VNDA
NASDAQVanda Pharmaceuticals Inc.
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News · 26 weeks52-10%
2025-10-262026-04-19
Mix3590d
- Insider13(37%)
- SEC Filings10(29%)
- Other8(23%)
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- Analyst1(3%)
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Latest news
25 items- SECSEC Form DEFA14A filed by Vanda Pharmaceuticals Inc.DEFA14A - Vanda Pharmaceuticals Inc. (0001347178) (Filer)
- SECSEC Form DEF 14A filed by Vanda Pharmaceuticals Inc.DEF 14A - Vanda Pharmaceuticals Inc. (0001347178) (Filer)
- SECVanda Pharmaceuticals Inc. filed SEC Form 8-K: Leadership Update, Financial Statements and Exhibits8-K - Vanda Pharmaceuticals Inc. (0001347178) (Filer)
- PRVanda Pharmaceuticals Appoints Dr. Charles Duncan to its Board of DirectorsWASHINGTON, April 22, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ:VNDA) today announced the appointment of Charles Duncan, Ph.D. to its Board of Directors effective April 22, 2026. Following Dr. Duncan's appointment, Vanda's Board of Directors is now comprised of seven directors, six of whom are independent. Dr. Duncan is a highly experienced and respected leader in the life sciences and biotechnology sector," said Mihael H. Polymeropoulos, M.D., Vanda's President, CEO and Chairman of the Board. "We are excited to welcome him to our strong and independent Boa
- INSIDERSEC Form 3 filed by new insider Polymeropoulos Christos Vasilios Mihael3 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)
- INSIDERSEC Form 3 filed by new insider Howell Scott Laverne3 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)
- PRVanda Pharmaceuticals Calls on FDA to Withdraw Proposal from FY 2027 Legislative Agenda That Would Extend Drug Review TimelinesWASHINGTON, April 9, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ:VNDA) today highlighted a legislative proposal contained in the FDA's FY 2027 Congressional Budget Justification. The proposal would eliminate the simple statutory requirement that the FDA must review a new drug application (NDA) within 180 days of filing.In plain terms, this change would extend statutory review timelines rather than shorten them. It would replace the 180-day legal requirement with the longer Prescription Drug User Fee Act (PDUFA) and Generic Drug User Fee Amendments (GDUFA) per
- PRVanda Pharmaceuticals Announces Initiation of The Thetis Study, a Clinical Trial of NEREUS™ for the Prevention of Vomiting Induced by GLP-1 Receptor AgonistsWASHINGTON, April 8, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ:VNDA) today announced the initiation of Thetis, a clinical trial evaluating NEREUS™ (tradipitant) for the prevention of vomiting in patients receiving glucagon-like peptide-1 (GLP-1) receptor agonist therapies. NEREUS™ was recently approved for the prevention of vomiting induced by motion.1 GLP-1 receptor agonists, including semaglutide and tirzepatide, have transformed the treatment of type 2 diabetes and obesity. However, gastrointestinal side effects, particularly nausea and vomiting, remain
- SECVanda Pharmaceuticals Inc. filed SEC Form 8-K: Leadership Update8-K - Vanda Pharmaceuticals Inc. (0001347178) (Filer)
- SECAmendment: SEC Form SCHEDULE 13G/A filed by Vanda Pharmaceuticals Inc.SCHEDULE 13G/A - Vanda Pharmaceuticals Inc. (0001347178) (Subject)
- PRVanda Pharmaceuticals Calls for Stronger FDA Action to Accelerate Shift from Animal Testing to Human-Relevant MethodsWASHINGTON, March 19, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ:VNDA), a leader in innovative drug development and a vocal advocate for reducing unnecessary animal testing, today voiced serious concerns over the U.S. Food and Drug Administration (FDA)'s new draft guidance, "General Considerations for the Use of New Approach Methodologies in Drug Development," released March 18, 2026, by the Center for Drug Evaluation and Research (CDER). The FDA's draft guidance aims to support the use of New Approach Methodologies (NAMs)—advanced non-animal tools like in v
- SECVanda Pharmaceuticals Inc. filed SEC Form 8-K: Regulation FD Disclosure8-K - Vanda Pharmaceuticals Inc. (0001347178) (Filer)
- ANALYSTTruist initiated coverage on Vanda Pharma with a new price targetTruist initiated coverage of Vanda Pharma with a rating of Buy and set a new price target of $18.00
- INSIDERSVP & General Counsel Williams Timothy sold $350,755 worth of shares (42,434 units at $8.27), decreasing direct ownership by 10% to 377,450 units (SEC Form 4)4 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)
