PL2209375T3 - Związki, kompozycje i metody stosowania inhibitorów PARP - Google Patents

Związki, kompozycje i metody stosowania inhibitorów PARP

Info

Publication number
PL2209375T3
PL2209375T3 PL08836018T PL08836018T PL2209375T3 PL 2209375 T3 PL2209375 T3 PL 2209375T3 PL 08836018 T PL08836018 T PL 08836018T PL 08836018 T PL08836018 T PL 08836018T PL 2209375 T3 PL2209375 T3 PL 2209375T3
Authority
PL
Poland
Prior art keywords
compositions
methods
inhibitor compounds
parp inhibitor
parp
Prior art date
Application number
PL08836018T
Other languages
English (en)
Inventor
Weizheng Xu
Greg Delahanty
Ling Wei
Jie Zhang
Original Assignee
Eisai Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40526672&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PL2209375(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Eisai Inc filed Critical Eisai Inc
Publication of PL2209375T3 publication Critical patent/PL2209375T3/pl

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/06Peri-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
PL08836018T 2007-10-03 2008-10-02 Związki, kompozycje i metody stosowania inhibitorów PARP PL2209375T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US97711507P 2007-10-03 2007-10-03
EP08836018.5A EP2209375B1 (en) 2007-10-03 2008-10-02 Parp inhibitor compounds, compositions and methods of use
PCT/US2008/078606 WO2009046205A1 (en) 2007-10-03 2008-10-02 Parp inhibitor compounds, compositions and methods of use

Publications (1)

Publication Number Publication Date
PL2209375T3 true PL2209375T3 (pl) 2014-12-31

Family

ID=40526672

Family Applications (1)

Application Number Title Priority Date Filing Date
PL08836018T PL2209375T3 (pl) 2007-10-03 2008-10-02 Związki, kompozycje i metody stosowania inhibitorów PARP

Country Status (27)

