SG11201908531WA - Combination therapies for the treatment of breast cancer - Google Patents
Combination therapies for the treatment of breast cancerInfo
- Publication number
- SG11201908531WA SG11201908531WA SG11201908531WA SG11201908531WA SG 11201908531W A SG11201908531W A SG 11201908531WA SG 11201908531W A SG11201908531W A SG 11201908531WA SG 11201908531W A SG11201908531W A SG 11201908531WA
- Authority
- SG
- Singapore
- Prior art keywords
- international
- massachusetts
- rule
- pct
- applicant
- Prior art date
Links
Classifications
-
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non 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
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/453—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with oxygen as a 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
- A61K31/495—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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
-
- 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
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- 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
INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date 20 September 2018 (20.09.2018) WIP0 I PCT o mono VIII °nolo mo IIIII Ho oimIE (10) International Publication Number WO 2018/170447 Al (51) International Patent Classification: A61K 45/06 (2006.01) A61K 31/519 (2006.01) A61K 31/445 (2006.01) A61P 35/00 (2006.01) (21) International Application Number: PCT/US2018/022961 Declarations under Rule 4.17: as to applicant's entitlement to apply for and be granted a patent (Rule 4.17(ii)) as to the applicant's entitlement to claim the priority of the earlier application (Rule 4.17(iii)) W O 20 18/ 17 0 447 Al (22) International Filing Date: Published: 16 March 2018 (16.03.2018) — with international search report (Art. 21(3)) (25) Filing Language: English with sequence listing part of description (Rule 5.2(a)) (26) Publication Language: English (30) Priority Data: 62/472,345 16 March 2017 (16.03.2017) US (71) Applicant: EISAI R&D MANAGEMENT CO., LTD. [JP/JP]; 6-10 Koishikawa, 4-Chome, Bunkyo-ku, Tokyo, 112-8088 (JP). (72) Inventors; and (71) Applicants (for US only): KARR, Craig D. [US/US]; 550 Liberty Street, Braintree, Massachusetts 02184 (US). KO- RPAL, Manav [CA/US]; 18 Myrtle Street, Winchester, Massachusetts 01890 (US). RIOUX, Nathalie [CA/US]; 5 Highview Road, Woburn, Massachusetts 01801 (US). SMITH, Peter Gerard [GB/US]; 173A Franklin Street, Arlington, Massachusetts 02474 (US). (74) Agent: WALTERS, Todd R. et al.; Buchanan Inger- soll & Rooney PC, P.O. Box 1404, Alexandria, Virginia 22313-1404 (US). (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, JO, 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). (54) Title: COMBINATION THERAPIES FOR THE TREATMENT OF BREAST CANCER (57) : Provided herein is a combination therapy useful for the treatment breast cancer. The combination comprises an ER- alpha inhibitor and a CDK 4/6 inhibitor.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201762472345P | 2017-03-16 | 2017-03-16 | |
PCT/US2018/022961 WO2018170447A1 (en) | 2017-03-16 | 2018-03-16 | Combination therapies for the treatment of breast cancer |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11201908531WA true SG11201908531WA (en) | 2019-10-30 |
Family
ID=61874039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201908531W SG11201908531WA (en) | 2017-03-16 | 2018-03-16 | Combination therapies for the treatment of breast cancer |
Country Status (14)
Country | Link |
---|---|
US (1) | US11083722B2 (en) |
EP (2) | EP4218820A3 (en) |
JP (1) | JP7219224B2 (en) |
KR (1) | KR102517650B1 (en) |
CN (1) | CN110636862A (en) |
AU (1) | AU2018234903B2 (en) |
BR (1) | BR112019019261A2 (en) |
CA (1) | CA3056701A1 (en) |
IL (1) | IL269357A (en) |
MA (1) | MA47776A (en) |
MX (1) | MX2019010981A (en) |
RU (1) | RU2764724C2 (en) |
