Vanda Pharmaceuticals Inc.

Vanda Pharmaceuticals Inc.

VNDA
Vanda Pharmaceuticals Inc.US flagNASDAQ Global Market
5.95
USD
-0.05
- -
357.81MMarket Cap
2013 Y
2014 Y
2015 Y
2016 Y
2017 Y
2018 Y
2019 Y
2020 Y
2021 Y
2022 Y
2023 Y
2024 Y
2025 Y
TTM
Revenue per Share
1.12
1.44
2.6
3.36
3.69
3.8
4.28
4.56
4.84
4.51
3.36
3.42
3.67
3.68
Basic EPS, GAAP
-0.69
0.58
-0.94
-0.41
-0.35
0.5
2.17
0.43
0.6
0.11
0.04
-0.33
-3.74
-4.05
Free Cash Flow per Basic Share
-1.31
-2.6
0.23
-0.22
-0.08
0.09
0.85
0.92
1.15
0.55
0.22
-0.28
-1.87
-2.32
Dividend per Share
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Book Value per Share
-10.15
-8.28
-7.76
-7.96
-8.08
-6.61
-4.15
-3.62
-2.95
-2.8
-2.71
-3
-6.7
-7.49
Tangible Book Value per Share
1.29
3.86
2.23
2.38
2.35
4.93
7.3
7.93
8.73
9.01
7.38
7.3
3.57
2.8
Basic Weighted Avg Shares
30
35
42
43
45
51
53
54
56
56
57
58
59
59
Sales/Revenue/Turnover
34
50
110
146
165
193
227
248
269
254
193
199
216
218
Operating Margin (%)
-62.58
-114.75
-36.56
-12.72
-10.24
11.26
10.04
10.98
15.69
2.49
-7.24
-20.46
-69.95
-73.64
Depreciation Expense
2
3
14
12
3
3
3
3
3
3
4
10
12
13
Net Income, GAAP
-21
20
-40
-18
-16
25
116
23
33
6
3
-19
-220
-240
Effective Tax Rate (%)
- -
- -
- -
- -
- -
0.54
- -
26.28
21.74
44.47
60.42
- -
- -
- -
Profit Margin (%)
-62.15
40.25
-36.27
-12.33
-9.43
13.05
50.86
9.4
12.34
2.47
1.3
-9.51
-102.02
-109.99
Working Capital
103
134
115
124
99
246
295
343
404
428
345
339
202
158
LT Debt
- -
- -
- -
- -
- -
- -
12
11
10
9
7
8
7
7
Total Equity
44
161
133
131
131
275
411
453
505
527
545
539
327
281
Return on Invested Capital (%)
- -
-56.17
- -
- -
- -
10.63
- -
4.5
6.71
0.67
-1.01
- -
- -
- -
Return on Capital (%)
- -
-6.77
- -
- -
- -
-7.23
- -
-11.98
-19.77
-4.2
-1.71
- -
- -
- -
Return on Common Equity (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -

Capital Structure

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
ST Debt
5
6
6
LT Borrowings
- -
- -
- -
LT Finance Leases
6
7
7
Preferred Equity and Hybrid Capital
- -
- -
- -
Shares Outstanding
59
59
60
Market Capitalization
293
520
409

Working Capital

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
Total Current Assets
367
347
293
Cash, Cash Equivalents & STI
294
264
202
Accounts Receivable, Net
51
55
57
Inventories
2
2
2
Total Current Liabilities
118
145
136
Payables & Accruals
34
52
48
ST Debt
5
6
6
Deferred Revenue
- -
- -
- -

Growth Rates

FRC

in mil. unless spec.

