Vanda Pharmaceuticals

Vanda Pharmaceuticals

VNDAApproved
Washington DC, United StatesFounded 2003vandapharma.com

Founded in 2003 and publicly traded on NASDAQ (VNDA), Vanda Pharmaceuticals leverages genetics and genomics to inform drug discovery and development. The company has achieved significant milestones with FDA approvals for Fanapt® (2009) and HETLIOZ® (2014), and continues to expand its pipeline with late-stage candidates like tradipitant and imsidolimab. Vanda's strategic focus combines commercial execution with a science-driven approach to address complex disorders in circadian rhythms, psychiatry, and inflammation.

Market Cap
$417.9M
Founded
2003
Focus
Small Molecules

VNDA · Stock Price

USD 7.074.39 (-38.31%)

Historical price data

AI Company Overview

Founded in 2003 and publicly traded on NASDAQ (VNDA), Vanda Pharmaceuticals leverages genetics and genomics to inform drug discovery and development. The company has achieved significant milestones with FDA approvals for Fanapt® (2009) and HETLIOZ® (2014), and continues to expand its pipeline with late-stage candidates like tradipitant and imsidolimab. Vanda's strategic focus combines commercial execution with a science-driven approach to address complex disorders in circadian rhythms, psychiatry, and inflammation.

Technology Platform

Utilizes genetics, genomics, and pharmacogenetics to inform drug discovery, clinical trial design, and commercial positioning, aiming to identify genetic factors that enhance therapeutic efficacy and safety.

Pipeline Snapshot

77

77 drugs in pipeline, 31 in Phase 3

DrugIndicationStage
IloperidoneSchizophreniaApproved
tasimelteon 20 mg capsule + tasimelteon 2 mg I.V.Non-24-Hour-Sleep-Wake DisorderApproved
Tradipitant + Placebo + Open Label TradipitantIdiopathic GastroparesisPhase 3
ImsidolimabGeneralized Pustular PsoriasisPhase 3
Iloperidone + PlaceboSchizophreniaPhase 3

Funding History

3

Total raised: $80M

IPO$50MUndisclosedApr 27, 2006
Series B$20MUndisclosedJun 15, 2004
Series A$10MUndisclosedJan 15, 2003

FDA Approved Drugs

4
PONVORYNDAMar 18, 2021
HETLIOZ LQNDADec 1, 2020
HETLIOZNDAJan 31, 2014

Opportunities

Significant near-term opportunities include the commercial launch of newly approved BYSANTI™, potential FDA approval and market expansion for HETLIOZ® into the large Jet Lag Disorder market, and the approval of imsidolimab for generalized pustular psoriasis.
Lifecycle management of existing products through new formulations and indications provides additional growth avenues.

Risk Factors

Key risks include regulatory setbacks for late-stage pipeline candidates, challenging commercialization against larger competitors, potential generic competition for core products, and the inherent uncertainty of clinical trial outcomes.
The company's concentrated pipeline and reliance on a few key assets also present financial and operational risks.

Competitive Landscape

Vanda competes with large pharmaceutical companies in psychiatry (e.g., Johnson & Johnson, Otsuka) and immunology, and faces potential competition in circadian disorders. Its differentiation is based on a targeted, genetics-informed development strategy and first-in-class/movel mechanism assets like HETLIOZ® and BYSANTI™, but it must navigate markets dominated by players with greater commercial scale.

Publications
20
Patents
20
Pipeline
77
FDA Approvals
4

Company Info

TypeTherapeutics
Founded2003
LocationWashington DC, United States
StageApproved
RevenueRevenue Generating

Trading

TickerVNDA
ExchangeNASDAQ

Therapeutic Areas

PsychiatrySleep DisordersCircadian Rhythm DisordersDermatologyGastroenterologyOncologyImmunology
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