SI2694072T2 - Kombinacija spojine, ki zavira AKT, in abiraterona za uporabo pri terapevtskem zdravljenju - Google Patents
Kombinacija spojine, ki zavira AKT, in abiraterona za uporabo pri terapevtskem zdravljenjuInfo
- Publication number
- SI2694072T2 SI2694072T2 SI201231202T SI201231202T SI2694072T2 SI 2694072 T2 SI2694072 T2 SI 2694072T2 SI 201231202 T SI201231202 T SI 201231202T SI 201231202 T SI201231202 T SI 201231202T SI 2694072 T2 SI2694072 T2 SI 2694072T2
- Authority
- SI
- Slovenia
- Prior art keywords
- abiraterone
- combination
- inhibitor compound
- therapeutic treatments
- akt inhibitor
- Prior art date
Links
- 229940126638 Akt inhibitor Drugs 0.000 title 1
- GZOSMCIZMLWJML-VJLLXTKPSA-N abiraterone Chemical compound C([C@H]1[C@H]2[C@@H]([C@]3(CC[C@H](O)CC3=CC2)C)CC[C@@]11C)C=C1C1=CC=CN=C1 GZOSMCIZMLWJML-VJLLXTKPSA-N 0.000 title 1
- 229960000853 abiraterone Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 239000003197 protein kinase B inhibitor Substances 0.000 title 1
- 230000001225 therapeutic effect Effects 0.000 title 1
- 238000011282 treatment Methods 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
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- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
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- A61K31/282—Platinum compounds
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
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- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/436—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
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- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/40—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against enzymes
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- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Endocrinology (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Urology & Nephrology (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Reproductive Health (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161470803P | 2011-04-01 | 2011-04-01 | |
US201161470624P | 2011-04-01 | 2011-04-01 | |
PCT/US2012/031679 WO2012135759A1 (en) | 2011-04-01 | 2012-03-30 | Combinations of akt inhibitor compounds and abiraterone, and methods of use |
EP12764765.9A EP2694072B2 (en) | 2011-04-01 | 2012-03-30 | Combination of akt inhibitor compound and abiraterone for use in therapeutic treatments |
Publications (2)
Publication Number | Publication Date |
---|---|
SI2694072T1 SI2694072T1 (sl) | 2018-03-30 |
SI2694072T2 true SI2694072T2 (sl) | 2024-10-30 |
Family
ID=46931958
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI201231202T SI2694072T2 (sl) | 2011-04-01 | 2012-03-30 | Kombinacija spojine, ki zavira AKT, in abiraterona za uporabo pri terapevtskem zdravljenju |
Country Status (28)
Country | Link |
---|---|
US (7) | US20150064171A1 (sl) |
EP (4) | EP2694070A4 (sl) |
JP (4) | JP6239497B2 (sl) |
KR (4) | KR101950044B1 (sl) |
CN (8) | CN112915092A (sl) |
AU (4) | AU2012236166A1 (sl) |
BR (4) | BR112013025386B1 (sl) |
CA (4) | CA2844699C (sl) |
DK (1) | DK2694072T4 (sl) |
ES (3) | ES2620644T3 (sl) |
FI (1) | FI2694072T4 (sl) |
HK (2) | HK1199244A1 (sl) |
HR (1) | HRP20180223T4 (sl) |
HU (1) | HUE036513T2 (sl) |
IL (4) | IL228641A0 (sl) |
LT (1) | LT2694072T (sl) |
ME (1) | ME02998B (sl) |
MX (4) | MX354509B (sl) |
MY (1) | MY179607A (sl) |
PL (2) | PL2694072T3 (sl) |
PT (1) | PT2694072T (sl) |
RS (1) | RS56759B2 (sl) |
RU (4) | RU2631240C2 (sl) |
SG (5) | SG10201504303SA (sl) |
SI (1) | SI2694072T2 (sl) |
TR (1) | TR201802093T4 (sl) |
WO (4) | WO2012135759A1 (sl) |
ZA (4) | ZA201308064B (sl) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
MY172151A (en) | 2008-01-04 | 2019-11-14 | Intellikine Llc | Certain chemical entities, compositions and methods |
KR20160079934A (ko) | 2008-06-16 | 2016-07-06 | 유니버시티 오브 테네시 리서치 파운데이션 | 암 치료용 화합물 |
US9447049B2 (en) | 2010-03-01 | 2016-09-20 | University Of Tennessee Research Foundation | Compounds for treatment of cancer |
US11084811B2 (en) | 2010-03-01 | 2021-08-10 | Oncternal Therapeutics, Inc. | Compounds for treatment of cancer |
BR112013017670B1 (pt) | 2011-01-10 | 2022-07-19 | Infinity Pharmaceuticals, Inc | Processos de preparação de isoquinolinonas e formas sólidas de isoquinolinonas |
SG191724A1 (en) | 2011-01-11 | 2013-08-30 | Glaxosmithkline Llc | Combination |
SI2694072T2 (sl) | 2011-04-01 | 2024-10-30 | Genentech, Inc. | Kombinacija spojine, ki zavira AKT, in abiraterona za uporabo pri terapevtskem zdravljenju |
US9216170B2 (en) | 2012-03-19 | 2015-12-22 | Hoffmann-La Roche Inc. | Combination therapy for proliferative disorders |
US20150023954A1 (en) * | 2012-03-23 | 2015-01-22 | Memorial Sloan-Kettering Cancer Center | Potentiating antibody-induced complement-mediated cytotoxicity via pi3k inhibition |
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