(avg. rate of change)

10 years
5 years
1 year
Total Equity
14.67%
-4.25%
-39.25%
Free Cash Flow
66.52%
53.03%
579.76%
Net Income, GAAP
6.25%
22.84%
1,066.53%
Sales/Revenue/Turnover
8.03%
-1.88%
8.72%
Total Cash Common Dividend
- -
- -
- -

Quarterly Revenue

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
47
50
48
53
199
2025
50
53
56
57
216
2026
52
- -
- -
- -
- -

Quarterly Earnings Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
-0.07
-0.08
-0.09
-0.08
-0.33
2025
-0.5
-0.46
-0.38
-2.39
-3.74
2026
-0.82
- -
- -
- -
- -

Quarterly Dividends Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Company Description

APIChatGPT
CEO
Mihael H. Polymeropoulos
Full Time Employees
368
Sector
Healthcare
Industry
Biotechnology
Address
2200 Pennsylvania Avenue NW Washington DC United States of America 20037
IPO Date
Apr 12, 2006
Business
Vanda Pharmaceuticals Inc. (Nasdaq: VNDA) develops and commercializes innovative biopharmaceutical therapies focused on addressing high unmet medical needs in central nervous system disorders, sleep-wake conditions, psychiatric illnesses, and inflammatory diseases worldwide; the company, founded in 2003 and headquartered in Washington, DC, markets HETLIOZ (tasimelteon) for non-24-hour sleep-wake disorder and Smith-Magenis syndrome-associated nighttime sleep disturbances, including the LQ oral suspension formulation; Fanapt (iloperidone) for schizophrenia and acute bipolar I disorder, with a long-acting injectable formulation in development; and PONVORY (ponesimod) for multiple sclerosis, pursuing indications in psoriasis and ulcerative colitis with investigational new drug applications accepted by the FDA. Its pipeline encompasses tradipitant (VLY-686), a neurokinin-1 receptor antagonist for gastroparesis, motion sickness, and atopic dermatitis; Bysanti (milsaperidone) for bipolar I disorder, schizophrenia, and major depressive disorder; imsidolimab, licensed from AnaptysBio in February 2025 for generalized pustular psoriasis and potential expansion into other IL-36-related inflammatory conditions; VSJ-110 for dry eye; VPO-227 for secretory diarrhea disorders including cholera; VTR-297 for hematologic malignancies and onychomycosis; VQW-765 for social/performance anxiety; and VGT-1849B, which received FDA orphan drug designation for polycythemia vera, among others. Vanda operates globally with a subsidiary in the United Kingdom and targets rare diseases, neurology, psychiatry, and immunology patient populations through specialized sales forces and marketing campaigns. Recent developments include the $100 million acquisition of PONVORY from Johnson & Johnson, enabling commercial launch in the multiple sclerosis market and new indication pursuits; FDA approval and commercial rollout of Fanapt for acute bipolar I disorder; a global licensing agreement with AnaptysBio for imsidolimab development and commercialization; positive clinical results for tradipitant in preventing GLP-1 induced nausea and vomiting; a collaborative framework with the FDA to resolve disputes; and unsolicited acquisition proposals from Future Pak and Cycle Pharmaceuticals in 2024, which the company reviewed but did not pursue, reflecting ongoing strategic interest amid robust revenue growth to $267.7 million in 2024.

Company News

APIChatGPT
  • Vanda Pharmaceuticals Announces Orphan Drug Designation in Japan for Imsidolimab in Generalized Pustular Psoriasis

  • Vanda: A Long-Term Pharma Growth Idea, Despite Q1 Earnings Miss

  • Vanda Pharmaceuticals Announces Participation at May 2026 Investor Conferences

  • Vanda Pharmaceuticals Inc. (VNDA) Q1 2026 Earnings Call Transcript

  • Vanda Pharmaceuticals (VNDA) Reports Q1 Loss, Lags Revenue Estimates

  • Vanda Pharmaceuticals Reports First Quarter 2026 Financial Results

  • Wall Street Analysts Predict a 105.03% Upside in Vanda (VNDA): Here's What You Should Know

  • Vanda Pharmaceuticals Announces U.S. Commercial Availability of NEREUS™ (tradipitant), the First New Pharmacologic Treatment for People with Motion Sickness in More Than 40 Years

  • