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VNDA Overview

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$
0.000
0.000(0.000%)
At close
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
6.891
Open
6.830
VWAP
6.70
Vol
1.17M
Mkt Cap
393.07M
Low
6.570
Amount
7.82M
EV/EBITDA(TTM)
--
Total Shares
59.11M
EV
152.07M
EV/OCF(TTM)
--
P/S(TTM)
1.88
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
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2026-03-03
08:10:00
Vanda Pharmaceuticals Granted FDA Hearing Approval
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2026-02-25 (ET)
2026-02-25
07:30:00
Vanda Pharmaceuticals' Imsidolimab FDA Filing Accepted, Target Date December 12
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2026-02-23 (ET)
2026-02-23
16:30:00
Major Averages Drop Over 1% Due to Tariff Policy
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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
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News

moomoo
9.0
03-27moomoo
EMA's CHMP Reaffirms Decision to Deny Change in Marketing Authorization for Hetlioz (Tasimelteon)
  • EMA's Recommendation: The European Medicines Agency (EMA) has confirmed its recommendation to reuse a specific change in the marketing authorization process.

  • Marketing Authorization: This recommendation pertains to the marketing authorization for a product associated with the organization Hetlioz, which is linked to the treatment of certain conditions.

PRnewswire
7.0
03-19PRnewswire
Vanda Pharmaceuticals Raises Concerns Over FDA's New Guidance on Drug Development
  • FDA Guidance Concerns: Vanda Pharmaceuticals expressed serious concerns regarding the FDA's draft guidance released on March 18, 2026, which aims to support New Approach Methodologies (NAMs) but fails to deliver the substantial reforms needed for a shift away from animal testing, potentially impacting drug development efficiency and ethical standards.
  • Ethics and Science Balance: While Vanda acknowledges the FDA's commitment to improving human predictivity and ethical standards, the draft guidance does not strike a better balance between regulatory caution and the scientific reforms necessary, which could delay patient access to safer drugs and affect Vanda's leadership in innovative drug development.
  • Legal Challenges to Animal Testing: Vanda has a proven track record of advocating for science-driven change, including legal challenges against FDA requirements for prolonged animal studies, such as nine-month dog toxicity tests, highlighting the ethical imperative to minimize animal suffering, particularly in dogs.
  • Collaboration and Policy Advocacy: Vanda stands ready to partner with the FDA, HHS, and stakeholders to advance regulatory policies that leverage cutting-edge science, protect patient safety, reduce animal suffering, and align with both ethical and scientific imperatives, aiming to accelerate the drug development process.
Newsfilter
7.0
03-19Newsfilter
Vanda Pharmaceuticals Raises Concerns Over FDA's New Draft Guidance
  • Draft Guidance Flaws: Vanda Pharmaceuticals expresses serious concerns regarding the FDA's draft guidance released on March 18, 2026, criticizing its lack of concrete non-animal testing alternatives, absence of real-world examples, and performance benchmarks, which could hinder the adoption of innovative tools and impact drug development efficiency and safety.
  • Insufficient Scientific Basis: The draft provides limited scientific references and practical examples of validated New Approach Methodologies (NAMs), failing to offer developers clear benchmarks for success, potentially leading to a lack of confidence in new methods and delaying drug market entry.
  • Balancing Ethics and Science: CEO Mihael H. Polymeropoulos emphasizes the need for the FDA to strike a better balance between regulatory caution and scientific reform to ensure patients gain faster access to safer drugs while addressing ethical concerns related to animal testing, particularly in dogs.
  • Call for Revision: Vanda urges the FDA to withdraw the current draft and substantially revise it with stronger scientific grounding and specific NAM examples to accelerate drug development and reduce animal suffering, ensuring the effectiveness and human relevance of new methods.
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.
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 -21.81. 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
-21.81
Current PE
-3.33
Overvalued PE
158.12
Undervalued PE
-201.74

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
4.45
Current EV/EBITDA
0.00
Overvalued EV/EBITDA
11.09
Undervalued EV/EBITDA
-2.19

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
1.90
Current PS
1.90
Overvalued PS
2.69
Undervalued PS
1.10

Financials

AI Analysis
Annual
Quarterly

Whales Holding VNDA

T
Tang Capital Management, LLC
Holding
VNDA
-5.24%
3M Return

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Frequently Asked Questions

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

The current price of VNDA is 6.65 USD — it has decreased -3.76

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 31 2026.

What is Vanda Pharmaceuticals Inc (VNDA) market cap?

Today VNDA has the market capitalization of 393.07M USD.