NEWER DRUGS
TREATMENTS FOR DEPRESSION AND ANXIETY
Drug Name
|
Pharmacologic Action
|
Company
|
Indication
|
Developmental Phase
|
Vilazodone
|
5-HT1A
partial agonist, serotonin reuptake inhibitor
|
Clinical
Data Online, Inc.
|
Depression
|
NDA anticipated in late 2009
|
Valdoxan (agomelatine,
AGO 178)
|
5-HT2C
antagonist, 5-HT2B antagonist, melatonin M1/M2 receptor agonist
|
Servier, Novartis
|
Depression,
anxiety
|
US: Phase III; EU: available as of mid-2009
|
Lu AA21004
|
5-HT3
antagonist, 5-HT1A partial agonist
|
Lundbeck
|
Depression,
anxiety
|
Phase III (results not expected until 2011)
|
LY2216684
|
Norepinephrine
reuptake inhibitor
|
Eli
Lilly
|
Depression,
ADHD
|
Phase III
|
SEP-227162
|
DA/NE/5-HT
reuptake inhibitor
|
Sepracor
|
Depression,
anxiety
|
Phase III
|
F2695, levomilnacipran
|
enantiomer
of milnacipran
|
Forest
Labs, Pierre Fabre
|
Depression
|
Phase II
|
Lu AA24530
|
5-HT3
and 5-HT2C antagonist, serotonin reuptake inhibitor
|
Lundbeck
|
Depression,
anxiety
|
Phase II
|
SEP-225289
|
DA/NE/5-HT
reuptake inhibitor
|
Sepracor
|
Depression,
anxiety
|
Phase II
|
Losmapimod, GSK 856553
|
P38
kinase inhibitor
|
GSK
|
Depression
|
Phase II
|
GW823296 (orvepitant)
|
NK1
antagonist
|
GSK
|
Depression,
anxiety
|
Phase II
|
AZD6765
|
NMDA
antagonist
|
AstraZeneca
|
Depression,
anxiety
|
Phase II
|
TC-5214
|
Nonselective
Nicotinic acetylcholine receptor antagonist
|
Targacept
|
Depression
|
Phase II
|
ONO-2333Ms
|
CRF1
antagonist
|
Ono
Pharmaceuticals
|
Depression,
anxiety
|
Phase II
|
Nemifitide
(INN 00835) |
Pentapeptide
analog of melanocyte-inhibiting factor (MIF-1) administered intravenously
(mechanism unknown)
|
Tetragenex
|
Depression
|
Phase II
|
SSR 411298
|
FAAH
(fatty acid amide hydrolase) inhibitor
|
Sanofi-Aventis
|
Depression
(in the elderly)
|
Phase II
|
ORG 26576
|
AMPA
receptor modulator
|
Schering-Plough
|
Depression
|
Phase II
|
TIK-101/d-cycloserine
|
NMDA
anatagonist
|
Tikvah
Pharmaceuticals
|
Anxiety,
OCD
|
Phase II
|
ORG 34517/34850
|
Glucocorticoid
receptor type II (GRII) antagonist
|
Schering-Plough
|
Depression,
psychosis
|
Phase II
|
GSK561679
|
CRF1
antagonist
|
GSK
|
Depression
(in wom
|
Phase II
|
Tyrima™, CX157
|
Reversible
monoamine oxidase A (MAO-A) inhibitor
|
CeNeRx
|
Depression,
anxiety
|
Phase II
|
RO4917523, EVT101
|
NMDA
antagonist
|
Evotec, Roche
|
Depression
|
Phase II
|
GSK 588045
|
5-HT1
antagonist
|
GSK
|
Depression,
anxiety
|
Phase II
|
RX-10100
|
Unknown
serotonin and dopamine modulator
|
Rexahn
|
Depression
|
Phase II
|
AZD7325
|
GABA
receptor partial agonist
|
AstraZeneca
|
Anxiety
|
Phase II
|
AZD2327
|
Enkephalinergic
modulator
|
AstraZeneca
|
Anxiety
|
Phase II
|
SA4503
|
Sigma
receptor agonist
|
Eisai, M's Science
|
Depression,
post-stroke recovery
|
Phase II (Europe)
|
PRE703
|
MgluR
agonist
|
Prescient
|
Anxiety
|
Phase I
|
JNJ-19567470, TS-041
|
CRF1
antagonist
|
Janssen (Johnson &
Johnson), Taisho
|
Depression,
anxiety
|
Phase I
|
SSR 125543
|
CRF1
antagonist
|
Sanofi-Aventis
|
Depression,
anxiety, hyperphagia
|
Phase I
|
GSK 163090
|
5-HT1
antagonist
|
GSK
|
Depression,
anxiety
|
Phase I
|
TC-2216
|
Nicotinic
acetylcholine receptor (alpha4beta2) antagonist
|
Targacept
|
Depression
|
Phase I
|
URB597
|
FAAH
(fatty acid amide hydrolase) inhibitor
|
Schering-Plough
|
Depression
