JP2010501572A - 4−アミノキナゾリン誘導体およびその使用方法 - Google Patents
4−アミノキナゾリン誘導体およびその使用方法 Download PDFInfo
- Publication number
- JP2010501572A JP2010501572A JP2009525631A JP2009525631A JP2010501572A JP 2010501572 A JP2010501572 A JP 2010501572A JP 2009525631 A JP2009525631 A JP 2009525631A JP 2009525631 A JP2009525631 A JP 2009525631A JP 2010501572 A JP2010501572 A JP 2010501572A
- Authority
- JP
- Japan
- Prior art keywords
- cancer
- subject
- compound
- tumor
- mmol
- 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.)
- Pending
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83950306P | 2006-08-22 | 2006-08-22 | |
| PCT/US2007/018655 WO2008024439A2 (en) | 2006-08-22 | 2007-08-22 | 4-aminoquinazoline derivatives and methods of use thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010501572A true JP2010501572A (ja) | 2010-01-21 |
| JP2010501572A5 JP2010501572A5 (enExample) | 2010-09-30 |
Family
ID=39107412
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009525631A Pending JP2010501572A (ja) | 2006-08-22 | 2007-08-22 | 4−アミノキナゾリン誘導体およびその使用方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US20080051422A1 (enExample) |
| EP (1) | EP2054063A4 (enExample) |
| JP (1) | JP2010501572A (enExample) |
| KR (1) | KR20090042994A (enExample) |
| CN (1) | CN101594870A (enExample) |
| AU (1) | AU2007288204A1 (enExample) |
| CA (1) | CA2661223A1 (enExample) |
| MX (1) | MX2009001814A (enExample) |
| WO (1) | WO2008024439A2 (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012501328A (ja) * | 2008-09-02 | 2012-01-19 | アクチミス ファーマシューティカルズ インコーポレーテッド | Crth2アンタゴニストとしての同位体富化されたピリミジン−5−イル酢酸誘導体 |
| JP2012502038A (ja) * | 2008-09-03 | 2012-01-26 | テバ ファーマシューティカル インダストリーズ リミティド | 免疫機能の2−オキソ−1,2−ジヒドロ−キノリンモジュレーター |
| JP2013519708A (ja) * | 2010-02-19 | 2013-05-30 | ノバルティス アーゲー | Cdk4/6阻害剤としての重水素化ピロロピリミジン化合物 |
| JP2014508724A (ja) * | 2010-12-17 | 2014-04-10 | グラクソスミスクライン インテレクチュアル プロパティ リミテッド | 組合せ |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110053964A1 (en) * | 2006-08-22 | 2011-03-03 | Roger Tung | 4-aminoquinazoline derivatives and methods of use thereof |
| EP2054063A4 (en) * | 2006-08-22 | 2010-10-27 | Concert Pharmaceuticals Inc | 4-AMINOCHINAZOLINE DERIVATIVES AND METHOD FOR THEIR USE |
| JP5580592B2 (ja) * | 2006-09-11 | 2014-08-27 | キュリス,インコーポレイテッド | 亜鉛結合部分を含むキナゾリン系egfrインヒビター |
| US7547781B2 (en) | 2006-09-11 | 2009-06-16 | Curis, Inc. | Quinazoline based EGFR inhibitors containing a zinc binding moiety |
| US8119616B2 (en) | 2007-09-10 | 2012-02-21 | Curis, Inc. | Formulation of quinazoline based EGFR inhibitors containing a zinc binding moiety |
| US20090215802A1 (en) * | 2007-09-13 | 2009-08-27 | Protia, Llc | Deuterium-enriched lapatinib |
| JP5562865B2 (ja) | 2007-12-17 | 2014-07-30 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Trpv1のイミダゾロ−、オキサゾロ−、及びチアゾロピリミジン・モジュレーター |
| WO2009121042A1 (en) * | 2008-03-28 | 2009-10-01 | Concert Pharmaceuticals, Inc. | Quinazoline derivatives and methods of treatment |
| US8252805B2 (en) | 2008-05-07 | 2012-08-28 | Teva Pharmaceutical Industries Ltd. | Forms of lapatinib ditosylate and processes for preparation thereof |
