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Evenamide

From Wikipedia, the free encyclopedia
Investigational antipsychotic drug

This article needs to beupdated. Please help update this article to reflect recent events or newly available information.(August 2025)
Pharmaceutical compound
Evenamide
Clinical data
Other namesNW-3509; NW-3509A
Routes of
administration
oral
ATC code
  • None
Identifiers
  • 2-[2-(3-butoxyphenyl)ethylamino]-N,N-dimethylacetamide
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H26N2O2
Molar mass278.396 g·mol−1
3D model (JSmol)
  • CCCCOc1cccc(CCNCC(=O)N(C)C)c1
  • InChI=1S/C16H26N2O2/c1-4-5-11-20-15-8-6-7-14(12-15)9-10-17-13-16(19)18(2)3/h6-8,12,17H,4-5,9-11,13H2,1-3H3
  • Key:GRHBODILPPXVKN-UHFFFAOYSA-N

Evenamide (INNTooltip International Nonproprietary Name) (developmental code namesNW-3509,NW-3509A)[1] is aselectivevoltage-gated sodium channelblocker, including (and not limited to) subtypesNav1.3,Nav1.7, andNav1.8, which is described as anantipsychotic and is under development by Newron Pharmaceuticals as anadd-on therapy for the treatment ofschizophrenia.[2][3][4][5] The drug has shown efficacy inanimal models ofpsychosis,mania,depression, andaggression.[4] It has completedphase Iclinical trials, andphase II clinical trials will be commenced in the third quarter of 2015.[6]

The drug was discovered by Newron Pharmaceuticals SpA, a pharmaceutical company located in Italy[7]

Clinical studies

[edit]

In a randomized study with treatment-resistant schizophrenia patients, evenamide was added to the treatment regimen, with the psychological assessors beingblinded to whether evenamide was taken. 70% of the participants reported a significant lowering of their impairments; and in 25%, schizophrenia went in full remission. A full double-blind phase III study with treatment-resistant schizophrenia patients is in preparation as of January 2023.[8]

The 4 week placebo trial of 2021 to evaluate the safety, tolerability and preliminary evidence of efficacy of evenamide for people with chronic schizophrenia was selected to address patients who are receiving treatment at constant doses of one of the following atypical antipsychotics: aripiprazole, clozapine, quetiapine, olanzapine, paliperidone or risperidone.[9][10]

See also

[edit]

References

[edit]
  1. ^Singh R, Hahn MK, Bansal Y, Agarwal SM, Remington G (February 2024)."Evenamide: A Potential Pharmacotherapeutic Alternative for Treatment-Resistant Schizophrenia".The International Journal of Neuropsychopharmacology.27 (2) pyae005.doi:10.1093/ijnp/pyae005.PMC 10858345.PMID 38195245.
  2. ^"Drug Development in Schizophrenia: Summary and Table".Pharmaceutical Medicine.28 (5):265–271. 2014.doi:10.1007/s40290-014-0070-6.ISSN 1178-2595.S2CID 8513976.
  3. ^Kemp MI (2010). "Structural trends among second-generation voltage-gated sodium channel blockers".Progress in Medicinal Chemistry.49:81–111.doi:10.1016/S0079-6468(10)49003-7.ISBN 978-0-12-381292-6.PMID 20855039.
  4. ^abZuliani V, Amori L, Rivara M (21 June 2011)."Advances in Design of Development of Sodium Channel Blockers". In Gupta SP (ed.).Ion Channels and Their Inhibitors. Springer Science & Business Media. pp. 102–.ISBN 978-3-642-19922-6.
  5. ^Zuliani V, Amori L, Rivara M (2011). "Advances in Design and Development of Sodium Channel Blockers".Ion Channels and Their Inhibitors. pp. 79–115.doi:10.1007/978-3-642-19922-6_4.ISBN 978-3-642-19921-9.
  6. ^"Newron raised new funds to continue the development of Neurological therapies".Labiotech. 5 February 2015. Archived fromthe original on 4 March 2016.
  7. ^"Newron announces positive top-line results from potentially pivotal Phase II/III study 008A with evenamide in schizophrenia patients".Newron Pharmaceuticals. Retrieved2024-06-28.
  8. ^"Newron reports exceptional one-year results of study 014/15 with evenamide in treatment-resistant schizophrenia (TRS)". Newron Pharmaceuticals. 2024-01-04. Retrieved2024-01-04.
  9. ^"ClinicalTrials.gov".clinicaltrials.gov. 17 May 2021. Retrieved2024-06-28.
  10. ^"Evenamide: New Positive Results From Study 008A".Psychiatric Times. 2024-04-30. Retrieved2024-06-28.

External links

[edit]
Typical
Disputed
Atypical
Others
Calcium
VDCCsTooltip Voltage-dependent calcium channels
Blockers
Activators
Potassium
VGKCsTooltip Voltage-gated potassium channels
Blockers
Activators
IRKsTooltip Inwardly rectifying potassium channel
Blockers
Activators
KCaTooltip Calcium-activated potassium channel
Blockers
Activators
K2PsTooltip Tandem pore domain potassium channel
Blockers
Activators
Sodium
VGSCsTooltip Voltage-gated sodium channels
Blockers
Activators
ENaCTooltip Epithelial sodium channel
Blockers
Activators
ASICsTooltip Acid-sensing ion channel
Blockers
Chloride
CaCCsTooltip Calcium-activated chloride channel
Blockers
Activators
CFTRTooltip Cystic fibrosis transmembrane conductance regulator
Blockers
Activators
Unsorted
Blockers
Others
TRPsTooltip Transient receptor potential channels
LGICsTooltip Ligand gated ion channels
Phenethylamines
Amphetamines
Phentermines
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Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
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