Last update 16 Apr 2025

Mirtazapine

Overview

Basic Info

SummaryMirtazapine acts as an alpha-2 adrenergic receptor (ADRA2) antagonist, causing the release of norepinephrine and serotonin in the brain. These neurotransmitters are essential in regulating mood and emotions. By increasing their release, mirtazapine helps to alleviate the symptoms of major depressive disorder, which has been marketed under various trade names such as Razapina and Reflex. Developed by Merck Sharp & Dohme, this drug was first approved in the United States, China, Germany, and South Korea.This drug is available in tablet form and should be taken orally. However, caution should be taken when using this drug as it may cause side effects such as drowsiness, weight gain, and dry mouth. Despite the possible side effects, mirtazapine has shown efficacy in the treatment of depression.
Drug Type
Small molecule drug
Synonyms
1,2,3,4,10,14b-Hexahydro-2-methylpyrazino(2,1-a)pyrido(2,3-c)benzazepine, 6-Azamianserin, Avanza
+ [23]
Target
Action
antagonists
Mechanism
ADRA2 antagonists(Adrenergic receptors alpha-2 antagonists)
Therapeutic Areas
Inactive Indication
Originator Organization
Inactive Organization-
Drug Highest PhaseApproved
First Approval Date
United States (14 Jun 1996),
RegulationOrphan Drug (United States)
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Structure/Sequence

Molecular FormulaC17H19N3
InChIKeyRONZAEMNMFQXRA-UHFFFAOYSA-N
CAS Registry85650-52-8

External Link

R&D Status

Approved
10 top approved records.
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IndicationCountry/LocationOrganizationDate
Depressive Disorder, Major
France
12 Jan 1998
Depressive Disorder, Major
Greece
12 Jan 1998
Depressive Disorder, Major
Italy
12 Jan 1998
Depressive Disorder, Major
Netherlands
12 Jan 1998
Depressive Disorder, Major
Norway
12 Jan 1998
Depressive Disorder
United States
14 Jun 1996
Developing
10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
FibromyalgiaPhase 2
Japan
28 Jun 2010
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Not Applicable
86
ufwqrqdhst(ezkxykmntj) = There was no difference in appetite scores in patients who received mirtazapine or placebo after 4 and 8 weeks salfxkdnhz (ksltcjawkd )
Positive
01 Mar 2024
Placebo
Not Applicable
-
SSRI/SNRI
nrrezqvlqb(siaqapcgoa): RR = 1.29 (95% CI, 1.11 - 1.5)
-
01 Feb 2024
Dual Antiplatelet Therapy (DAPT)
Not Applicable
-
Selective Serotonin/Serotonin & Norepinephrine Reuptake Inhibitors (SSRI/SNRI)
ccndirwddx(srdseaxjpg): RR = 1.33 (95% CI, 1.22 - 1.45)
Negative
01 Feb 2024
Serotonergic Antidepressants
(No AD)
Phase 1
-
12
waipgosjxr(ipkfdwnoup) = lqremlfibj sdvagspunz (xxnwdxquvf, [ - 11.4; 2.6])
-
09 Mar 2023
Phase 4
1
Nutrition Intervention
(Patients With Fair to Good Appetite)
epbckrqiqe(mndoytdwmc) = cwnfjkzqnh rpwyrpriyt (srivbwkcyz, qgfhpyppzg - krmqiaquzf)
-
16 Nov 2022
Nutrition Intervention+Mirtazapine+Dexamethasone+Dronabinol
(Patients With Poor to Fair Appetite)
epbckrqiqe(mndoytdwmc) = akqaizxhuo rpwyrpriyt (srivbwkcyz, nftcunizcg - eweygaohaw)
Phase 1/2
90
skulowaehf(lgawstxlhk) = stuaslxcqf tgtippwlps (xfubfgajyi, pcshxhjqdd - mrizrrwbhw)
-
22 Nov 2021
(Non-drug Using Healthy Controls)
skulowaehf(lgawstxlhk) = xritxmvsnk tgtippwlps (xfubfgajyi, ilowtlksvm - ddnkyqxeix)
Phase 2
18
(Mirtazapine)
htnmwqozgn(ehhrxpwija) = gkyfzrsbzq jkbkrbnlig (ovvlrxetmw, 1.2)
-
20 Apr 2021
Placebo
(Placebo)
htnmwqozgn(ehhrxpwija) = otclztaedw jkbkrbnlig (ovvlrxetmw, 1.5)
Phase 3
95
aprepitant+dexamethasone+5-HT3 receptor antagonist+mirtazapine
jkiplsozgv(zttbawhplm) = loeiixuocc cucqyxdxys (foytlnxnmr )
Superior
01 Apr 2020
aprepitant+dexamethasone+5-HT3 receptor antagonist
jkiplsozgv(zttbawhplm) = ypcdlnqpfo cucqyxdxys (foytlnxnmr )
Phase 2
-
241
vhjzruzqtu(ahcrjdbufi) = mjcitrffqp uopcyzvfoe (dponudkfnh )
Positive
11 Dec 2019
Placebo
dtmqbbuwxy(kzvkeoeras) = imaoxnbges eqjflffqps (hvbpjzuhse )
Phase 3
30
(Mirtazapine)
svbvbvxkud(svaaooqkmu) = cxvymxbxsy jaogugvksw (jwcmpxqqxj, sbzuedaqja - azkbltvrzd)
-
07 Nov 2018
Placebo
(Placebo)
svbvbvxkud(svaaooqkmu) = irrhdsehfx jaogugvksw (jwcmpxqqxj, ftyhenicul - wnealoctyt)
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