MedPath

Vilazodone

Generic Name
Vilazodone
Brand Names
Viibryd
Drug Type
Small Molecule
Chemical Formula
C26H27N5O2
CAS Number
163521-12-8
Unique Ingredient Identifier
S239O2OOV3

Overview

Vilazodone is a novel compound with combined high affinity and selectivity for the 5-hydroxytryptamine (5-HT) transporter and 5-HT(1A) receptors. Vilazodone may also be associated with less sexual dysfunction and weight gain. Vilazodone was given FDA approval on January 21, 2011.

Indication

用于治疗成人重度抑郁症(MDD)。

Associated Conditions

  • Major Depressive Disorder (MDD)

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/10/16
Phase 4
Not yet recruiting
2023/07/19
N/A
Completed
Mental Health Services in the Capital Region, Denmark
2023/07/17
Phase 2
Not yet recruiting
Global Coalition for Adaptive Research
2023/07/03
Not Applicable
Recruiting
First Affiliated Hospital of Zhejiang University
2022/09/13
N/A
Recruiting
University Hospital Muenster
2022/06/16
Phase 2
Recruiting
Global Coalition for Adaptive Research
2022/05/02
N/A
UNKNOWN
2022/03/07
Phase 1
Withdrawn
2021/04/05
N/A
UNKNOWN
2021/02/10
Phase 2
Active, not recruiting
Ajay Wasan, MD, Msc

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Allergan, Inc.
0456-1110
ORAL
10 mg in 1 1
4/1/2024
Apotex Corp
60505-4774
ORAL
40 mg in 1 1
7/28/2023
NorthStar RxLLC
72603-127
ORAL
40 mg in 1 1
12/2/2022
Accord Healthcare Inc.
16729-352
ORAL
10 mg in 1 1
12/13/2023
NorthStar RxLLC
72603-126
ORAL
20 mg in 1 1
12/2/2022
Exelan Pharmaceuticals Inc.
76282-546
ORAL
40 mg in 1 1
3/27/2023
Novadoz Pharmaceuticals LLC
72205-261
ORAL
20 mg in 1 1
6/30/2023
Cipla USA Inc.
69097-981
ORAL
20 mg in 1 1
1/9/2023
Teva Pharmaceuticals, Inc.
0480-2043
ORAL
40 mg in 1 1
1/31/2022
NorthStar RxLLC
72603-125
ORAL
10 mg in 1 1
12/2/2022

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

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