2824092C (en) | 2020-06-30 |
Family
ID=45582065
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2824092A Active CA2824092C (en) | 2011-02-02 | 2012-02-02 | Use of alk inhibitors for the treatment of eml4-alk+ non-small cell lung cancer |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8703787B2 (OSRAM) |
| EP (1) | EP2670401B1 (OSRAM) |
| JP (1) | JP5837095B2 (OSRAM) |
| KR (1) | KR101521861B1 (OSRAM) |
| CN (1) | CN103458881B (OSRAM) |
| AU (1) | AU2012212142B2 (OSRAM) |
| BR (1) | BR112013019643B1 (OSRAM) |
| CA (1) | CA2824092C (OSRAM) |
| CY (1) | CY1116662T1 (OSRAM) |
| DK (1) | DK2670401T3 (OSRAM) |
| EA (1) | EA023404B1 (OSRAM) |
| ES (1) | ES2543567T3 (OSRAM) |
| HR (1) | HRP20150946T1 (OSRAM) |
| HU (1) | HUE025395T2 (OSRAM) |
| ME (1) | ME02200B (OSRAM) |
| MX (1) | MX2013008791A (OSRAM) |
| PL (1) | PL2670401T3 (OSRAM) |
| PT (1) | PT2670401E (OSRAM) |
| RS (1) | RS54189B1 (OSRAM) |
| SI (1) | SI2670401T1 (OSRAM) |
| SM (1) | SMT201500300B (OSRAM) |
| WO (1) | WO2012106540A1 (OSRAM) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102156398B1 (ko) | 2012-11-06 | 2020-09-15 | 상하이 포천 파마슈티컬 씨오 엘티디 | Ａｌｋ 키나아제 억제제 |
| IN2015DN04175A (OSRAM) * | 2012-11-07 | 2015-10-16 | Novartis Ag | |
| CN104109149B (zh) * | 2013-04-22 | 2018-09-28 | 苏州泽璟生物制药有限公司 | 氘代的二氨基嘧啶化合物以及包含该化合物的药物组合物 |
| ITMI20131124A1 (it) * | 2013-07-04 | 2015-01-05 | Univ Milano Bicocca | 2-acilamminotiazoli per il trattamento del cancro |
| WO2015003658A1 (en) * | 2013-07-11 | 2015-01-15 | Betta Pharmaceuticals Co., Ltd | Protein tyrosine kinase modulators and methods of use |
| JP6479812B2 (ja) * | 2013-08-28 | 2019-03-06 | ノバルティス アーゲー | 細胞増殖性疾患を治療するためのａｌｋ阻害剤とｃｄｋ阻害剤との組合せ |
| CN104672214B (zh) * | 2013-12-03 | 2019-04-12 | 上海翰森生物医药科技有限公司 | 具有alk抑制活性的化合物及其制备与用途 |
| MX2016008362A (es) * | 2013-12-23 | 2016-09-08 | Novartis Ag | Combinaciones farmaceuticas. |
| CN104876914B (zh) * | 2014-02-28 | 2017-04-19 | 山东轩竹医药科技有限公司 | 嘧啶衍生物类间变性淋巴瘤激酶抑制剂 |
| KR101656382B1 (ko) * | 2014-02-28 | 2016-09-09 | 한국화학연구원 | 피리미딘-2,4-디아민 유도체 및 이를 유효성분으로 함유하는 항암용 약학적 조성물 |
| KR101733733B1 (ko) * | 2014-06-17 | 2017-05-11 | 한국화학연구원 | 피리미딘-2,4-디아민 유도체 및 이를 유효성분으로 함유하는 항암용 약학적 조성물 |
| CN105524045B (zh) * | 2014-10-22 | 2020-04-10 | 山东轩竹医药科技有限公司 | 四环类间变性淋巴瘤激酶抑制剂 |
| CN106146525B (zh) * | 2015-04-10 | 2018-11-02 | 山东轩竹医药科技有限公司 | 三并环类间变性淋巴瘤激酶抑制剂 |
| US10259816B2 (en) | 2015-04-24 | 2019-04-16 | Guangzhou Maxinovel Pharmaceuticals Co., Ltd. | Condensed-ring pyrimidylamino derivative, preparation method therefor, and intermediate, pharmaceutical composition and applications thereof |
| CN106699743B (zh) | 2015-11-05 | 2020-06-12 | 湖北生物医药产业技术研究院有限公司 | 嘧啶类衍生物及其用途 |
| CN106220608B (zh) * | 2016-07-25 | 2018-11-27 | 安润医药科技（苏州）有限公司 | 二苯氨基嘧啶及三嗪化合物、其药用组合物及用途 |
| CN107698603B (zh) * | 2016-08-09 | 2022-04-08 | 南京红云生物科技有限公司 | 噻吩并嘧啶类化合物、其制备方法、药用组合物及其应用 |