Country Link
US (3) US8236802B2 (pl)
EP (2) EP2842956A1 (pl)
JP (1) JP5439380B2 (pl)
KR (1) KR101596526B1 (pl)
CN (1) CN102083314B (pl)
AU (1) AU2008308664B2 (pl)
BR (1) BRPI0820518B1 (pl)
CA (1) CA2700903C (pl)
CL (1) CL2010000320A1 (pl)
CY (1) CY1115747T1 (pl)
DK (1) DK2209375T3 (pl)
ES (1) ES2504690T3 (pl)
HR (1) HRP20140853T1 (pl)
IL (1) IL204776A (pl)
JO (1) JO3170B1 (pl)
MX (1) MX2010003564A (pl)
MY (1) MY155237A (pl)
NZ (1) NZ585012A (pl)
PL (1) PL2209375T3 (pl)
PT (1) PT2209375E (pl)
RU (1) RU2485122C2 (pl)
SG (1) SG185272A1 (pl)
SI (1) SI2209375T1 (pl)
TW (1) TWI426912B (pl)
UA (1) UA99483C2 (pl)
WO (1) WO2009046205A1 (pl)
ZA (1) ZA201002317B (pl)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2319847A3 (en) 2005-01-19 2012-06-20 Eisai Inc. Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting PARP
PL2209375T3 (pl) 2007-10-03 2014-12-31 Eisai Inc Związki, kompozycje i metody stosowania inhibitorów PARP
EP2767537B1 (en) * 2008-08-06 2017-04-12 Medivation Technologies, Inc. Dihydropyridophthalazinone inhibitors of poly(ADP-ribose)polymerase (PARP)
EP2322658A1 (en) 2009-11-13 2011-05-18 Centre National de la Recherche Scientifique (CNRS) Signature for the diagnosis of breast cancer aggressiveness and genetic instability
DK2533640T3 (en) * 2010-02-08 2017-01-23 Medivation Technologies Inc METHODS OF SYNTHESIS OF DIHYDROPYRIDOPHTHALAZINE DERIVATIVES
DK2582847T3 (en) 2010-06-18 2016-12-19 Myriad Genetics Inc METHODS AND MATERIALS TO ASSESS loss of heterozygosity
WO2012074840A2 (en) * 2010-11-22 2012-06-07 The General Hospital Corporation Compositions and methods for in vivo imaging
CA2865468C (en) * 2011-03-11 2021-05-04 Sarissa Inc. Methods of treating cancer by inhibition of dna repair proteins
WO2012141990A1 (en) * 2011-04-11 2012-10-18 Abb Vie Inc. Parp inhibitors for the treatment of cipn
CN103827314A (zh) 2011-05-18 2014-05-28 国家科学研究中心 用于诊断癌侵袭性和遗传不稳定性的标记
US9181266B2 (en) * 2011-07-13 2015-11-10 Novartis Ag 2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors
WO2013028495A1 (en) * 2011-08-19 2013-02-28 Biomarin Pharmaceutical Inc. Dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) for the treatment of multiple myeloma
EP2794907B2 (en) * 2011-12-21 2022-11-23 Myriad Genetics, Inc. Methods and materials for assessing loss of heterozygosity
CN104145030B (zh) 2012-01-05 2016-10-12 国家科学研究中心 用于诊断肺癌侵袭性和遗传不稳定性的标记
CN105492011A (zh) 2013-04-08 2016-04-13 丹尼斯·M·布朗 不理想给药化学化合物的治疗增效
CA2938626A1 (en) 2013-07-26 2015-01-29 John Rothman Compositions to improve the therapeutic benefit of bisantrene
CA2946538A1 (en) 2014-04-04 2015-10-08 Del Mar Pharmaceuticals Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer
US10238630B2 (en) 2014-05-28 2019-03-26 Eisai R&D Management Co., Ltd. Use of eribulin and poly (ADP ribose) polymerase (PARP) inhibitors as combination therapy for the treatment of cancer
TW201702218A (zh) 2014-12-12 2017-01-16 美國杰克森實驗室 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法
WO2016138574A1 (en) 2015-03-02 2016-09-09 Sinai Health System Homologous recombination factors
CN104945406B (zh) * 2015-05-25 2017-10-10 苏州康润医药有限公司 氮杂非那烯‑3‑酮的衍生物、其制备方法及其作为parp抑制剂的应用
ES2879434T3 (es) 2015-07-23 2021-11-22 Inst Curie Uso de una combinación de molécula Dbait e inhibidores de PARP para tratamiento del cáncer
WO2018162439A1 (en) 2017-03-08 2018-09-13 Onxeo New predictive biomarker for the sensitivity to a treatment of cancer with a dbait molecule
WO2018165615A1 (en) * 2017-03-09 2018-09-13 The Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Parp-1 and methods of use thereof
US12121518B2 (en) * 2017-03-09 2024-10-22 The Board Of Supervisors Of Louisiana State Universi And Agricultural And Mechanical College PARP-1 and methods of use thereof
IL322309A (en) 2017-05-24 2025-09-01 Novartis Ag IL2 antibody grafted proteins and methods of use in cancer treatment
US20200407720A1 (en) 2018-03-13 2020-12-31 Onxeo A dbait molecule against acquired resistance in the treatment of cancer
MA54091A (fr) 2018-10-30 2021-09-15 Repare Therapeutics Inc Composés, compositions pharmaceutiques, procédés de préparation de composés et leur utilisation en tant qu'inhibiteurs de kinase atr
CN114502549B (zh) * 2019-10-10 2024-10-25 埃斯特韦制药股份公司 针对疼痛具有多模态活性的高哌嗪基和高哌啶基喹唑啉-4(3h)-酮衍生物
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
WO2021249996A1 (en) 2020-06-08 2021-12-16 Oncology Venture ApS Compositions comprising 2x-121 and methods for treating coronavirus infection
CN114053276B (zh) * 2020-07-30 2024-05-07 江苏天士力帝益药业有限公司 一种parp抑制剂tsl-1502中间体tsl-1502m的用途
