SG11201806855WA - Combination therapy with sorafenib or regorafenib and a phosphoramidate prodrug of troxacitabine - Google Patents
Combination therapy with sorafenib or regorafenib and a phosphoramidate prodrug of troxacitabineInfo
- Publication number
- SG11201806855WA SG11201806855WA SG11201806855WA SG11201806855WA SG11201806855WA SG 11201806855W A SG11201806855W A SG 11201806855WA SG 11201806855W A SG11201806855W A SG 11201806855WA SG 11201806855W A SG11201806855W A SG 11201806855WA SG 11201806855W A SG11201806855W A SG 11201806855WA
- Authority
- SG
- Singapore
- Prior art keywords
- medivir
- box
- international
- huddinge
- troxacitabine
- Prior art date
Links
Classifications
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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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- 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
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/683—Diesters of a phosphorus acid with two hydroxy compounds, e.g. phosphatidylinositols
- A61K31/685—Diesters of a phosphorus acid with two hydroxy compounds, e.g. phosphatidylinositols one of the hydroxy compounds having nitrogen atoms, e.g. phosphatidylserine, lecithin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Abstract
XO H (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2017/151044 Al 8 September 2017 (08.09.2017) WIPO I PCT 111111111111110111011111111111010111110 01111111101011111111111111111111111110111111 W O 20 17 / 15 10 44 Al (51) International Patent Classification: A61K 31/513 (2006.01) A61P 35/00 (2006.01) A61K 31/4412 (2006.01) (21) International Application Number: PCT/SE2017/050186 (22) International Filing Date: 28 February 2017 (28.02.2017) (25) Filing Language: English (26) Publication Language: English (30) Priority Data: 1650274-2 2 March 2016 (02.03.2016) SE 1651204-8 8 September 2016 (08.09.2016) SE (71) Applicant: MEDIVIR AB [SE/SE]; Box 1086, 141 22 Huddinge (SE). (72) Inventors: ALBERTELLA, Mark; C/o Medivir Ab, Box 1086, 141 22 Huddinge (SE). ENEROTH, Anders; C/o Medivir AB, Box 1086, 141 22 Huddinge (SE). KLAS- SON, Bjorn; C/o Medivir AB, Box 1086, 141 22 Hud- dinge (SE). ()BERG, Fredrik; C/o Medivir AB, Box 1086, 141 22 Huddinge (SE). OHD, John; C/o Medivir AB, Box 1086, 141 22 Huddinge (SE). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). Published: — with international search report (Art. 21(3)) (54) Title: COMBINATION THERAPY WITH SORAFENIB OR REGORAFENIB AND A PHOSPHORAMIDATE PRODRUG = OF TROXACITABINE (57) : Combination therapy with sorafenib or regorafenib and a phosphoramidate prodrug of troxacitabine with the formula: where Y is C I -C straight or branched chain alkyl, X is H, halo, C s 3 -C 4 cycloalkyl or C i -C 4 alkyl and Z is H or fluoro, or a pharmaceut- ically acceptable salt thereof, shows surprising utility in the treatment of liver cancer or liver metastasis.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE1650274 | 2016-03-02 | ||
SE1651204 | 2016-09-08 | ||
PCT/SE2017/050186 WO2017151044A1 (en) | 2016-03-02 | 2017-02-28 | Combination therapy with sorafenib or regorafenib and a phosphoramidate prodrug of troxacitabine |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11201806855WA true SG11201806855WA (en) | 2018-09-27 |
Family
ID=59744330
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201806855WA SG11201806855WA (en) | 2016-03-02 | 2017-02-28 | Combination therapy with sorafenib or regorafenib and a phosphoramidate prodrug of troxacitabine |
Country Status (12)
Country | Link |
---|---|
US (2) | US10456413B2 (en) |
EP (1) | EP3423061A4 (en) |
JP (1) | JP6968080B2 (en) |
KR (1) | KR20180118745A (en) |
CN (2) | CN109069509B (en) |
AU (2) | AU2017227516B2 (en) |
BR (1) | BR112018067387A2 (en) |
CA (1) | CA3014769C (en) |
RU (1) | RU2018134336A (en) |
SG (1) | SG11201806855WA (en) |
WO (1) | WO2017151044A1 (en) |
ZA (1) | ZA201805445B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6968080B2 (en) | 2016-03-02 | 2021-11-17 | メディヴィル・アクチエボラーグ | Combination therapy with sorafenib or regorafenib and troxacitabine phosphoramidate prodrug |
WO2019149279A1 (en) * | 2018-02-02 | 2019-08-08 | 科济生物医药(上海)有限公司 | Combination of cellular immunotherapy |
KR20210130768A (en) * | 2019-02-18 | 2021-11-01 | 메디비르 아베 | Method for treating liver cancer using orally administered dioxolane nucleotides in combination with anti-PD1 or anti-PDL1 monoclonal antibody |
JP2023522325A (en) * | 2020-04-15 | 2023-05-30 | メディヴィル・アクチエボラーグ | MIV-818/lenvatinib combination therapy for liver cancer |
