WO2017211937A1 - Flt3 receptor inhibitor at low dosage for the treatment of neuropathic pain - Google Patents
Flt3 receptor inhibitor at low dosage for the treatment of neuropathic pain Download PDFInfo
- Publication number
- WO2017211937A1 WO2017211937A1 PCT/EP2017/063935 EP2017063935W WO2017211937A1 WO 2017211937 A1 WO2017211937 A1 WO 2017211937A1 EP 2017063935 W EP2017063935 W EP 2017063935W WO 2017211937 A1 WO2017211937 A1 WO 2017211937A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- receptor inhibitor
- flt3 receptor
- pain
- neuropathic
- treatment
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- 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
- A61K31/495—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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the allometric FDA factor for the rat is 6.2 and the allometric FDA factor for the mouse is 12.3.
- the HED are typically calculated as the daily dose for a human with a body weight of 60 kg.
- the active daily dosage per human adult of the said FLT3 receptor inhibitor used for the treatment of any type of cancer as used in method 1 is the highest known active daily dosage when various active dosages are known for different cancers.
- Said approach may be applied to sunitinib.
- EXAMPLE 2 Effects of sunitinib on capsaicin-induced increase of extracellular calcium in Dorsal Root Ganglia (DRG)
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Nutrition Science (AREA)
- Dermatology (AREA)
- Physiology (AREA)
- Anesthesiology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2018563716A JP7134097B2 (ja) | 2016-06-08 | 2017-06-08 | 神経障害性疼痛の治療のための低用量flt3受容体阻害剤 |
| US16/307,968 US10709687B2 (en) | 2016-06-08 | 2017-06-08 | FLT3 receptor inhibitor at low dosage for the treatment of neuropathic pain |
| EP17727913.0A EP3468602B1 (en) | 2016-06-08 | 2017-06-08 | Flt3 receptor inhibitor at low dosage for the treatment of neuropathic pain |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16305669.0A EP3254698A1 (en) | 2016-06-08 | 2016-06-08 | Flt3 receptor inhibitor at low dosage for the treatment of neuropathic pain |
| EP16305669.0 | 2016-06-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2017211937A1 true WO2017211937A1 (en) | 2017-12-14 |
Family
ID=56134285
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2017/063935 Ceased WO2017211937A1 (en) | 2016-06-08 | 2017-06-08 | Flt3 receptor inhibitor at low dosage for the treatment of neuropathic pain |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US10709687B2 (https=) |
| EP (2) | EP3254698A1 (https=) |
| JP (1) | JP7134097B2 (https=) |
| HU (1) | HUE062092T2 (https=) |
| WO (1) | WO2017211937A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12441707B2 (en) | 2019-12-30 | 2025-10-14 | Tyra Biosciences, Inc. | Indazole compounds |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20220202820A1 (en) * | 2019-04-16 | 2022-06-30 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Use of jak inhibitors for the treatment of painful conditions involving nav1.7 channels |
| KR102231446B1 (ko) * | 2021-01-21 | 2021-03-24 | (주) 와이디생명과학 | 베타아밀로이드 및 타우 단백질 집적과 연관된 질환 치료용 약학적 조성물 |
| TW202340177A (zh) | 2021-12-30 | 2023-10-16 | 美商拜歐米富士恩股份有限公司 | 作為 flt3抑制劑之吡嗪化合物 |
Citations (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002032861A2 (en) | 2000-10-17 | 2002-04-25 | Merck & Co., Inc. | Orally active salts with tyrosine kinase activity |
| WO2002092599A1 (en) | 2001-05-14 | 2002-11-21 | Novartis Ag | 4-amino-5-phenyl-7-cyclobutyl-pyrrolo (2,3-d) pyrimidine derivatives |
| WO2003024931A1 (en) | 2001-09-14 | 2003-03-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| WO2003024969A1 (en) | 2001-09-14 | 2003-03-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| WO2003035009A2 (en) | 2001-10-26 | 2003-05-01 | Sugen, Inc. | Treatment of acute myeloid leukemia with indolinone compounds |
| WO2003037347A1 (en) | 2001-10-30 | 2003-05-08 | Novartis Ag | Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity |