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
CN121398822A (zh) 2023-06-21 2026-01-23 四方生物科学有限公司 用于在治疗hr功能正常的癌症的方法中的用途的包含脱氧胞苷衍生物和parp抑制剂的组合
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
TW202530228A (zh) 2023-10-12 2025-08-01 美商銳新醫藥公司 Ras抑制劑
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025217307A1 (en) 2024-04-09 2025-10-16 Revolution Medicines, Inc. Methods for predicting response to a ras(on) inhibitor and combination therapies
TW202547461A (zh) 2024-05-17 2025-12-16 美商銳新醫藥公司 Ras抑制劑
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5215738A (en) 1985-05-03 1993-06-01 Sri International Benzamide and nicotinamide radiosensitizers
US5032617A (en) 1985-05-03 1991-07-16 Sri International Substituted benzamide radiosensitizers
US5041653A (en) 1985-05-03 1991-08-20 Sri International Substituted benzamide radiosensitizers
US5177075A (en) 1988-08-19 1993-01-05 Warner-Lambert Company Substituted dihydroisoquinolinones and related compounds as potentiators of the lethal effects of radiation and certain chemotherapeutic agents; selected compounds, analogs and process
GB9702701D0 (en) 1997-02-01 1997-04-02 Univ Newcastle Ventures Ltd Quinazolinone compounds
US20020028813A1 (en) 1997-09-03 2002-03-07 Paul F. Jackson Thioalkyl compounds, methods, and compositions for inhibiting parp activity
WO1999011622A1 (en) 1997-09-03 1999-03-11 Guilford Pharmaceuticals Inc. Amino-substituted compounds, methods, and compositions for inhibiting parp activity
WO1999011644A1 (en) 1997-09-03 1999-03-11 Guilford Pharmaceuticals Inc. Di-n-heterocyclic compounds, methods, and compositions for inhibiting parp activity
US6635642B1 (en) 1997-09-03 2003-10-21 Guilford Pharmaceuticals Inc. PARP inhibitors, pharmaceutical compositions comprising same, and methods of using same
US6197785B1 (en) 1997-09-03 2001-03-06 Guilford Pharmaceuticals Inc. Alkoxy-substituted compounds, methods, and compositions for inhibiting PARP activity
US5950784A (en) 1997-09-03 1999-09-14 Yang; Shu-Chiung C. Hub structural improvement
US6291425B1 (en) 1999-09-01 2001-09-18 Guilford Pharmaceuticals Inc. Compounds, methods and pharmaceutical compositions for treating cellular damage, such as neural or cardiovascular tissue damage
AU9297998A (en) 1998-05-15 1999-12-06 Guilford Pharmaceuticals Inc. Carboxamide compounds, compositions, and methods for inhibiting parp activity
WO1999059975A1 (en) 1998-05-15 1999-11-25 Guilford Pharmaceuticals Inc. Fused tricyclic compounds which inhibit parp activity
US6387902B1 (en) 1998-12-31 2002-05-14 Guilford Pharmaceuticals, Inc. Phenazine compounds, methods and pharmaceutical compositions for inhibiting PARP
US6201020B1 (en) 1998-12-31 2001-03-13 Guilford Pharmaceuticals, Inc. Ortho-diphenol compounds, methods and pharmaceutical compositions for inhibiting parp
HRP20010573B1 (en) 1999-01-11 2006-04-30 Agouron Pharmaceuticals Tricyclic inhibitors of poly(adp-ribose) polymerases
ATE372337T1 (de) 2000-02-01 2007-09-15 Abbott Gmbh & Co Kg Heterozyklische verbindungen und deren anwendung als parp-inhibitoren
US7122679B2 (en) 2000-05-09 2006-10-17 Cephalon, Inc. Multicyclic compounds and the use thereof
DE10022925A1 (de) 2000-05-11 2001-11-15 Basf Ag Substituierte Indole als PARP-Inhibitoren
US7449464B2 (en) 2003-03-12 2008-11-11 Kudos Pharmaceuticals Limited Phthalazinone derivatives
BRPI0408284B8 (pt) * 2003-03-12 2021-05-25 Kudos Pharm Ltd compostos derivados de ftalazinona, seu uso e composição farmacêutica compreendendo os mesmos
ES2396334T3 (es) * 2003-05-28 2013-02-20 Eisai Inc. Compuestos, métodos y composiciones farmacéuticas para la inhibición de PARP
CA2527832A1 (en) * 2003-06-10 2004-12-23 F. Hoffmann-La Roche Ag 1.3.4-triaza-phenalene and 1,3,4,6-tetraazaphenalene derivatives
ATE454893T1 (de) 2003-07-25 2010-01-15 Cancer Rec Tech Ltd Tricyclische parp-hemmer
GB0317466D0 (en) 2003-07-25 2003-08-27 Univ Sheffield Use
WO2005053662A1 (en) 2003-12-01 2005-06-16 Kudos Pharmaceuticals Limited Dna damage repair inhibitors for treatment of cancer
WO2006013060A1 (en) 2004-08-04 2006-02-09 Phosphonics Ltd Substituted organopolysiloxanes and use thereof
EP2319847A3 (en) * 2005-01-19 2012-06-20 Eisai Inc. Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting PARP
PL2209375T3 (pl) 2007-10-03 2014-12-31 Eisai Inc Związki, kompozycje i metody stosowania inhibitorów PARP
WO2009137411A1 (en) 2008-05-09 2009-11-12 Allergan, Inc. Therapeutic compounds
JP2013531007A (ja) 2010-07-08 2013-08-01 ワイス・エルエルシー 皮膚障害の治療に有用な新規キノリンエステル

Also Published As

Publication number Publication date
CN102083314A (zh) 2011-06-01
UA99483C2 (ru) 2012-08-27
JO3170B1 (ar) 2017-09-20
KR101596526B1 (ko) 2016-02-22
HK1146792A1 (en) 2011-07-15
NZ585012A (en) 2012-06-29
DK2209375T3 (da) 2014-10-06
MX2010003564A (es) 2010-09-10
AU2008308664A1 (en) 2009-04-09
US8894989B2 (en) 2014-11-25
AU2008308664B2 (en) 2014-07-17
EP2209375A4 (en) 2011-03-09
US8236802B2 (en) 2012-08-07
CA2700903A1 (en) 2009-04-09
IL204776A (en) 2015-09-24
EP2209375A1 (en) 2010-07-28
CL2010000320A1 (es) 2011-03-11
TWI426912B (zh) 2014-02-21
PT2209375E (pt) 2014-10-08
RU2485122C2 (ru) 2013-06-20
KR20100100771A (ko) 2010-09-15
BRPI0820518B1 (pt) 2021-09-28
TW200932239A (en) 2009-08-01
CA2700903C (en) 2017-05-30
JP5439380B2 (ja) 2014-03-12
WO2009046205A1 (en) 2009-04-09
US20090098084A1 (en) 2009-04-16
ZA201002317B (en) 2013-09-25
RU2010117397A (ru) 2011-11-10
IL204776A0 (en) 2010-11-30
CY1115747T1 (el) 2017-01-25
CN102083314B (zh) 2014-04-30
ES2504690T3 (es) 2014-10-08
EP2842956A1 (en) 2015-03-04
US20130011365A1 (en) 2013-01-10
US20150141429A1 (en) 2015-05-21
SI2209375T1 (sl) 2014-12-31
EP2209375B1 (en) 2014-08-27
BRPI0820518A2 (pt) 2020-01-14
MY155237A (en) 2015-09-30
SG185272A1 (en) 2012-11-29
JP2010540655A (ja) 2010-12-24
HRP20140853T1 (hr) 2014-10-24

Similar Documents

Publication Publication Date Title
ZA201002317B (en) Parp inhibitor compounds,compositions and methods of use
HUS1900009I1 (hu) Új vegyületek és készítmények, továbbá alkalmazási eljárásaik
IL210462A0 (en) Pyrimidine compounds, compositions and methods of use
IL196956A0 (en) Aza-benzofuranyl compounds and methods of use
IL184303A0 (en) Amino-pyridines as inhibitors of ??-secretase
PT2397142T (pt) Utilizações de inibidores da dpp iv
IL205142A0 (en) Pyridazinone derivatives as parp inhibitors
ZA200909152B (en) Triazolopyridine compounds and their use as ask inhibitors
IL197060A0 (en) Aza-benzothiophenyl compounds and methods of use
IL197869A0 (en) Compositions of chk1 inhibitors
ZA200802585B (en) Pyridopyrimidinone inhibitors of Pl3Kα
IL190292A0 (en) PYRIDOPYRIMIDINONE INHIBITORS OF P13Ka
ZA201104463B (en) Compounds and methods of use
EP2211854A4 (en) METHODS AND COMPOSITIONS FOR THE TREATMENT OF CANCER USING BENZOPYRONE-TYPE PARP INHIBITORS
HRP20160902T1 (hr) Pripravci i postupci uporabe forbolskih estera
IL208483A0 (en) Limk2 inhibitors, compositions comprising them, and methods of their use
ZA200808017B (en) Tetrahydropyridothienopyrimidine compounds and methods of use thereof
IL200387A0 (en) Heterocylic compounds, compositions comprising them and methods of their use
ZA201000992B (en) Anti-viral compounds, compositions, and methods of use
GB0621607D0 (en) Inhibitors of c-Met
IL205299A0 (en) Parp inhibitor compounds
ZA200900896B (en) Aza-benzofuranyl compounds and methods of use
ZA200901009B (en) Aza-benzothiophenyl compounds and methods of use
TH0801005083A (th) สารประกอบ องค์ประกอบ และกรรมวิธีการใช้ตัวยับยั้ง parp
GB0805693D0 (en) Combinations of P13-delta and P13-gamma kinase inhibitor compounds