WO2015068142A3 - Compositions, process of preparation of said compositions, uses and method of management of myeloproliferative disorder - Google Patents
Compositions, process of preparation of said compositions, uses and method of management of myeloproliferative disorder Download PDFInfo
- Publication number
- WO2015068142A3 WO2015068142A3 PCT/IB2014/065924 IB2014065924W WO2015068142A3 WO 2015068142 A3 WO2015068142 A3 WO 2015068142A3 IB 2014065924 W IB2014065924 W IB 2014065924W WO 2015068142 A3 WO2015068142 A3 WO 2015068142A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- myeloproliferative disorder
- compositions
- jak2
- composition
- dominant
- Prior art date
Links
- 208000014767 Myeloproliferative disease Diseases 0.000 title abstract 5
- 201000007224 Myeloproliferative neoplasm Diseases 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 5
- 239000000203 mixture Substances 0.000 title abstract 4
- 108010019437 Janus Kinase 2 Proteins 0.000 abstract 3
- 102100033444 Tyrosine-protein kinase JAK2 Human genes 0.000 abstract 3
- 102100036009 5'-AMP-activated protein kinase catalytic subunit alpha-2 Human genes 0.000 abstract 1
- 101000783681 Homo sapiens 5'-AMP-activated protein kinase catalytic subunit alpha-2 Proteins 0.000 abstract 1
- 102000004861 Phosphoric Diester Hydrolases Human genes 0.000 abstract 1
- 108090001050 Phosphoric Diester Hydrolases Proteins 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 239000012822 autophagy inhibitor Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000035772 mutation Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 102200087780 rs77375493 Human genes 0.000 abstract 1
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
-
- 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
-
- 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
- A61K31/13—Amines
- A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
-
- 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
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/382—Heterocyclic compounds having sulfur as a ring hetero atom having six-membered rings, e.g. thioxanthenes
-
- 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
- A61K31/4353—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
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4706—4-Aminoquinolines; 8-Aminoquinolines, e.g. chloroquine, primaquine
-
- 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
- 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
- A61K31/53—Heterocyclic 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
The present disclosure relates to a pharmaceutical composition and a method to manage Myeloproliferative disorder or any associated condition, particularly, JAK2 (Janus Kinase 2) dominant (including JAK2V617F mutant) Myeloproliferative Disorder (MPD) and associated conditions. The disclosure provides composition comprising at least two components selected from a group comprising Phosphodiesterase Type 4 (PDE4) inhibitor, Autophagy inhibitor and AMPK agonist. The disclosure further relates to a process of preparing the said composition and a method of managing JAK2 dominant (including JAK2 V617F mutant) Myeloproliferative Disorder; existing alone or along with any other mutation.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN5103/CHE/2013 | 2013-11-11 | ||
IN5103CH2013 | 2013-11-11 | ||
IN4949CH2014 | 2014-10-01 | ||
IN4949/CHE/2014 | 2014-10-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2015068142A2 WO2015068142A2 (en) | 2015-05-14 |
WO2015068142A3 true WO2015068142A3 (en) | 2015-09-24 |
Family
ID=52014184
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2014/065924 WO2015068142A2 (en) | 2013-11-11 | 2014-11-10 | Compositions, process of preparation of said compositions, uses and method of management of myeloproliferative disorder |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2015068142A2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110917406A (en) * | 2019-12-06 | 2020-03-27 | 段传志 | Artificial blood vessel stent and preparation method and application thereof |
US20220305000A1 (en) * | 2021-03-23 | 2022-09-29 | Cellworks Group Inc. | Combination Comprising Chloroquine, Metformin and Statin for Management of Cancer, Composition and Methods Thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004060313A2 (en) * | 2002-12-30 | 2004-07-22 | Celgene Corporation | Fluoroalkoxy-substituted 1, 3-dihydro-isoindolyl compounds and their pharmaceutical uses |
WO2009011897A1 (en) * | 2007-07-17 | 2009-01-22 | Combinatorx, Incorporated | Combinations for the treatment of b-cell proliferative disorders |
WO2010114922A1 (en) * | 2009-03-31 | 2010-10-07 | Agios Pharmaceuticals, Inc. | Methods of treating cancer having an aberrant egfr or kras genotype |
WO2011100319A1 (en) * | 2010-02-09 | 2011-08-18 | Exelixis, Inc. | Methods of treating cancer using pyridopyrimidinone inhibitors of pi3k and mtor in combination with autophagy inhibitors |
WO2012171015A2 (en) * | 2011-06-10 | 2012-12-13 | Translational Genomics Research Institute | Therapeutic combination for cancer treatment |
US20130156865A1 (en) * | 2011-12-16 | 2013-06-20 | Chiesi Farmaceutici S.P.A. | Potentiation induced by pde4 inhibitors in the treatment of leukemia |