SG (1) | SG11201908531WA (en) |
WO (1) | WO2018170447A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2747399C2 (en) * | 2016-11-28 | 2021-05-04 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Indazole derivative salts and their crystals |
AU2019205821A1 (en) | 2018-01-08 | 2020-07-09 | G1 Therapeutics, Inc. | G1T38 superior dosage regimes |
US20230404987A1 (en) * | 2020-11-06 | 2023-12-21 | Eisai R&D Management Co., Ltd. | Method of treating breast cancer |
CN113018357A (en) * | 2021-02-08 | 2021-06-25 | 湖南农业大学 | Application of tea polyphenol and palbociclib combination in preparation of preparation for treating breast cancer |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6399633B1 (en) | 1999-02-01 | 2002-06-04 | Aventis Pharmaceuticals Inc. | Use of 4-H-1-benzopryan-4-one derivatives as inhibitors of smooth muscle cell proliferation |
DE19959546A1 (en) | 1999-12-09 | 2001-06-21 | Rhone Poulenc Rorer Gmbh | Pharmaceutical preparation for the treatment of tumor diseases |
KR100825530B1 (en) | 2000-01-18 | 2008-04-25 | 아벤티스 파마슈티칼스 인크. | Ethanol solvate of --cis-2-2-chlorophenyl-5,7-dihydroxy-8[4?-3?-hydroxy-1-methylpiperidinyl]-4?-1-benzopyran-4-one |
SI1259507T1 (en) | 2000-01-18 | 2005-02-28 | Aventis Pharmaceuticals Inc. | Pseudopolymorph of (-)-cis-2-(2-chlorophenyl)-5,7-dihydroxy-8 4r-(3s-hydroxy-1-methyl)piperidinyl)-4h-1-benzopyran-4-one hydrochloride |
WO2002022133A1 (en) | 2000-09-12 | 2002-03-21 | Virginia Commonwealth University | Promotion of adoptosis in cancer cells by co-administration of cyclin dependent kinase inhibitors and cellular differentiation agents |
CN101001857B (en) | 2002-01-22 | 2011-06-22 | 沃尼尔·朗伯有限责任公司 | 2-(pyridin-2-ylamino)-pyrido [2,3-d]pyrimidin-7-ones |
PL1651612T3 (en) | 2003-07-22 | 2012-09-28 | Astex Therapeutics Ltd | 3,4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators |
AR054425A1 (en) | 2005-01-21 | 2007-06-27 | Astex Therapeutics Ltd | PIPERIDIN ADDITION SALTS 4-IL-ACID AMID 4- (2,6-DICLORO-BENZOILAMINO) 1H-PIRAZOL-3-CARBOXILICO. |
MX2007008781A (en) | 2005-01-21 | 2007-09-11 | Astex Therapeutics Ltd | Pharmaceutical compounds. |
JP5475234B2 (en) | 2005-01-21 | 2014-04-16 | アステックス・セラピューティクス・リミテッド | Pharmaceutical compounds |
RU2007131101A (en) | 2005-01-21 | 2009-02-27 | Астекс Терапьютикс Лимитед (Gb) | COMBINATIONS OF PYRAZOLIC KINASE INHIBITORS AND OTHER MEDICINES AGAINST MALIGNANT NEW FORMATIONS |
JP2008255008A (en) | 2005-07-19 | 2008-10-23 | Tokyo Medical & Dental Univ | Synoviocyte proliferation inhibitor |
US7776832B2 (en) * | 2006-04-21 | 2010-08-17 | Gem Pharmaceuticals, Llc | Anticancer treatment with a combination of taxanes and 13-deoxyanthracyclines |
JO3235B1 (en) | 2006-05-26 | 2018-03-08 | Astex Therapeutics Ltd | Pyrrolopyrimidine compounds and their uses |
JP2009542608A (en) | 2006-06-29 | 2009-12-03 | アステックス・セラピューティクス・リミテッド | Pharmaceutical combination |
JP2009543770A (en) | 2006-07-14 | 2009-12-10 | アステックス・セラピューティクス・リミテッド | Combinations of pyrazole derivatives for the inhibition of CDK and GSK |
JP2009543768A (en) | 2006-07-14 | 2009-12-10 | アステックス・セラピューティクス・リミテッド | Pharmaceutical combination |
WO2008009954A1 (en) | 2006-07-21 | 2008-01-24 | Astex Therapeutics Limited | Medical use of cyclin dependent kinases inhibitors |
US7902147B2 (en) | 2007-11-05 | 2011-03-08 | Duke University | Chronic lymphocytic leukemia prognosis and treatment |
PT2331547E (en) | 2008-08-22 | 2014-10-29 | Novartis Ag | Pyrrolopyrimidine compounds as cdk inhibitors |
JO2885B1 (en) | 2008-12-22 | 2015-03-15 | ايلي ليلي اند كومباني | Protein kinase inhibitors |
UY33226A (en) | 2010-02-19 | 2011-09-30 | Novartis Ag | PIRROLOPIRIMIDINE COMPUTERS DEUTERATED AS INHIBITORS OF THE CDK4 / 6 |
ES2689177T3 (en) | 2010-04-13 | 2018-11-08 | Novartis Ag | Combination comprising a cyclin dependent kinase 4 inhibitor or cyclin dependent kinase (CDK4 / 6) and an mTOR inhibitor for treating cancer |