- INSIDERSVP, CFO & Treasurer Moran Kevin Patrick sold $350,821 worth of shares (42,442 units at $8.27), decreasing direct ownership by 9% to 411,380 units (SEC Form 4)4 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)
- INSIDERSVP, Chief Marketing Officer Wijkstrom Joakim sold $254,590 worth of shares (30,800 units at $8.27), decreasing direct ownership by 8% to 333,469 units (SEC Form 4)4 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)
- INSIDERPresident and CEO Polymeropoulos Mihael Hristos sold $1,276,971 worth of shares (156,235 units at $8.17), decreasing direct ownership by 5% to 2,704,496 units (SEC Form 4)4 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)
- INSIDERSVP, Business Development Birznieks Gunther sold $350,730 worth of shares (42,431 units at $8.27), decreasing direct ownership by 8% to 494,197 units (SEC Form 4)4 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)
- PRVanda Announces FDA Grants Landmark Hearing for HETLIOZ® in Jet Lag Disorder, the First Drug Approval Hearing in Over 40 YearsWASHINGTON, March 3, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ:VNDA) today announced that the U.S. Food and Drug Administration (FDA) has granted the company's request for a formal evidentiary public hearing to review the Center for Drug Evaluation and Research's (CDER) proposal to refuse approval of Vanda's supplemental new drug application (sNDA) for HETLIOZ® (tasimelteon) in the treatment of jet lag disorder. The FDA confirmed the decision to grant a hearing in a letter from the Office of the Commissioner dated March 2, 2026. The hearing will proceed und
- PRVanda Pharmaceuticals Announces Participation in the 2026 Citizens Life Sciences ConferenceWASHINGTON, Feb. 26, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ:VNDA) today announced that the company will participate in the 2026 Citizens Life Sciences Conference in Miami on Wednesday, March 11, 2026. A corporate presentation is scheduled for 2:15 p.m. Eastern Time. The corporate presentation given at the Citizens Life Sciences Conference may be accessed live on Vanda's corporate website, www.vandapharma.com. Investors should click on the Investors tab and follow the link under Recent Events. Investors are advised to go to the conference website at least
- PRVanda Pharmaceuticals Announces FDA Acceptance of Biologics License Application Filing for Imsidolimab for the Treatment of Generalized Pustular PsoriasisWASHINGTON, Feb. 25, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ:VNDA) today announced that the U.S. Food and Drug Administration (FDA) has accepted the filing of its Biologics License Application (BLA) for imsidolimab for the treatment of Generalized Pustular Psoriasis (GPP), with a target action date of December 12, 2026. GPP is a rare, chronic, life-threatening autoinflammatory skin disorder characterized by sudden flares of widespread pustules, erythema, and systemic symptoms such as fever and fatigue. The pathogenesis of GPP is increasingly understood th
- INSIDERDirector Honore Tage sold $240,900 worth of shares (30,000 units at $8.03), decreasing direct ownership by 24% to 93,469 units (SEC Form 4)4 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)
- SECVanda Pharmaceuticals Inc. filed SEC Form 8-K: Other Events, Financial Statements and Exhibits8-K - Vanda Pharmaceuticals Inc. (0001347178) (Filer)
- PRVanda Pharmaceuticals Announces FDA Approval of BYSANTI™ (milsaperidone) for the treatment of Bipolar I Disorder and Schizophrenia - A New Chemical Entity Opening New Horizons in Psychiatric InnovationWASHINGTON, Feb. 20, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (NASDAQ:VNDA) today announced that the U.S. Food and Drug Administration (FDA) has approved BYSANTI™ (milsaperidone) tablets, a first line therapy for the acute treatment of manic or mixed episodes associated with bipolar I disorder and for the treatment of schizophrenia in adults. BYSANTI™ is a new chemical entity (NCE) that belongs in the class of atypical antipsychotics. In clinical studies BYSANTI™ demonstrated bioequivalence to iloperidone across the therapeutic dosing spectrum enabling it to leverage well
- INSIDERSVP, Chief Marketing Officer Wijkstrom Joakim was granted 125,000 shares, increasing direct ownership by 52% to 364,269 units (SEC Form 4)4 - Vanda Pharmaceuticals Inc. (0001347178) (Issuer)