| WO2003057690A1 (en) | 2001-12-27 | 2003-07-17 | Theravance, Inc. | Indolinone derivatives useful as protein kinase inhibitors |
| WO2003099771A2 (en) | 2002-05-29 | 2003-12-04 | Novartis Ag | Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases |
| WO2004005281A1 (en) | 2002-07-05 | 2004-01-15 | Novartis Ag | Inhibitors of tyrosine kinases |
| WO2004016597A2 (en) | 2002-08-14 | 2004-02-26 | Vertex Pharmaceuticals Incorporated | Protein kinase inhibitors and uses thereof |
| WO2004018419A2 (en) | 2002-08-23 | 2004-03-04 | Chiron Corporation | Benzimidazole quinolinones and uses thereof |
| WO2004039782A1 (ja) | 2002-10-29 | 2004-05-13 | Kirin Beer Kabushiki Kaisha | Flt3自己リン酸化を阻害するキノリン誘導体およびキナゾリン誘導体並びにそれらを含有する医薬組成物 |
| WO2004043389A2 (en) | 2002-11-13 | 2004-05-27 | Chiron Corporation | Methods of treating cancer and related methods |
| WO2004046120A2 (en) | 2002-11-15 | 2004-06-03 | Vertex Pharmaceuticals Incorporated | Diaminotriazoles useful as inhibitors of protein kinases |
| WO2004058749A1 (en) | 2002-12-18 | 2004-07-15 | Vertex Pharmaceuticals Incorporated | Benzisoxazole derivatives useful as inhibitors of protein kinases |
| WO2006138155A1 (en) | 2005-06-10 | 2006-12-28 | Janssen Pharmaceutica N.V. | Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor |
| WO2007048088A2 (en) | 2005-10-18 | 2007-04-26 | Janssen Pharmaceutica N.V. | Method of inhibiting flt3 kinase |
| WO2007109120A2 (en) | 2006-03-17 | 2007-09-27 | Ambit Biosciences Corporation | Imidazolothiazole compounds for the treatment of disease |
| WO2009061446A1 (en) | 2007-11-08 | 2009-05-14 | Ambit Biosciences Corp. | Methods of administering n-(5-tert-butyl-isoxazol-3-yl)-n'-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea to treat proliferative disease |
| WO2009095399A2 (en) | 2008-02-01 | 2009-08-06 | Akinion Pharmaceuticals Ab | Pyrazine derivatives and their use as protein kinase inhbitors |
| WO2011083124A1 (en) | 2010-01-05 | 2011-07-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Flt3 receptor antagonists for the treatment or the prevention of pain disorders |
| WO2016016370A1 (en) * | 2014-07-31 | 2016-02-04 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Flt3 receptor antagonists |
-
2016
- 2016-06-08 EP EP16305669.0A patent/EP3254698A1/en not_active Withdrawn
-
2017
- 2017-06-08 WO PCT/EP2017/063935 patent/WO2017211937A1/en not_active Ceased
- 2017-06-08 HU HUE17727913A patent/HUE062092T2/hu unknown
- 2017-06-08 JP JP2018563716A patent/JP7134097B2/ja active Active
- 2017-06-08 US US16/307,968 patent/US10709687B2/en active Active
- 2017-06-08 EP EP17727913.0A patent/EP3468602B1/en active Active
Patent Citations (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002032861A2 (en) | 2000-10-17 | 2002-04-25 | Merck & Co., Inc. | Orally active salts with tyrosine kinase activity |
| WO2002092599A1 (en) | 2001-05-14 | 2002-11-21 | Novartis Ag | 4-amino-5-phenyl-7-cyclobutyl-pyrrolo (2,3-d) pyrimidine derivatives |
| WO2003024931A1 (en) | 2001-09-14 | 2003-03-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| WO2003024969A1 (en) | 2001-09-14 | 2003-03-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| WO2003035009A2 (en) | 2001-10-26 | 2003-05-01 | Sugen, Inc. | Treatment of acute myeloid leukemia with indolinone compounds |
| WO2003037347A1 (en) | 2001-10-30 | 2003-05-08 | Novartis Ag | Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity |
| WO2003057690A1 (en) | 2001-12-27 | 2003-07-17 | Theravance, Inc. | Indolinone derivatives useful as protein kinase inhibitors |
| WO2003099771A2 (en) | 2002-05-29 | 2003-12-04 | Novartis Ag | Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases |
| WO2004005281A1 (en) | 2002-07-05 | 2004-01-15 | Novartis Ag | Inhibitors of tyrosine kinases |
| WO2004016597A2 (en) | 2002-08-14 | 2004-02-26 | Vertex Pharmaceuticals Incorporated | Protein kinase inhibitors and uses thereof |
| WO2004018419A2 (en) | 2002-08-23 | 2004-03-04 | Chiron Corporation | Benzimidazole quinolinones and uses thereof |