GB2483736B (en) * | 2010-09-16 | 2012-08-29 | Aragon Pharmaceuticals Inc | Estrogen receptor modulators and uses thereof |
MX367795B (en) | 2010-10-25 | 2019-09-06 | G1 Therapeutics Inc | Cdk inhibitors. |
US20120115878A1 (en) | 2010-11-10 | 2012-05-10 | John Vincent Calienni | Salt(s) of 7-cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-7h-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide and processes of making thereof |
PT2688887E (en) | 2011-03-23 | 2015-07-06 | Amgen Inc | Fused tricyclic dual inhibitors of cdk 4/6 and flt3 |
US9408847B2 (en) | 2012-11-28 | 2016-08-09 | Novartis Ag | Combination therapy |
CN105473140B (en) | 2013-03-15 | 2018-04-10 | G1治疗公司 | To the instantaneous protection of normal cell during chemotherapy |
HRP20211879T1 (en) | 2013-08-14 | 2022-03-04 | Novartis Ag | Combination therapy for the treatment of cancer |
JP2017507964A (en) | 2014-03-13 | 2017-03-23 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | Therapeutic combinations using estrogen receptor modulators |
WO2016025650A1 (en) | 2014-08-13 | 2016-02-18 | Celgene Avilomics Research, Inc. | Combinations of an erk inhibitor and a cdk4/6 inhibitor and related methods |
WO2016040848A1 (en) | 2014-09-12 | 2016-03-17 | G1 Therapeutics, Inc. | Treatment of rb-negative tumors using topoisomerase inhibitors in combination with cyclin dependent kinase 4/6 inhibitors |
CN104529904B (en) | 2015-01-09 | 2016-08-31 | 苏州明锐医药科技有限公司 | The preparation method of Bo Maxini |
WO2016126889A1 (en) | 2015-02-03 | 2016-08-11 | G1 Therapeutics, Inc. | Cdk4/6 inhibitor dosage formulations for the protection of hematopoietic stem and progenitor cells during chemotherapy |
IL255148B2 (en) * | 2015-04-29 | 2023-04-01 | Radius Pharmaceuticals Inc | Rad 1901 for use in a method of inhibiting tumor growth or producing tumor regression in a subject having a drug-resistant and/or mutant estrogen receptor alpha-positive cancer |
DK3302471T3 (en) | 2015-05-29 | 2021-11-15 | Eisai R&D Man Co Ltd | TETRA-SUBSTITUTED ALKENE COMPOUNDS AND THEIR USE |
-
2018
- 2018-03-16 WO PCT/US2018/022961 patent/WO2018170447A1/en unknown
- 2018-03-16 MX MX2019010981A patent/MX2019010981A/en unknown
- 2018-03-16 AU AU2018234903A patent/AU2018234903B2/en active Active
- 2018-03-16 BR BR112019019261-1A patent/BR112019019261A2/en unknown
- 2018-03-16 JP JP2019550800A patent/JP7219224B2/en active Active
- 2018-03-16 CN CN201880030008.9A patent/CN110636862A/en active Pending
- 2018-03-16 RU RU2019132893A patent/RU2764724C2/en active
- 2018-03-16 EP EP23159590.1A patent/EP4218820A3/en active Pending
- 2018-03-16 CA CA3056701A patent/CA3056701A1/en active Pending
- 2018-03-16 KR KR1020197029851A patent/KR102517650B1/en active IP Right Grant
- 2018-03-16 US US16/493,931 patent/US11083722B2/en active Active
- 2018-03-16 SG SG11201908531W patent/SG11201908531WA/en unknown
- 2018-03-16 EP EP18715441.4A patent/EP3595725B1/en active Active
- 2018-03-16 MA MA047776A patent/MA47776A/en unknown
-
2019
- 2019-09-15 IL IL26935719A patent/IL269357A/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO2018170447A1 (en) | 2018-09-20 |
EP4218820A2 (en) | 2023-08-02 |
EP3595725A1 (en) | 2020-01-22 |
BR112019019261A2 (en) | 2020-06-16 |
AU2018234903A1 (en) | 2019-10-10 |
RU2019132893A (en) | 2021-04-16 |
KR102517650B1 (en) | 2023-04-05 |
JP2020510075A (en) | 2020-04-02 |
EP4218820A3 (en) | 2023-09-20 |
AU2018234903B2 (en) | 2024-02-08 |
US20210113537A1 (en) | 2021-04-22 |
CN110636862A (en) | 2019-12-31 |
RU2764724C2 (en) | 2022-01-19 |
EP3595725B1 (en) | 2023-05-03 |
IL269357A (en) | 2019-11-28 |
CA3056701A1 (en) | 2018-09-20 |
US11083722B2 (en) | 2021-08-10 |
MA47776A (en) | 2020-01-22 |
RU2019132893A3 (en) | 2021-06-24 |
JP7219224B2 (en) | 2023-02-07 |
KR20190125448A (en) | 2019-11-06 |
MX2019010981A (en) | 2020-09-07 |
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