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VNDA Overview

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$
0.000
0.000(0.000%)
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0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

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High
9.940
Open
8.950
VWAP
9.47
Vol
3.81M
Mkt Cap
565.07M
Low
8.910
Amount
36.09M
EV/EBITDA(TTM)
--
Total Shares
59.11M
EV
256.69M
EV/OCF(TTM)
--
P/S(TTM)
2.37
Vanda Pharmaceuticals Inc. is a global biopharmaceutical company focused on the development and commercialization of therapies to address unmet medical needs and improve the lives of patients. The Company’s commercial portfolio consist of three products: Fanapt for the acute treatment of manic or mixed episodes associated with bipolar I disorder and the treatment of schizophrenia, HETLIOZ for the treatment of Non-24-Hour Sleep-Wake Disorder (Non-24) and for the treatment of nighttime sleep disturbances in Smith-Magenis syndrome (SMS) and PONVORY for the treatment of relapsing forms of multiple sclerosis (RMS), including clinically isolated syndrome, relapsing-remitting disease and active secondary progressive disease. In addition, it has a number of drugs and/or additional indications for current products in development, including Bysanti, Tradipitant, Imsidolimab, VTR-297, VQW-765, and others. Bysanti is the active metabolite of Fanapt.
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Events Timeline

(ET)
2026-03-03
16:40:00
AnaptysBio Plans Spin-Off of Biopharma Operations in Q2 2026
select
2026-03-03
08:10:00
Vanda Pharmaceuticals Granted FDA Hearing Approval
select
2026-02-25 (ET)
2026-02-25
07:30:00
Vanda Pharmaceuticals' Imsidolimab FDA Filing Accepted, Target Date December 12
select
2026-02-23 (ET)
2026-02-23
16:30:00
Major Averages Drop Over 1% Due to Tariff Policy
select
2026-02-23
12:00:00
Major Averages Drop Over 1% Due to Tariff Policy
select
2026-02-23
08:50:00
Significant Increases in Borrow Rates for Liquid Options
select

