Loading quotes...
Forecast
The analysts' average price target is €13.91 (+299.71%). The median is €13.91 (+299.71%).
| Buy |
Â
13 |
| Hold |
Â
5 |
| Sell |
Â
1 |
News Go to news feed
Vanda Pharmaceuticals unveils psychiatry growth plan focused on BYSANTI and NEREUS
At the Cantor conference, Vanda presented a growth strategy that expands its commercial portfolio from three to five products and identifies the psychiatry division as the main driver. Management targets a psychiatry revenue potential of $750 million by 2030, assuming approvals, switching rates and payer behavior proceed as planned. Near-term catalysts are BYSANTI (expected improved gross-to-net profile) and the launch of NEREUS with an additional opportunity related to GLP-1‑induced nausea; multiple Phase III readouts are expected in late 2026 to H1 2027. Remaining risks include regulatory hurdles, trial results and reimbursement dynamics. » More on de.investing.com
EU grants Vanda orphan drug status for imsidolimab in generalized pustular psoriasis
The European Commission has granted orphan drug status to Vanda’s investigational treatment imsidolimab for generalized pustular psoriasis (GPP), based on a recommendation from the EMA’s committee for rare diseases. It is the first agent to receive this designation for GPP in the EU; the FDA and Japan had previously awarded orphan status. The FDA is currently reviewing the biologics license application for imsidolimab, with a target decision date of December 12, 2026. Vanda holds an exclusive worldwide license; regulatory and patent exclusivity are expected into the late 2030s, along with benefits such as scientific advice, reduced fees, and market exclusivity. » More on de.investing.com
Vanda misses Q2 forecasts and reports significantly higher loss
Vanda reported an adjusted loss of $1.04 per share in the second quarter versus the $0.60 expected and revenue of $50.5 million (expectation $61.8 million). Strong prescription growth for Fanapt and moderate growth for PONVORY could not offset a sharp decline in HETLIOZ due to generic competition. Operating expenses rose markedly, the net loss widened to $62.5 million, and cash on hand stood at $170 million as of June 30. Vanda reconfirmed its full-year revenue guidance of $240–290 million, expects costs to decline from late 2026/2027, and pointed to several upcoming Phase III milestones and a PDUFA date in December 2026. » More on de.investing.com
Financials
| (EUR) | June 2026 | YoY |
|---|---|---|
| Revenue | 44.27M | 0.77% |
| Gross profit | 41.15M | 0.84% |
| Net profit | -54.77M | 137.29% |
| EBITDA | -53.91M | 93.33% |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €216.54M |
Number of shares | 60.46M |
52-week high/low | €8.92 - €3.48 |
| Dividends | No |
Beta | 0.69 |
P/E ratio | -0.86 |
PEG ratio | 0.01 |
P/B ratio | 1.09 |
P/S ratio | 1.12 |
Company profile
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.
| Name | Vanda Pharmaceuticals |
| CEO | Mihael H. Polymeropoulos |
| Headquarters | Washington,
dc USA |
| Website | |
| Sector | Materials |
| Industry | Chemicals |
| IPO | 04/12/2006 |
| Employees | 533 |
Ticker symbols
| Exchange | Symbol |
|---|---|
NASDAQ | VNDA |
Frankfurt | VM4.F |
DĂĽsseldorf | VM4.DU |
London | 0LKB.L |
SIX | VM4.SW |