| WO2004039782A1 (ja) | 2002-10-29 | 2004-05-13 | Kirin Beer Kabushiki Kaisha | Flt3自己リン酸化を阻害するキノリン誘導体およびキナゾリン誘導体並びにそれらを含有する医薬組成物 |
| WO2004043389A2 (en) | 2002-11-13 | 2004-05-27 | Chiron Corporation | Methods of treating cancer and related methods |
| WO2004046120A2 (en) | 2002-11-15 | 2004-06-03 | Vertex Pharmaceuticals Incorporated | Diaminotriazoles useful as inhibitors of protein kinases |
| WO2004058749A1 (en) | 2002-12-18 | 2004-07-15 | Vertex Pharmaceuticals Incorporated | Benzisoxazole derivatives useful as inhibitors of protein kinases |
| WO2006138155A1 (en) | 2005-06-10 | 2006-12-28 | Janssen Pharmaceutica N.V. | Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor |
| WO2007048088A2 (en) | 2005-10-18 | 2007-04-26 | Janssen Pharmaceutica N.V. | Method of inhibiting flt3 kinase |
| WO2007109120A2 (en) | 2006-03-17 | 2007-09-27 | Ambit Biosciences Corporation | Imidazolothiazole compounds for the treatment of disease |
| WO2009061446A1 (en) | 2007-11-08 | 2009-05-14 | Ambit Biosciences Corp. | Methods of administering n-(5-tert-butyl-isoxazol-3-yl)-n'-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea to treat proliferative disease |
| WO2009095399A2 (en) | 2008-02-01 | 2009-08-06 | Akinion Pharmaceuticals Ab | Pyrazine derivatives and their use as protein kinase inhbitors |
| WO2011083124A1 (en) | 2010-01-05 | 2011-07-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Flt3 receptor antagonists for the treatment or the prevention of pain disorders |
| WO2016016370A1 (en) * | 2014-07-31 | 2016-02-04 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Flt3 receptor antagonists |
Non-Patent Citations (29)
| Title |
|---|
| "Guidance for Industry - Estimating the Maximum Safe Starting Dose in Initial Clinical Trials for Therapeutics in Adult Healthy Volunteers U.S. Department of Health and Human Services", July 2005, FOOD AND DRUG ADMINISTRATION |
| "Merck Index" |
| BONNINGTON, J. K.; MCNAUGHTON, J. PHYSIOL, vol. 551, pages 433 - 446 |
| BOUDES ET AL., J. NEUROSCI., vol. 29, no. 46, pages 10060 - 10068 |
| BRITISH JOURNAL OF CANCER, vol. 112, 2015, pages 296 - 305 |
| CRITICAL REV IN ONCOL/HEMATOL, vol. 94, 2015, pages 136 - 145 |
| CRITICAL REV IN ONCOL/HEMATOL, vol. 94, 2015, pages 228 - 237 |
| FABIAN ET AL., NAT BIOTECHNOL, vol. 23, 2005, pages 329 - 336 |
| FEHRENBACHER ET AL.: "Curr Protoc Pharmacol.", March 2012 |
| FINNERUP ET AL., LANCET NEUROL., vol. 14, 2015, pages 162 - 173 |
| GATHALIA ET AL., CRITICAL REV IN ONCOL/HEMATOL, vol. 93, 2015, pages 257 - 276 |
| IADAROLA ET AL., PAIN, vol. 35, 1988, pages 313 - 26 |
| KARAMAN ET AL., NAT BIOTECHNOL, vol. 26, 2008, pages 127 - 132 |
| KAYSER ET AL., BRAIN RES, vol. 508, 1990, pages 329 - 332 |
| KIM; CHUNG, PAIN, vol. 50, 1992, pages 355 - 363 |
| LANGE ET AL., BLOOD, vol. 70, 1987, pages 192 - 199 |
| MASSEY ET AL., SUPPORT CARE CANCER, vol. 23, 2015, pages 1827 - 1835 |
| O'FARRELL ET AL., BLOOD, vol. 101, 2003, pages 3597 - 3605 |
| ROSNEY ET AL., ONCOGENE, vol. 6, 1991, pages 1641 - 1650 |
| SANTONI ET AL., INT J CANCER, vol. 135, 2014, pages 763 - 773 |
| STERNBERG ET AL., CURR OPIN HEMATOL, vol. 12, 2005, pages 7 - 13 |
| SWEENEY ET AL: "A phase I study of sunitinib plus capecitabine in pateints with advanced solid tumors", J.CLIN.ONCOL., vol. 28, no. 29, 13 September 2010 (2010-09-13), pages 4513 - 4520, XP002763348, DOI: 10.1200/JCO.2009.26.9696 * |
| TERADA ET AL., PHARMACOLOGY & THERAPEUTICS, vol. 152, 2015, pages 125 - 134 |
| TREEDE ET AL., NEUROLOGY, vol. 70, 2008, pages 1630 - 1635 |
| US FOOD AND DRUG ADMINISTRATION'S GUIDANCE FOR INDUSTRY- ESTIMATING THE MAXIMUM SAFE STARTING DOSE IN INITIAL CLINICAL TRIALS FOR THERAPEUTICS IN ADULT HEALTHY VOLUNTEERS, July 2005 (2005-07-01) |
| US FOOD AND DRUG ADMINISTRATION'S GUIDANCE FOR INDUSTRY- ESTIMATING THE MAXIMUM SAFE STARTING DOSE IN INITIAL CLINICAL TRIALS FOR THERAPEUTICS IN ADULT HEALTHY VOLUNTEERS, July 2005 (2005-07-01), Retrieved from the Internet <URL:http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidan ces/UCM078932.pdf> |