News

Benzinga
4.0
03-05Benzinga
Wall Street Analysts Adjust Ratings
  • Analyst Rating Changes: Top Wall Street analysts have adjusted their ratings on several companies, including upgrades, downgrades, and initiations, reflecting varying market perspectives on these firms.
  • EQIX Stock Outlook: Analysts' views on EQIX stock indicate a cautious market sentiment regarding its future performance, although specific ratings were not detailed in the report.
  • Market Dynamics Overview: Changes in analyst ratings can significantly influence investor decisions, potentially leading to stock price volatility, prompting investors to closely monitor these developments.
  • Access More Information: A complete view of all analyst rating changes can be found on Benzinga's analyst ratings page, providing comprehensive market insights and investment references.
seekingalpha
9.0
03-03seekingalpha
FDA Grants Hearing for Vanda's Hetlioz Jet Lag Drug
  • Hearing Approval: The FDA has granted a public hearing for Vanda Pharmaceuticals regarding its drug Hetlioz (tasimelteon) for jet lag, marking a rare occurrence for the agency and potentially the first in over four decades, indicating a significant scrutiny of the drug approval process.
  • Rejection Reasons: In January, the FDA declined to approve the additional indication for Hetlioz, stating that the data submitted did not adequately demonstrate efficacy, which poses challenges for Vanda's market prospects.
  • Current Approval Status: Hetlioz is currently approved for non-24-hour sleep-wake disorder and nighttime sleep disturbances associated with Smith-Magenis syndrome, showcasing its potential applications in specific areas.
  • Market Reaction: Despite the FDA's approval of the hearing, Vanda's stock fell approximately 4% on Tuesday, reflecting market uncertainty regarding the future development of its drug.
stocktwits
9.0
03-03stocktwits
FDA Grants Vanda Hearing on Jet Lag Drug Rejection
  • Hearing Approval: On March 2, 2026, the FDA approved Vanda's request for a formal hearing to review the proposed rejection of its supplemental new drug application for Hetlioz for jet lag treatment, marking the first such hearing in over 40 years, which could influence future approval processes.
  • Clinical Trial Results: While the FDA acknowledged positive results from Vanda's recent clinical trials, it expressed concerns that the controlled phase-advance protocols used in the studies do not adequately replicate real-world flight conditions, potentially impacting the drug's practical application.
  • Historical Rejection Background: Vanda's application for the jet lag indication was first rejected by the FDA in 2019, and a court-ordered re-review in August 2025 criticized the FDA for not adequately engaging with Vanda's evidence, highlighting the complexities and challenges in drug approvals.
  • Market Reaction: Retail sentiment around VNDA stock on Stocktwits remained neutral over the past 24 hours, with message volume decreasing from high to low levels, although VNDA stock has gained 66% over the past 12 months, indicating cautious optimism in the market regarding the company's future prospects.
PRnewswire
9.0
03-03PRnewswire
FDA Grants Vanda Hearing on HETLIOZ® Jet Lag Application
  • Hearing Approval: The FDA confirmed on March 2, 2026, that it will hold a formal evidentiary hearing to review Vanda's supplemental new drug application (sNDA) refusal for HETLIOZ®, a rare decision in over 40 years, highlighting the FDA's acknowledgment of the legal and scientific issues raised by Vanda.
  • Legal Victory: Vanda successfully overturned the FDA's refusal of HETLIOZ® in August 2025, with the court ruling that the FDA inadequately considered Vanda's clinical trial evidence, emphasizing the company's seven-year effort for a fair review process, which could lead to greater transparency in future drug approvals.
  • Market Potential: Currently approved for Non-24-Hour Sleep-Wake Disorder, if the sNDA is approved, HETLIOZ® would become the first FDA-approved treatment for jet lag disorder, addressing the needs of millions of travelers worldwide and presenting significant market expansion opportunities.
  • Company Vision: Vanda is focused on developing innovative therapies to meet high unmet medical needs, and the progress of this hearing not only recognizes the company's efforts but may also propel its further development in the biopharmaceutical sector, enhancing its position in the industry.
Newsfilter
9.0
03-03Newsfilter
FDA Grants Vanda Hearing on HETLIOZ® Jet Lag Application
  • Hearing Approval: The FDA confirmed on March 2, 2026, that it will hold a formal evidentiary hearing to review Vanda's supplemental new drug application (sNDA) refusal for HETLIOZ®, marking the first such hearing in over 40 years and highlighting the FDA's acknowledgment of Vanda's scientific evidence.
  • Legal Victory: Vanda successfully challenged the FDA's refusal in August 2025, with the court ruling that the FDA inadequately considered Vanda's clinical trial data, mandating a re-evaluation of the sNDA, reflecting Vanda's commitment to advocating for scientific fairness.
  • Market Potential: Currently approved for Non-24-Hour Sleep-Wake Disorder, HETLIOZ® could address a significant unmet need for millions of travelers suffering from jet lag if the sNDA is approved, indicating substantial market demand and commercial opportunity.
  • Transparency Enhancement: This hearing represents not only a procedural victory for Vanda but also a significant reform in the FDA's drug approval process, potentially influencing future standards and procedures, thereby enhancing industry trust.
PRnewswire
1.0
02-26PRnewswire
Vanda Pharmaceuticals to Participate in 2026 Citizens Life Sciences Conference
  • Conference Participation: Vanda Pharmaceuticals announced its participation in the 2026 Citizens Life Sciences Conference in Miami on March 11, 2026, with a corporate presentation scheduled for 2:15 p.m. Eastern Time, highlighting its latest advancements in the biopharmaceutical sector.
  • Online Access Convenience: Investors can access the conference presentation live on Vanda's corporate website, with a recommendation to register and download necessary software at least 15 minutes early, reflecting the company's commitment to investor communication.
  • Post-Conference Availability: An archived link to the conference will be available for approximately 30 days after the event, aimed at providing information to investors who could not attend live, thereby enhancing transparency.
  • Company Background: Vanda Pharmaceuticals is a leading global biopharmaceutical company focused on developing and commercializing innovative therapies to address high unmet medical needs and improve patient lives, showcasing its significant position in the industry.
Wall Street analysts forecast VNDA stock price to rise
4 Analyst Rating
Wall Street analysts forecast VNDA stock price to rise
3 Buy
1 Hold
0 Sell
Strong Buy
Current: 0.000
sliders
Low
7.50
Averages
13.63
High
22.00
Current: 0.000
sliders
Low
7.50
Averages
13.63
High
22.00
Truist
Buy
initiated
$18
AI Analysis
2026-03-05
Reason
Truist
Price Target
$18
AI Analysis
2026-03-05
initiated
Buy
Reason
Truist initiated coverage of Vanda Pharmaceuticals with a Buy rating and $18 price target. With three commercial drugs commanding $200M in sales plus "a slew of higher value near-commercial-ready assets nearing launch," the firm sees Vanda's reformulation of lead asset Fanapt launching with improved economics into a competitive schizophrenia and bipolar market differentiated by lower weight gain risk. "More interestingly" is Vanda's first-mover advantage of Nereus into adjunct therapy for GLP-1 induced vomiting, as the firm sees this as a derisked $1B opportunity.
B. Riley
Buy
maintain
$14 -> $17
2026-02-25
Reason
B. Riley
Price Target
$14 -> $17
2026-02-25
maintain
Buy
Reason
B. Riley raised the firm's price target on Vanda Pharmaceuticals to $17 from $14 and keeps a Buy rating on the shares. Following BYSANTI's approval, the firm's revenue model for Vanda has been updated, reflecting expected growth in the psychiatry franchise with peak BYSANTI sales now included and probability adjustments removed, the analyst tells investors in a research note. Base assumptions include mid-to-high single-digit quarter over quarter growth in BYSANTI/FANAPT prescriptions through 2026, the firm says.
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Valuation Metrics

