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VNDA

Vanda Pharmaceuticals Inc.

$4.75
0.24
 (5.32%)
Exchange:   NASDAQ
Market Cap:   280.673M
Shares Outstanding:   469.97M
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About The Company

Sector:  Healthcare
Industry:  Biotechnology
   
CEO:  Mihael H. Polymeropoulos
Full Time Employees:  368
Address: 
2200 Pennsylvania Avenue NW
Washington
DC
20037
US
Website:  https://www.vandapharma.com
Vanda Pharmaceuticals Inc., a biopharmaceutical company, focuses on the development and commercialization of therapies to address high unmet medical needs. The company’s marketed products include HETLIOZ for the treatment of non-24-hour sleep-wake disorders; and Fanapt oral tablets for the treatment of schizophrenia. Its products under development include HETLIOZ (tasimelteon) for the treatment of jet lag disorder, smith-magenis syndrome, pediatric Non-24, autism spectrum, and delayed sleep phase disorder; Fanapt (iloperidone) for the treatment of bipolar disorder and a long acting injectable formulation program for the treatment of schizophrenia; and Tradipitant (VLY-686), a small molecule neurokinin-1 receptor (NK-1R) antagonist, for the treatment of atopic dermatitis, gastroparesis, and motion sickness. The company’s products under development also comprise VTR-297, a small molecule histone deacetylase inhibitor for the treatment of hematologic malignancies and with potential use as a treatment for various oncology indications; VQW-765, a small molecule nicotinic acetylcholine receptor partial agonist for the treatment of psychiatric disorders; a portfolio of cystic fibrosis transmembrane conductance regulator activators and inhibitors for the treatment of dry eye and ocular inflammation, as well as BPO-27 for the treatment of secretory diarrhea disorders, including cholera; and VHX-896, the active metabolite of iloperidone. It markets its products in the United States, Europe, and Israel. Vanda Pharmaceuticals Inc. was incorporated in 2002 and is headquartered in Washington, the District of Columbia.

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Relevant news

21-08-2025 16:40
Vanda Seeks FDA Commissioner Review of Outgoing CDER Director’s Decision to Uphold Approval of Two Generic Versions of Hetliozยฎ