| WO2010027848A2 (en) * | 2008-08-26 | 2010-03-11 | Teva Pharmaceutical Industries Ltd. | Forms of lapatinib compounds and processes for the preparation thereof |
| EP2328414B1 (en) * | 2008-08-29 | 2013-12-11 | Concert Pharmaceuticals Inc. | Substituted triazolo-pyridazine derivatives |
| CN101735200B (zh) * | 2008-11-17 | 2013-01-02 | 岑均达 | 喹唑啉类化合物 |
| US20110053968A1 (en) | 2009-06-09 | 2011-03-03 | Auspex Pharmaceuticals, Inc. | Aminopyrimidine inhibitors of tyrosine kinase |
| US8916574B2 (en) | 2009-09-28 | 2014-12-23 | Qilu Pharmaceutical Co., Ltd. | 4-(substituted anilino)-quinazoline derivatives useful as tyrosine kinase inhibitors |
| US20110195066A1 (en) * | 2010-02-05 | 2011-08-11 | Auspex Pharmaceuticals, Inc. | Quinoline inhibitors of tyrosine kinase |
| CN102453025B (zh) * | 2010-10-18 | 2014-08-13 | 齐鲁制药有限公司 | 拉帕替尼中间体晶型及其制备方法 |
| CN102321076B (zh) * | 2011-07-07 | 2013-08-21 | 中国科学技术大学 | 拉帕替尼中间体及其类似物的制备方法 |
| CN102659764A (zh) * | 2012-04-16 | 2012-09-12 | 中国科学院广州生物医药与健康研究院 | 酪氨酸激酶不可逆抑制剂及其制备方法和用途 |
| CZ2012712A3 (cs) | 2012-10-17 | 2014-04-30 | Zentiva, K.S. | Nový způsob výroby klíčového intermediátu výroby lapatinibu |
| CN102911164A (zh) * | 2012-11-07 | 2013-02-06 | 江苏金桥盐化集团利海化工有限公司 | 一种拉帕替尼关键中间体的制备方法 |
| ITVI20130003A1 (it) * | 2013-01-14 | 2014-07-14 | F I S Fabbrica Italiana Sint I S P A | Procedimento per la preparazione di lapatinib e suoi sali mediante nuovi intermedi. |
| US9024023B2 (en) | 2013-01-14 | 2015-05-05 | F.I.S.—Fabbrica Italiana Sintetici S.p.A. | Efficient process for the preparation of lapatinib and salts thereof by means of new intermediates |
| CN104513231A (zh) * | 2015-01-09 | 2015-04-15 | 安润医药科技(苏州)有限公司 | 拉帕替尼及其中间体的合成方法 |
| GB201611580D0 (en) * | 2016-07-01 | 2016-08-17 | Aslan Pharmaceuticals Pte Ltd | Method |
| JP2020536855A (ja) * | 2017-09-26 | 2020-12-17 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | がんを治療するための組成物及び方法 |
| CN107827877B (zh) * | 2017-11-21 | 2021-05-07 | 陕西师范大学 | 二烷基氨基喹唑啉类化合物及其在制备抗肿瘤药物中的应用 |
| CN108285421A (zh) * | 2018-01-26 | 2018-07-17 | 黑龙江鑫创生物科技开发有限公司 | 一种微通道反应器合成拉帕替尼中间体的方法 |
| CN108187055B (zh) * | 2018-03-06 | 2019-12-27 | 北京大学 | 一种具有协同增效作用的抗癌组合物 |
| CN108690001A (zh) * | 2018-06-26 | 2018-10-23 | 苏州市贝克生物科技有限公司 | 拉帕替尼类似物的合成 |
| KR20250005041A (ko) | 2021-09-23 | 2025-01-09 | 에라스카, 아이엔씨. | Egfr 억제제 다형체 형태 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005120504A2 (en) * | 2004-06-03 | 2005-12-22 | Smithkline Beecham (Cork) Limited | Cancer treatment method |
| WO2006002422A2 (en) * | 2004-06-24 | 2006-01-05 | Novartis Vaccines And Diagnostics Inc. | Compounds for immunopotentiation |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6221335B1 (en) * | 1994-03-25 | 2001-04-24 | Isotechnika, Inc. | Method of using deuterated calcium channel blockers |
| JP4386967B2 (ja) * | 1996-07-13 | 2009-12-16 | グラクソ、グループ、リミテッド | プロテインチロシンキナーゼ阻害剤としての縮合複素環式化合物 |
| US6225318B1 (en) * | 1996-10-17 | 2001-05-01 | Pfizer Inc | 4-aminoquinazolone derivatives |
| GB9800569D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| US6440710B1 (en) * | 1998-12-10 | 2002-08-27 | The Scripps Research Institute | Antibody-catalyzed deuteration, tritiation, dedeuteration or detritiation of carbonyl compounds |