| CN109715620B (zh) * | 2016-08-29 | 2022-05-06 | 密歇根大学董事会 | 作为alk抑制剂的氨基嘧啶 |
| CN111484484B (zh) * | 2020-04-13 | 2021-11-23 | 沈阳药科大学 | 含芳杂环的2,4-二芳氨基嘧啶衍生物及其制备与应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9311920D0 (en) | 1993-06-09 | 1993-07-28 | Pfizer Ltd | Therapeutic agents |
| GB0305929D0 (en) | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
| JP4607879B2 (ja) * | 2003-08-15 | 2011-01-05 | ノバルティス アーゲー | 新生物疾患、炎症および免疫障害の処置に有用な２，４−ピリミジンジアミン |
| GB0419161D0 (en) * | 2004-08-27 | 2004-09-29 | Novartis Ag | Organic compounds |
| ES2444222T3 (es) | 2006-07-10 | 2014-02-24 | Goji Limited | Preparación de alimentos |
| CA2598893C (en) * | 2006-10-11 | 2012-04-10 | Astellas Pharma Inc. | Eml4-alk fusion gene |
| RS53588B1 (sr) * | 2006-12-08 | 2015-02-27 | Irm Llc | Jedinjenja i kompozicije kao inhibitori protein kinaza |
| BRPI0720264B1 (pt) * | 2006-12-08 | 2022-03-03 | Novartis Ag | Compostos e composições como inibidores de proteína cinase |
| CA2720946C (en) * | 2008-04-07 | 2013-05-28 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
-
2012
- 2012-02-02 ME MEP-2015-127A patent/ME02200B/me unknown
- 2012-02-02 PT PT127036705T patent/PT2670401E/pt unknown
- 2012-02-02 ES ES12703670.5T patent/ES2543567T3/es active Active
- 2012-02-02 DK DK12703670.5T patent/DK2670401T3/en active
- 2012-02-02 HR HRP20150946TT patent/HRP20150946T1/hr unknown
- 2012-02-02 CA CA2824092A patent/CA2824092C/en active Active
- 2012-02-02 EP EP12703670.5A patent/EP2670401B1/en active Active
- 2012-02-02 CN CN201280007465.9A patent/CN103458881B/zh active Active
- 2012-02-02 BR BR112013019643-2A patent/BR112013019643B1/pt active IP Right Grant
- 2012-02-02 WO PCT/US2012/023669 patent/WO2012106540A1/en not_active Ceased
- 2012-02-02 AU AU2012212142A patent/AU2012212142B2/en active Active
- 2012-02-02 MX MX2013008791A patent/MX2013008791A/es unknown
- 2012-02-02 PL PL12703670T patent/PL2670401T3/pl unknown
- 2012-02-02 HU HUE12703670A patent/HUE025395T2/en unknown
- 2012-02-02 SI SI201230285T patent/SI2670401T1/sl unknown
- 2012-02-02 US US13/981,046 patent/US8703787B2/en active Active
- 2012-02-02 RS RS20150563A patent/RS54189B1/sr unknown
- 2012-02-02 KR KR1020137023001A patent/KR101521861B1/ko active Active
- 2012-02-02 EA EA201391114A patent/EA023404B1/ru not_active IP Right Cessation
- 2012-02-02 JP JP2013552637A patent/JP5837095B2/ja active Active
-
2015
- 2015-08-28 CY CY20151100758T patent/CY1116662T1/el unknown
- 2015-11-30 SM SM201500300T patent/SMT201500300B/it unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUE025395T2 (en) | 2016-02-29 |
| PT2670401E (pt) | 2015-10-12 |
| EA201391114A1 (ru) | 2013-12-30 |
| CN103458881B (zh) | 2015-08-12 |
| SMT201500300B (it) | 2016-01-08 |
| MX2013008791A (es) | 2013-10-07 |
| DK2670401T3 (en) | 2015-09-07 |
| KR20130121174A (ko) | 2013-11-05 |
| WO2012106540A1 (en) | 2012-08-09 |
| EP2670401B1 (en) | 2015-06-10 |