|
Phase I
|
AZD6280
|
GABA
receptor partial agonist
|
AstraZeneca
|
Anxiety
|
Phase I
|
TREATMENTS FOR SLEEP DISORDERS
Drug Name
|
Pharmacologic Action
|
Company
|
Indication
|
Developmental Phase
|
Ciltyri®, Eplivanserin, SR 46349
|
5-HT2A
receptor antagonist
|
Sanofi-Aventis
|
Sleep
disorders
|
US/EU decisions expected in 4th quarter 2009
|
ORG 50081 (esmirtazapine)
|
5-HT2
antagonist, H1 antagonist, alpha-2-adrenoceptor antagonist
|
Schering-Plough
|
Sleep
disorders, hot flashes
|
Phase III
|
Tasimelte, VEC-162
|
Melatonin
receptor agonist
|
Vanda Pharmaceuticals
|
Sleep
disorders, depression
|
Phase III
|
Almorexant, ACT-078573
|
Orexen
OX1 and OX2 receptor antagonist
|
Actelion
|
Sleep
disorders
|
Phase III
|
PD-6735
|
Melatonin
receptor agonist
|
Phase
2 Discovery
|
Sleep
Disorders
|
Phase II
|
Pimavanserin, ACP-103
|
Serotonin
5-HT2A receptor inverse agonist, dopamine D2/D3 receptor partial agonist, acetylcholine
M1 receptor agonist
|
Acadia
|
Sleep
disorders, Parkinson's disease psychosis, schizophrenia co-therapy
|
Phase II
|
PD-200,390
|
Voltage-gated
calcium channel alpha(2)delta subunit modulator
|
Pfizer
|
Sleep
disorders
|
Phase II
|
EVT 201
|
GABA-A
partial agonist
|
Evotec
|
Sleep
disorders
|
Phase II
|
LY2624803, HY10275
|
5-HT2A
and histamine H1 receptor antagonist
|
Eli
Lilly, Hypnion
|
Depression,
ADHD
|
Phase II
|
TIK-301, LY156735
|
Melatonin
agonist, 5-HT2B/5-HT2C antagonist
|
Tikvah
Pharmaceuticals
|
Sleep
disorders
|
Phase II
|
TREATMENTS FOR PSYCHOSIS/BIPOLAR DISORDER
Drug Name
|
Pharmacologic Action
|
Company
|
Indication
|
Developmental Phase
|
Fanapt ® (iloperidone)
|
5-HT2A
antagonist, D2/D3 antagonist, alpha-1-adrenoceptor antagonist
|
Vanda
Pharmaceuticals
|
Psychosis
|
Approved 5/6/09
|
Saphris™ (asenapine, ORG 5222)
|
5-HT2
antagonist, D2 partial agonist
|
Schering-Plough
|
Psychosis
|
NDA Submitted, approval expected by mid-2009
|
Serdolect®, sertindole
|
5-H2
antagonist, 5-HT6 antagonist, D2 antagonist, afects alpha-1-adrenoceptor
|
Lundbeck
|
Psychosis
|
NDA Submitted (approved in EU)
|
Bifeprunox (DU-127090)
|
Partial
agonist at dopamine D2 and serotonin 5-HT1A receptors
|
Solvay, Wyeth
|
Psychosis
|
Phase III (resubmission planned for 2009)
|
Corlux ® (AKA
mifepristone or RU-486)
|
Glucocorticoid
receptor type II (GRII) antagonist, progesterone receptor antagonist
|
Corcept
|
Psychosis,
depression
|
Phase III
|
Pardoprunox, SLV 308
|
D2
partial agonist, 5-HT1A agonist
|
Solvay
|
Psychosis,
Parkinson's disease
|
Phase III
|
LIC477D (licarbazepine)
|
Voltage-gated
sodium channel inhibitor
|
Novartis
|
Psychosis
|
Phase III
|
Pimavanserin, ACP-103
|
Serotonin
5-HT2A receptor inverse agonist, dopamine D2/D3 receptor partial agonist,
acetylcholine M1 receptor agonist
|
Acadia
|
Antipsychotic-induced
side effects, Parkinson's disease psychosis
|
Phase III
|
ORG 34517/34850
|
Glucocorticoid
receptor type II (GRII) antagonist
|
Schering-Plough
|
Depression,
psychosis
|
Phase II
|
ORG 24448
|
AMPA
modulator
|
Schering-Plough/Cortex
|
Psychosis
|
Phase II
|
Lurasidone (SM 13496)
|
D2,
5-HT2A antagonist
|
Merck, Dainippon
Sumitomo
|
Psychosis
|
Phase II
|
RG2417 (triacetyluridine)
|
Prodrug
of uridine
|
Repligen
|
Bipolar
disorder
|
Phase II
|
Lonasen (blonanserin)
|
D2,
5-HT2A antagonist
|
Dainippon