| EP1104760B1 (en) * | 1999-12-03 | 2003-03-12 | Pfizer Products Inc. | Sulfamoylheteroaryl pyrazole compounds as anti-inflammatory/analgesic agents |
| TW200413273A (en) * | 2002-11-15 | 2004-08-01 | Wako Pure Chem Ind Ltd | Heavy hydrogenation method of heterocyclic rings |
| JP2007501809A (ja) * | 2003-08-08 | 2007-02-01 | ユリシーズ・ファーマシューティカル・プロダクツ・インコーポレイテッド | 抗菌剤としてのハロゲン化キナゾリニルニトロフラン |
| EP1682123A1 (en) * | 2003-11-07 | 2006-07-26 | SmithKline Beecham (Cork) Limited | Cancer treatment method |
| WO2005120512A2 (en) * | 2004-06-04 | 2005-12-22 | Smithkline Beecham (Cork) Limited | Cancer treatment method |
| CA2624179A1 (en) * | 2005-10-06 | 2007-04-12 | Auspex Pharmaceuticals, Inc. | Deuterated inhibitors of gastric h+, k+-atpase with enhanced therapeutic properties |
| US7750168B2 (en) * | 2006-02-10 | 2010-07-06 | Sigma-Aldrich Co. | Stabilized deuteroborane-tetrahydrofuran complex |
| US20110053964A1 (en) * | 2006-08-22 | 2011-03-03 | Roger Tung | 4-aminoquinazoline derivatives and methods of use thereof |
| EP2054063A4 (en) * | 2006-08-22 | 2010-10-27 | Concert Pharmaceuticals Inc | 4-AMINOCHINAZOLINE DERIVATIVES AND METHOD FOR THEIR USE |
| WO2008030382A1 (en) * | 2006-09-05 | 2008-03-13 | Schering Corporation | Pharmaceutical combinations for lipid management and in the treatment of atherosclerosis and hepatic steatosis |
| US20090215802A1 (en) * | 2007-09-13 | 2009-08-27 | Protia, Llc | Deuterium-enriched lapatinib |
| WO2010005585A2 (en) * | 2008-07-09 | 2010-01-14 | Concert Pharmaceuticals Inc. | 4-aminoquinazoline prodrugs |
-
2007
- 2007-08-22 EP EP07811504A patent/EP2054063A4/en not_active Withdrawn
- 2007-08-22 CA CA002661223A patent/CA2661223A1/en not_active Abandoned
- 2007-08-22 KR KR1020097005957A patent/KR20090042994A/ko not_active Ceased
- 2007-08-22 CN CNA2007800393013A patent/CN101594870A/zh active Pending
- 2007-08-22 US US11/895,174 patent/US20080051422A1/en not_active Abandoned
- 2007-08-22 AU AU2007288204A patent/AU2007288204A1/en not_active Abandoned
- 2007-08-22 MX MX2009001814A patent/MX2009001814A/es active IP Right Grant
- 2007-08-22 WO PCT/US2007/018655 patent/WO2008024439A2/en not_active Ceased
- 2007-08-22 JP JP2009525631A patent/JP2010501572A/ja active Pending
-
2010
- 2010-09-02 US US12/874,981 patent/US20110097320A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005120504A2 (en) * | 2004-06-03 | 2005-12-22 | Smithkline Beecham (Cork) Limited | Cancer treatment method |
| WO2006002422A2 (en) * | 2004-06-24 | 2006-01-05 | Novartis Vaccines And Diagnostics Inc. | Compounds for immunopotentiation |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012501328A (ja) * | 2008-09-02 | 2012-01-19 | アクチミス ファーマシューティカルズ インコーポレーテッド | Crth2アンタゴニストとしての同位体富化されたピリミジン−5−イル酢酸誘導体 |
| JP2012502038A (ja) * | 2008-09-03 | 2012-01-26 | テバ ファーマシューティカル インダストリーズ リミティド | 免疫機能の2−オキソ−1,2−ジヒドロ−キノリンモジュレーター |
| JP2015007060A (ja) * | 2008-09-03 | 2015-01-15 | テバ ファーマシューティカル インダストリーズ リミティド | 免疫機能の2−オキソ−1,2−ジヒドロ−キノリンモジュレーター |
| JP2013519708A (ja) * | 2010-02-19 | 2013-05-30 | ノバルティス アーゲー | Cdk4/6阻害剤としての重水素化ピロロピリミジン化合物 |