| SI2670401T1 (sl) | 2015-10-30 |
| PL2670401T3 (pl) | 2015-11-30 |
| EP2670401A1 (en) | 2013-12-11 |
| BR112013019643B1 (pt) | 2022-04-19 |
| ES2543567T3 (es) | 2015-08-20 |
| US20130296357A1 (en) | 2013-11-07 |
| EA023404B1 (ru) | 2016-05-31 |
| CY1116662T1 (el) | 2017-03-15 |
| AU2012212142A1 (en) | 2013-08-15 |
| KR101521861B1 (ko) | 2015-05-21 |
| US8703787B2 (en) | 2014-04-22 |
| CN103458881A (zh) | 2013-12-18 |
| HRP20150946T1 (hr) | 2015-10-09 |
| BR112013019643A2 (pt) | 2016-10-04 |
| JP2014504646A (ja) | 2014-02-24 |
| CA2824092A1 (en) | 2012-08-09 |
| JP5837095B2 (ja) | 2015-12-24 |
| ME02200B (me) | 2016-02-20 |
| RS54189B1 (sr) | 2015-12-31 |
| AU2012212142B2 (en) | 2015-09-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2824092C (en) | Use of alk inhibitors for the treatment of eml4-alk+ non-small cell lung cancer | |
| US11478469B2 (en) | Combination product of BCL-2 inhibitor and MDM2 inhibitor and use thereof in the prevention and/or treatment of diseases | |
| TWI389893B (zh) | 二（芳胺基）芳基化合物 | |
| US20150202203A1 (en) | Method of Treating Gastrointestinal Stromal Tumors | |
| CN101137382A (zh) | 含有杂环化合物作为活性成分的免疫抑制剂和抗肿瘤剂 | |
| ES2930106T3 (es) | Compuesto derivado de pirrol-piridina, procedimiento para preparar el mismo y composición farmacéutica que contiene el mismo como ingrediente activo para la prevención o el tratamiento de enfermedades relacionadas con la proteína quinasa | |
| KR20190110581A (ko) | 암 치료 | |
| US20180303817A1 (en) | Therapeutic agent for breast cancer | |
| KR20230154793A (ko) | 암 치료를 위한 병용 요법 | |
| AU2019241625A1 (en) | Therapeutic agent for hepatocellular carcinoma | |
| KR20210126654A (ko) | 암 치료 | |
| US20240197737A1 (en) | Application of compound in preparation of inhibitory drug targeting erbb2 mutant | |
| KR102505218B1 (ko) | BCL-2 억제제와 MCl-1 억제제의 조합물, 이의 용도 및 약학적 조성물 | |
| EP2177222B1 (en) | Pyrimidylaminobenzamide derivatives for the treatment of neurofibromatosis | |
| CN103638028A (zh) | 嘧啶基氨基苯甲酰胺衍生物用于治疗全身性肥大细胞增多症的应用 | |
| CN113840823B (zh) | 显示癌细胞生长抑制效果的新型杂环取代的嘧啶衍生物，以及包含其的药物组合物 | |
| WO2017090699A1 (ja) | ピラジンカルボキサミド化合物を有効成分とするがん免疫治療用医薬組成物、及び／又は、免疫活性化用医薬組成物 | |
| TW202140005A (zh) | 用於治療發炎疾病之新穎藥物 | |
| US20250339412A1 (en) | Methods of treating solid tumor using (19r)-5-chloro-3-ethyl-16-fluoro-10,19-dimethyl-20-oxa-3,4,10,11,23-pentaazapentacyclo[19.3.1.02,6.08,12.013,18]pentacosa-1(24),2(6),4,8,11,13,15,17,21(25),22-decaen-22-amine | |
| CN110664811A (zh) | 阿法替尼在抗结核分枝杆菌药物中的应用 | |
| Jasim et al. | A comprehensive review of immunotherapy in gastrointestinal tumors with a focus on the role of combination therapy with PARP inhibitors | |
| CN115040519A (zh) | Egfr抑制剂用于治疗非常见或非经典突变的用途 | |
| HK40007956A (en) | Combination of a bcl-2 inhibitor and a mcl-1 inhibitor, uses and pharmaceutical compositions thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20170123 |