Sumitomo
|
Psychosis
|
Phase II
|
R1678
|
mGluR
modulator
|
Roche
|
Psychosis
|
Phase II
|
LY2140023
|
Prodrug
for an mGluR2/3 agonist
|
Eli
Lilly
|
Psychosis
|
Phase II
|
Mirapex ® (pramipexole)
|
Dopamine
D2, D3 receptor agonist
|
Boehringer-Ingelheim
|
Bipolar
Disorder
|
Phase II
|
Lu-31-130
|
D1
antagonist, D2 antagonist, 5-HT2A antagonist
|
Lundbeck
|
Psychosis
|
Phase II
|
Caripazine, RGH-188
|
D2,
D3 antagonist
|
Forest
Labs
|
Psychosis
|
Phase II
|
Talnetant (SB-223412)
|
NK-3
antagonist
|
GSK
|
Psychosis,
IBS, overactive bladder
|
Phase II
|
AVE1625
|
CB1
antagonist
|
Sanofi-Aventis
|
Psychosis
|
Phase II
|
GW742457
|
5-HT6
antagonist
|
GSK
|
Psychosis,
Alzheimer's
|
Phase II
|
vabicaserin (SCA-136)
|
5-HT2C
agonist
|
Wyeth
|
Schizophrenia
|
Phase II
|
P-101
|
Alpha-2-adrenoceptor
antagonist
|
Potomac
Pharma
|
Schizophrenia
|
Phase II
|
ORG 25935
|
GLYT1
(glycine transporter) inhibitor
|
Schering-Plough
|
Psychosis
|
Phase II
|
RG1068, secretin
|
Endogenous
pancreatic hormone
|
Repligen
|
Psychosis,
autism, anxiety
|
Phase II
|
ADX63365
|
MGluR
agonist
|
Merck
|
Psychosis
|
Phase II
|
BL-1020
|
GABA-A
agonist
|
BioLineRx
|
Psychosis
|
Phase II
|
TS-032
|
5-HT2A
antagonist
|
Pfizer
|
Psychosis
|
Phase II
|
PF-217830
|
D3
antagonist
|
Pfizer
|
Psychosis
|
Phase II
|
PF-2545920
|
D3
antagonist
|
Pfizer
|
Psychosis
|
Phase II
|
SLV 313
|
5-HT2A
antagonist
|
Solvay
|
Psychosis
|
Phase II
|
ABT-089
|
Nicotinic
acetylcholine receptor agonist
|
Abbott
Laboratories
|
Psychosis,
ADHD
|
Phase I
|
GW773812
|
D2,
5-HT antagonist
|
GSK
|
Psychosis
|
Phase I
|
SSR 103800
|
GLYT1
(Type 1 glycine transporter) inhibitor
|
Sanofi-Aventis
|
Psychosis
|
Phase I
|
TC-1827
|
Selective
alpha4beta2 nicotinic acetylcholine receptor agonist
|
Targacept
|
Cognitive
impairment associated with schizophrenia
|
Phase I
|
JNJ-17305600
|
GLYT1
inhibitor
|
Johnson
& Johnson
|
Psychosis
|
Phase I
|
XY 2401
|
Glycine
site specific NMDA modulator
|
Xytis
|
Psychosis
|
Phase I
|
PNU 170413
|
D3
antagonist
|
Pfizer
|
Psychosis
|
Phase I
|
RGH-188
|
D2,
D3 antagonist
|
Forrest
|
Psychosis
|
Phase I
|
Read more about Depression and Anxiety Click here
REFERENCES:
1.
YK Wing, Recent advances in the
management of depression and Psychopharmacology , HKMJ 2000;6:85-92
2. Sanjay J Mathew, Husseini K Manji and Dennis S Charney ,Novel Drugs and Therapeutic Targets for Severe Mood Disorders; Neuropsychopharmacology (2008), 1–13.
3. JOHANNE ROSE L.AC. A; Natural Approach to Depression ,
CLINICAL NUTRITION INSIGHTS Vol.6,
No. 4
4. Joseph A. Lieberman III,
History of the Use of Antidepressants in Primary Care Companion, J Clin Psychiatry 2003;5[suppl 7]:6–10
5. Madhukar H Trivedi, MD and Ella J Daly, MB, MRC ; Psych Treatment Strategies and Tactics for Treatment-resistant
Depression, ©
T O U C H B R I E F I N G S 2 0 0 7.
6. A report byThe British Psychological
Society ;Division of Clinical psychology recent advances in understanding mentalillness and
psychotic experiences
By: Krishna kumar gokavarapu
BITS Pilani (M.Pharm)
Tags:
Pharmacology
Almorexant(ACT078573) is a potent and competitive dual orexin 1 receptor (OX1)/orexin 2 receptor (OX2) antagonist with Ki values of 1.3 and 0.17 nM for OX1 and OX2, respectively. Almorexant
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