| JP2014508724A (ja) * | 2010-12-17 | 2014-04-10 | グラクソスミスクライン インテレクチュアル プロパティ リミテッド | 組合せ |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2007288204A1 (en) | 2008-02-28 |
| CA2661223A1 (en) | 2008-02-28 |
| CN101594870A (zh) | 2009-12-02 |
| KR20090042994A (ko) | 2009-05-04 |
| EP2054063A4 (en) | 2010-10-27 |
| WO2008024439A2 (en) | 2008-02-28 |
| MX2009001814A (es) | 2009-03-02 |
| US20080051422A1 (en) | 2008-02-28 |
| EP2054063A2 (en) | 2009-05-06 |
| WO2008024439A3 (en) | 2009-02-26 |
| US20110097320A1 (en) | 2011-04-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2010501572A (ja) | 4−アミノキナゾリン誘導体およびその使用方法 | |
| JP6592071B2 (ja) | ヒトezh2の阻害剤およびその使用方法 | |
| JP6779793B2 (ja) | リンパ腫を治療するためのezh2阻害剤 | |
| JP6016284B2 (ja) | ジスピロピロリジン誘導体の結晶 | |
| KR102117982B1 (ko) | 암 치료용 병용 요법 | |
| TWI623533B (zh) | 作為檢測點激酶1 (chk1)抑制劑之3,5-二取代吡唑及其製備及應用 | |
| JP5389028B2 (ja) | 置換オキサゾリジノン誘導体 | |
| KR102374933B1 (ko) | c-Met 억제제의 결정형과 이의 염 형태 및 제조 방법 | |
| US20110053964A1 (en) | 4-aminoquinazoline derivatives and methods of use thereof | |
| KR20170045350A (ko) | 형질감염 중 재배열 (ret) 키나제 억제제로서의 피리돈 유도체 | |
| RU2556205C2 (ru) | Очищенные пирролохинолинил-пирролидин-2,5-дионовые композиции и способы их получения и применения | |
| TW201036948A (en) | Malate salts of N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide, and crystalline forms thereof | |
| US8609673B2 (en) | Vandetanib derivatives | |
| TW201249835A (en) | Alkyne substituted quinazoline compounds and methods of use | |
| US8084464B2 (en) | Tetrahydroisoquinoline derivatives | |
| EP3865487A1 (en) | Aromatic ring-linked dioxane-quinazoline or -quinoline compounds, compositions and use thereof | |
| US20110129549A1 (en) | Tricyclic benzo[5,6]cyclohepta[1,2-b]pyridine derivatives and uses thereof | |
| US20240016795A1 (en) | Bromodomain inhibitors for androgen receptor-driven cancers | |
| US9107922B2 (en) | Pyrimidinecarboxamide derivatives | |
| CA2906396A1 (en) | Inhibitors of the enzyme udp-glucose: n-acyl-sphingosine glucosyltransferase | |
| EP4596553A1 (en) | Salt of dioxane quinoline compound, crystal form thereof, preparation methods therefor and uses thereof | |
| HK40057704A (en) | Aromatic ring-linked dioxane-quinazoline or -quinoline compounds, compositions and use thereof | |
| HK1257988B (en) | 3,5-disubstituted pyrazoles useful as checkpoint kinase 1 (chk1) inhibitors, and their preparations and applications |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100810 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20100810 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20121218 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130311 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130318 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130408 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130415 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130509 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130516 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130613 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20130617 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20130903 |