The current forward P/E ratio for Vanda Pharmaceuticals Inc (VNDA.O) is -3.33, compared to its 5-year average forward P/E of -21.19. For a more detailed relative valuation and DCF analysis to assess Vanda Pharmaceuticals Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-21.19
Current PE
-3.33
Overvalued PE
157.78
Undervalued PE
-200.16

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
4.54
Current EV/EBITDA
0.00
Overvalued EV/EBITDA
11.20
Undervalued EV/EBITDA
-2.12

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
1.91
Current PS
1.90
Overvalued PS
2.72
Undervalued PS
1.11

Financials

AI Analysis
Annual
Quarterly

Whales Holding VNDA

T
Tang Capital Management, LLC
Holding
VNDA
+3.59%
3M Return

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Frequently Asked Questions

What is Vanda Pharmaceuticals Inc (VNDA) stock price today?

The current price of VNDA is 9.56 USD — it has increased 10.14

What is Vanda Pharmaceuticals Inc (VNDA)'s business?

Vanda Pharmaceuticals Inc. is a global biopharmaceutical company focused on the development and commercialization of therapies to address unmet medical needs and improve the lives of patients. The Company’s commercial portfolio consist of three products: Fanapt for the acute treatment of manic or mixed episodes associated with bipolar I disorder and the treatment of schizophrenia, HETLIOZ for the treatment of Non-24-Hour Sleep-Wake Disorder (Non-24) and for the treatment of nighttime sleep disturbances in Smith-Magenis syndrome (SMS) and PONVORY for the treatment of relapsing forms of multiple sclerosis (RMS), including clinically isolated syndrome, relapsing-remitting disease and active secondary progressive disease. In addition, it has a number of drugs and/or additional indications for current products in development, including Bysanti, Tradipitant, Imsidolimab, VTR-297, VQW-765, and others. Bysanti is the active metabolite of Fanapt.

What is the price predicton of VNDA Stock?

Wall Street analysts forecast VNDA stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for VNDA is13.63 USD with a low forecast of 7.50 USD and a high forecast of 22.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Vanda Pharmaceuticals Inc (VNDA)'s revenue for the last quarter?

Vanda Pharmaceuticals Inc revenue for the last quarter amounts to 57.22M USD, increased 7.58

What is Vanda Pharmaceuticals Inc (VNDA)'s earnings per share (EPS) for the last quarter?

Vanda Pharmaceuticals Inc. EPS for the last quarter amounts to -2.39 USD, increased 2887.50

How many employees does Vanda Pharmaceuticals Inc (VNDA). have?

Vanda Pharmaceuticals Inc (VNDA) has 533 emplpoyees as of March 11 2026.

What is Vanda Pharmaceuticals Inc (VNDA) market cap?

Today VNDA has the market capitalization of 565.07M USD.