VNDA Stock - Vanda Pharmaceuticals Inc.
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Financial Statements
| Metric | FY2024 | FY2023 | FY2022 | FY2021 | FY2020 |
|---|---|---|---|---|---|
| Revenue | $198.77M | $192.64M | $254.38M | $268.68M | $248.17M |
| Gross Profit | $187.46M | $177.84M | $230.10M | $243.05M | $224.80M |
| Gross Margin | 94.3% | 92.3% | 90.5% | 90.5% | 90.6% |
| Operating Income | $-40,660,000 | $-13,952,000 | $6.33M | $42.16M | $27.24M |
| Net Income | $-18,900,000 | $2.51M | $6.28M | $33.15M | $23.34M |
| Net Margin | -9.5% | 1.3% | 2.5% | 12.3% | 9.4% |
| EPS | $-0.32 | $0.04 | $0.11 | $0.60 | $0.43 |
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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Price Targets
Recent Analyst Actions
| Date | Firm | Action | Rating | Price Target |
|---|---|---|---|---|
| November 5th 2025 | B. Riley Securities | Initiation | Buy | $11 |
| October 31st 2024 | H.C. Wainwright | Initiation | Buy | $18 |
| July 11th 2024 | Cantor Fitzgerald | Initiation | Overweight | $11 |
Earnings History & Surprises
VNDAEPS Surprise History
Quarterly EPS Details
| Period | Report Date | Estimated EPS | Actual EPS | Surprise | Result |
|---|---|---|---|---|---|
Q2 2026 | May 5, 2026 | — | — | — | — |
Q1 2026 | Feb 12, 2026 | $-1.45 | — | — | — |
Q4 2025 | Oct 29, 2025 | $-0.31 | $-0.38 | -22.6% | ✗ MISS |
Q3 2025 | Jul 31, 2025 | $-0.34 | $-0.46 | -35.3% | ✗ MISS |
Q2 2025 | May 7, 2025 | $-0.55 | $-0.50 | +9.1% | ✓ BEAT |
Q1 2025 | Feb 13, 2025 | $-0.14 | $-0.08 | +42.9% | ✓ BEAT |
Q4 2024 | Nov 6, 2024 | $-0.17 | $-0.09 | +47.1% | ✓ BEAT |
Q3 2024 | Jul 31, 2024 | $-0.21 | $-0.08 | +61.9% | ✓ BEAT |
Q2 2024 | May 8, 2024 | $0.05 | $-0.07 | -240.0% | ✗ MISS |
Q1 2024 | Feb 7, 2024 | $-0.09 | $-0.04 | +55.6% | ✓ BEAT |
Q4 2023 | Nov 8, 2023 | $0.00 | $0.00 | +100.0% | ✓ BEAT |
Q3 2023 | Jul 27, 2023 | $-0.13 | $0.03 | +123.1% | ✓ BEAT |
Q2 2023 | May 3, 2023 | — | $0.06 | — | — |
Q1 2023 | Feb 8, 2023 | $0.08 | $0.12 | +50.0% | ✓ BEAT |
Q4 2022 | Nov 2, 2022 | $0.09 | $0.06 | -33.3% | ✗ MISS |
Q3 2022 | Aug 3, 2022 | $0.11 | $0.05 | -54.5% | ✗ MISS |
Q2 2022 | May 5, 2022 | $-0.01 | $-0.11 | -1000.0% | ✗ MISS |
Q1 2022 | Feb 23, 2022 | $0.09 | $0.12 | +33.3% | ✓ BEAT |
Q4 2021 | Nov 3, 2021 | $0.18 | $0.14 | -22.2% | ✗ MISS |
Q3 2021 | Jul 28, 2021 | $0.14 | $0.17 | +21.4% | ✓ BEAT |
Latest News
Vanda Pharmaceuticals Submitted An FDA Biologics License Application For Imsidolimab For Generalized Pustular Psoriasis
📈 PositiveMarket-Moving News for December 5th
➖ NeutralVanda jumps as FDA lifts tradipitant partial clinical hold
📈 PositiveVanda Pharmaceuticals shares are trading higher after the company announced that the FDA lifted its partial clinical hold on protocol VP-VLY-686-3403.
📈 PositiveVanda Pharma Announces FDA Has Lifted The Partial Hold On Tradipitant, Clearing Path For Expanded Motion-Sickness Studies Ahead Of Dec. 30 PDUFA Date
📈 PositiveVanda Pharmaceuticals Says FDA Extends Tradipitant Partial Clinical Hold Re-Review To December 5 2025 As Motion Sickness NDA Review And Labeling Discussions Continue Toward December 30 2025 PDUFA Date
➖ NeutralHC Wainwright & Co. Reiterates Buy on Vanda Pharmaceuticals, Maintains $20 Price Target
📈 PositiveVanda Pharmaceuticals Option Alert: Dec 19 $6 Calls At The Ask: 2499 @ $0.4 Vs 572 OI; Ref=$5.295
📈 PositiveVanda Pharmaceuticals shares are trading higher after the company reported that tradipitant lowered GLP 1 induced nausea and vomiting in adult participants.
📈 PositiveReported Earlier, Vanda Reports Tradipitant Significantly Reduces GLP 1 Induced Nausea And Vomiting Strengthening Role As Adjunct In Rapidly Expanding $50B Plus Market
📈 PositiveB. Riley Securities Initiates Coverage On Vanda Pharmaceuticals with Buy Rating, Announces Price Target of $11
📈 PositiveVanda Pharmaceuticals shares are trading lower. Cantor Fitzgerald lowered its price target on the stock from $13 to $11.
📉 NegativeCantor Fitzgerald Maintains Overweight on Vanda Pharmaceuticals, Lowers Price Target to $11
➖ NeutralVanda Pharmaceuticals shares are trading lower after the company reported mixed Q3 financial results and narrowed its FY25 sales guidance.
📉 NegativeVanda Pharmaceuticals Narrows FY2025 Sales Guidance from $210.000M-$250.000M to $210.000M-$230.000M vs $224.977M Est
📉 NegativeVanda Pharma Q3 EPS $(0.38) Beats $(0.45) Estimate, Sales $56.258M Miss $58.733M Estimate
➖ NeutralVanda Pharmaceuticals Agrees On A Collaborative Framework With The FDA For The Resolution Of Certain Disputes Regarding Hetlioz And Tradipitant
📈 PositiveVanda Pharmaceuticals Announced The Publication Of An Article Titled "Melatonin Agonist Tasimelteon Improves Sleep In Patients With Primary Insomnia: A Multicenter, Randomized, Double-blind, Placebo-Controlled Trial" In PLOS One, A Leading Open-Access Journal
📈 PositiveVanda Pharmaceuticals Receives FDA Orphan Drug Designation For VGT-1849B A Peptide Nucleic Acid-Based Candidate In Polycythemia Vera
📈 PositiveVanda Pharmaceuticals Asked Martin Makary To Review The Decision Made By Jacqueline Corrigan-Curay, The Departing Director Of The FDA's Center For Drug Evaluation And Research Days Before Her Retirement That Upholds An Office Of Generic Drugs Decision To Approve Two Generic Versions Of Hetlioz
📉 NegativeFrequently Asked Questions about VNDA
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