-
2014
- 2014-11-10 WO PCT/IB2014/065924 patent/WO2015068142A2/en active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004060313A2 (en) * | 2002-12-30 | 2004-07-22 | Celgene Corporation | Fluoroalkoxy-substituted 1, 3-dihydro-isoindolyl compounds and their pharmaceutical uses |
WO2009011897A1 (en) * | 2007-07-17 | 2009-01-22 | Combinatorx, Incorporated | Combinations for the treatment of b-cell proliferative disorders |
WO2010114922A1 (en) * | 2009-03-31 | 2010-10-07 | Agios Pharmaceuticals, Inc. | Methods of treating cancer having an aberrant egfr or kras genotype |
WO2011100319A1 (en) * | 2010-02-09 | 2011-08-18 | Exelixis, Inc. | Methods of treating cancer using pyridopyrimidinone inhibitors of pi3k and mtor in combination with autophagy inhibitors |
WO2012171015A2 (en) * | 2011-06-10 | 2012-12-13 | Translational Genomics Research Institute | Therapeutic combination for cancer treatment |
US20130156865A1 (en) * | 2011-12-16 | 2013-06-20 | Chiesi Farmaceutici S.P.A. | Potentiation induced by pde4 inhibitors in the treatment of leukemia |
Non-Patent Citations (4)
Title |
---|
CHRISTOPH MAACK ET AL: "Abstract 763: Human Cardiac Beta1-Adrenergic Receptors Are Desensitized By Receptor-Mediated Activation Of Phosphatidylinositol-3 Kinase and Phosphodiesterase-4 -- Maack et al. 116 (10016): II_146 -- Circulation", CIRCULATION 2007; 116(146), 1 January 2007 (2007-01-01), XP055162165, Retrieved from the Internet <URL:http://circ.ahajournals.org/cgi/content/meeting_abstract/116/16_MeetingAbstracts/II_146-c> [retrieved on 20150114] * |
CHRISTOPHER J. GREGG ET AL: "[beta]2-Adrenergic Receptor-Coupled Phosphoinositide 3-Kinase Constrains cAMP-Dependent Increases in Cardiac Inotropy Through Phosphodiesterase 4 Activation", ANESTHESIA & ANALGESIA, 1 August 2010 (2010-08-01), pages 1, XP055162556, ISSN: 0003-2999, DOI: 10.1213/ANE.0b013e3181ee8312 * |
E. VAKANA ET AL: "Antileukemic effects of AMPK activators on BCR-ABL-expressing cells", BLOOD, vol. 118, no. 24, 8 December 2011 (2011-12-08), pages 6399 - 6402, XP055162810, ISSN: 0006-4971, DOI: 10.1182/blood-2011-01-332783 * |
G. MOLOSTVOV ET AL: "The effects of selective cytokine inhibitory drugs (CC-10004 and CC-1088) on VEGF and IL-6 expression and apoptosis in myeloma and endothelial cell co-cultures", BRITISH JOURNAL OF HAEMATOLOGY, vol. 124, no. 3, 1 February 2004 (2004-02-01), pages 366 - 375, XP055162553, ISSN: 0007-1048, DOI: 10.1046/j.1365-2141.2003.04777.x * |
Also Published As
Publication number | Publication date |
---|---|
WO2015068142A2 (en) | 2015-05-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2015039612A8 (en) | Compound inhibiting activities of btk and/or jak3 kinases | |
WO2017108723A3 (en) | PYRAZOLO[1,5a]PYRIMIDINE DERIVATIVES AS IRAK4 MODULATORS | |
WO2012101654A3 (en) | Novel triazine compounds | |
MX2009011950A (en) | Pyrimidine derivatives and compositions as c-kit and pdgfr kinase inhibitors. | |
CL2013003051A1 (en) | Compounds derived from pyrazolo (4.3-d) pyrimidines, kinase inhibitors; pharmaceutical composition; and use for the treatment of diseases and disorders of the respiratory system | |
AU2012258977A8 (en) | Inhibitors of LRRK2 kinase activity | |
MX2009011951A (en) | Compounds and compositions as c-kit and pdgfr kinase inhibitors. | |
TN2010000131A1 (en) | Polo-like kinase inhibitors | |
MX347917B (en) | Imidazo [1, 2 - b] pyridazine - based compounds, compositions comprising them, and uses thereof. | |
WO2007117995A3 (en) | Kinase inhibitors | |
WO2015082887A3 (en) | Use of kinase inhibitors | |
WO2013153479A3 (en) | Indole and indazole compounds that activate ampk | |
MD20150122A2 (en) | Heteroaromatic compounds and their use as dopamine D1 ligands | |
WO2012096887A3 (en) | Compositions comprising enzyme-cleavable oxycodone prodrug | |
WO2012030927A3 (en) | Modified-release dosage forms of 5-ht2c agonists useful for weight management | |
NZ705578A (en) | Coated pharmaceutical composition containing regorafenib | |
MX2012009074A (en) | Pyrrolo [ 2, 3 - d] pyrimidine urea compounds as jak inhibitors. | |
WO2011116356A3 (en) | Positive allosteric modulators of group ii mglurs | |
GEP201706620B (en) | NOVEL 4-(SUBSTITUTED-AMINO)-7H-PYRROLO[2,3-d]PYRIMIDINES AS LRRK2 INHIBITORS | |
WO2014042433A3 (en) | Compounds and compositions for modulating adenosine a3 receptor activity | |
SG195085A1 (en) | Pyrazolo[3,4-d]pyrimidine compounds and their use as pde2 inhibitors and/or cyp3a4 inhibitors | |
WO2011106248A3 (en) | Trimethoxyphenyl inhibitors of tyrosine kinase | |
MX379383B (en) | Fused ring pyrimidine compound, intermediate, and preparation method, composition and use thereof | |
MX2009011952A (en) | Compounds and compositions as c-kit and pdgfr kinase inhibitors. | |
WO2014095920A8 (en) | New cyclohexyl and quinuclidinyl carbamate derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activity |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 14809119 Country of ref document: EP Kind code of ref document: A2 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 14809119 Country of ref document: EP Kind code of ref document: A2 |