| YOKOTA ET AL., LEUKEMIA, vol. 11, 1997, pages 1605 - 1609 |
| YOUJIN ET AL., LANCET ONCOL, vol. 10, 2009, pages 967 - 74 |
| ZARRINKAR ET AL., BLOOD, vol. 114, 2009, pages 2984 - 2992 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12441707B2 (en) | 2019-12-30 | 2025-10-14 | Tyra Biosciences, Inc. | Indazole compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| US10709687B2 (en) | 2020-07-14 |
| JP2019517536A (ja) | 2019-06-24 |
| EP3468602B1 (en) | 2023-02-22 |
| HUE062092T2 (hu) | 2023-09-28 |
| US20190298691A1 (en) | 2019-10-03 |
| EP3468602A1 (en) | 2019-04-17 |
| JP7134097B2 (ja) | 2022-09-09 |
| EP3254698A1 (en) | 2017-12-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Odaira et al. | Mechanisms underpinning AMP-activated protein kinase-related effects on behavior and hippocampal neurogenesis in an animal model of depression | |
| Bonaventure et al. | Selective blockade of 5-hydroxytryptamine (5-HT) 7 receptors enhances 5-HT transmission, antidepressant-like behavior, and rapid eye movement sleep suppression induced by citalopram in rodents | |
| Shen et al. | Carnosine protects against permanent cerebral ischemia in histidine decarboxylase knockout mice by reducing glutamate excitotoxicity | |
| Nie et al. | Small molecule TrkB agonist deoxygedunin protects nigrostriatal dopaminergic neurons from 6-OHDA and MPTP induced neurotoxicity in rodents | |
| KR20200098536A (ko) | Dux4 발현과 관련된 질병의 치료를 위한 화합물 | |
| US10709687B2 (en) | FLT3 receptor inhibitor at low dosage for the treatment of neuropathic pain | |
| Ding et al. | Involvement of TRPV4-NO-cGMP-PKG pathways in the development of thermal hyperalgesia following chronic compression of the dorsal root ganglion in rats | |
| RS56523B1 (sr) | Tapentadol za sprečavanje i lečenje depresije i anksioznosti | |
| WO2022115798A2 (en) | Compositions and methods for treating migraine | |
| EA030333B1 (ru) | Способ лечения и/или предотвращения расстройств настроения | |
| US20170224716A1 (en) | Methods and Compositions for Treating Pain | |
| JP2017505772A (ja) | spadinのレトロ−インベルソ類似体は増大された抗うつ作用を示す | |
| Sukma et al. | CNS inhibitory effects of barakol, a constituent of Cassia siamia Lamk | |
| JP6959371B2 (ja) | 純粋な5−ht6受容体アンタゴニストの新たな使用 | |
| KR102712565B1 (ko) | Gabaa 수용체 리간드 | |
| JP2014141502A (ja) | センタキンを用いた新規の治療方法 | |
| Gogos et al. | Role of serotonin-1A receptors in the action of antipsychotic drugs: comparison of prepulse inhibition studies in mice and rats and relevance for human pharmacology | |
| Warner et al. | California dreamin''bout endothelin: emerging new therapeutics | |
| Pan et al. | Salidroside ameliorates orthopedic surgery-induced cognitive dysfunction by activating adenosine 5′-monophosphate-activated protein kinase signaling in mice | |
| Uzbay et al. | Acute and chronic tianeptine treatments attenuate ethanol withdrawal syndrome in rats | |
| Tian et al. | Preclinical pharmacology of TP1, a novel potent triple reuptake inhibitor with antidepressant properties | |
| Okuda et al. | Trazodone hydrochloride attenuates thermal hyperalgesia in a chronic constriction injury rat model | |
| CN101879151A (zh) | 大黄素在制备p2x3介导神经病理痛/神经系统疾病药物中的应用 | |
| Mashayekhpour et al. | Neuroprotective effects of nanophytosome-encapsulated citral in a mouse model of chronic unpredictable mild stress through the suppression of oxidative stress and inflammation | |
| Zhu et al. | Non-adrenergic exploratory behavior induced by moxonidine at mildly hypotensive doses |
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: 17727913 Country of ref document: EP Kind code of ref document: A1 |
|
| ENP | Entry into the national phase |
Ref document number: 2018563716 Country of ref document: JP Kind code of ref document: A |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| ENP | Entry into the national phase |
Ref document number: 2017727913 Country of ref document: EP Effective date: 20190108 |