KR20210156389A (en) | 2020-06-17 | 2021-12-27 | 재단법인대구경북과학기술원 | Pharmaceutical composition for the prevention or treatment of inflammatory disease comprising regorafenib an active ingredient |
IT202000022636A1 (en) | 2020-09-25 | 2022-03-25 | Ente Ospedaliero Specializzato In Gastroenterologia Istituto Nazionale Di Ricovero E Cura A Caratter | “COMBINATION THERAPY OF SORAFENIB AND/OR REGORAFENIB WITH THE RECOMBINANT HUMAN PROTEOGLYCAN-4 PROTEIN FOR THE TREATMENT OF HEPATOCARCINOMA” |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
EP2298311B1 (en) | 1999-01-13 | 2012-05-09 | Bayer HealthCare LLC | w-Carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors |
US20030013660A1 (en) * | 2000-10-13 | 2003-01-16 | Shire Biochem Inc. | Dioxolane analogs for improved inter-cellular delivery |
US7235576B1 (en) | 2001-01-12 | 2007-06-26 | Bayer Pharmaceuticals Corporation | Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
CA2526617C (en) | 2003-05-20 | 2015-04-28 | Bayer Pharmaceuticals Corporation | Diaryl ureas with kinase inhibiting activity |
UA84156C2 (en) * | 2003-07-23 | 2008-09-25 | Байер Фармасьютикалс Корпорейшн | Fluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions |
CN101415409B (en) * | 2006-04-05 | 2012-12-05 | 诺瓦提斯公司 | Combinations of therapeutic agents for treating cancer |
US8728516B2 (en) * | 2009-04-30 | 2014-05-20 | Abbvie Inc. | Stabilized lipid formulation of apoptosis promoter |
CN102190616B (en) | 2010-03-18 | 2015-07-29 | 苏州泽璟生物制药有限公司 | A kind of deuterated synthesis of ω-diphenyl urea and the Method and process of production |
KR20230004871A (en) | 2012-04-13 | 2023-01-06 | 에피자임, 인코포레이티드 | Combination therapy for treating cancer |
CN103570613B (en) | 2012-07-18 | 2016-06-15 | 苏州泽璟生物制药有限公司 | The polymorphic form of deuterated ω-diphenyl urea or its salt |
AU2013296897B2 (en) | 2012-07-28 | 2015-09-17 | Beijing Findcure Biosciences Ltd. | Substituted pyrazolone compounds and methods of use |
US9872919B2 (en) * | 2012-09-19 | 2018-01-23 | The Research Foundation For The State University Of New York | Prodrugs for selective anticancer therapy |
KR20160099090A (en) * | 2013-11-27 | 2016-08-19 | 아이데닉스 파마슈티칼스 엘엘씨 | Nucleotides for the treatment of liver cancer |
EP3074399A1 (en) * | 2013-11-27 | 2016-10-05 | Idenix Pharmaceuticals LLC | 2'-dichloro and 2'-fluoro-2'-chloro nucleoside analogues for hcv infection |
PT3186244T (en) * | 2014-08-25 | 2020-05-29 | Medivir Ab | Dioxolane analogues of uridine for the treatment of cancer |
JP6968080B2 (en) | 2016-03-02 | 2021-11-17 | メディヴィル・アクチエボラーグ | Combination therapy with sorafenib or regorafenib and troxacitabine phosphoramidate prodrug |
-
2017
- 2017-02-28 JP JP2018545847A patent/JP6968080B2/en active Active
- 2017-02-28 US US16/081,383 patent/US10456413B2/en active Active
- 2017-02-28 SG SG11201806855WA patent/SG11201806855WA/en unknown
- 2017-02-28 RU RU2018134336A patent/RU2018134336A/en not_active Application Discontinuation
- 2017-02-28 CN CN201780014430.0A patent/CN109069509B/en active Active
- 2017-02-28 WO PCT/SE2017/050186 patent/WO2017151044A1/en active Application Filing
- 2017-02-28 KR KR1020187028361A patent/KR20180118745A/en not_active Application Discontinuation
- 2017-02-28 EP EP17760400.6A patent/EP3423061A4/en active Pending
- 2017-02-28 AU AU2017227516A patent/AU2017227516B2/en active Active
- 2017-02-28 CA CA3014769A patent/CA3014769C/en active Active
- 2017-02-28 BR BR112018067387A patent/BR112018067387A2/en active Search and Examination
- 2017-02-28 CN CN202010727607.5A patent/CN111956646B/en active Active
-
2018
- 2018-08-15 ZA ZA2018/05445A patent/ZA201805445B/en unknown
-
2019
- 2019-08-30 US US16/557,511 patent/US10960017B2/en active Active
-
2022
- 2022-06-01 AU AU2022203761A patent/AU2022203761A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
CN111956646A (en) | 2020-11-20 |
EP3423061A4 (en) | 2019-11-13 |
BR112018067387A2 (en) | 2019-01-02 |
US10456413B2 (en) | 2019-10-29 |
CA3014769C (en) | 2024-01-09 |
US20200009166A1 (en) | 2020-01-09 |
CN111956646B (en) | 2023-07-25 |
CA3014769A1 (en) | 2017-09-08 |
US10960017B2 (en) | 2021-03-30 |
EP3423061A1 (en) | 2019-01-09 |
AU2017227516A1 (en) | 2018-08-30 |
WO2017151044A1 (en) | 2017-09-08 |
US20190091246A1 (en) | 2019-03-28 |
JP6968080B2 (en) | 2021-11-17 |
KR20180118745A (en) | 2018-10-31 |
CN109069509A (en) | 2018-12-21 |
ZA201805445B (en) | 2019-07-31 |
CN109069509B (en) | 2020-10-16 |
RU2018134336A (en) | 2020-04-02 |
AU2017227516B2 (en) | 2022-03-03 |
AU2022203761A1 (en) | 2022-06-16 |
RU2018134336A3 (en) | 2020-05-22 |
JP2019507764A (en) | 2019-03-22 |
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