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 PDF

Info

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
Application number
PCT/EP2017/063935
Other languages
English (en)
French (fr)
Inventor
Jean Valmier
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Biodol Therapeutics
Institut National de la Sante et de la Recherche Medicale INSERM
Universite de Montpellier
AxLR SATT du Languedoc Roussillon SAS
Original Assignee
Biodol Therapeutics
Institut National de la Sante et de la Recherche Medicale INSERM
Universite de Montpellier
AxLR SATT du Languedoc Roussillon SAS
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
Application filed by Biodol Therapeutics, Institut National de la Sante et de la Recherche Medicale INSERM, Universite de Montpellier, AxLR SATT du Languedoc Roussillon SAS filed Critical Biodol Therapeutics
Priority to JP2018563716A priority Critical patent/JP7134097B2/ja
Priority to US16/307,968 priority patent/US10709687B2/en
Priority to EP17727913.0A priority patent/EP3468602B1/en
Publication of WO2017211937A1 publication Critical patent/WO2017211937A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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
    • A61K31/40Heterocyclic 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
    • A61K31/403Heterocyclic 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
    • A61K31/404Indoles, e.g. pindolol
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further 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
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0053Mouth and digestive tract, i.e. intraoral and peroral administration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/70Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
    • A61K9/7023Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P23/00Anaesthetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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

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)
PCT/EP2017/063935 2016-06-08 2017-06-08 Flt3 receptor inhibitor at low dosage for the treatment of neuropathic pain Ceased WO2017211937A1 (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (22)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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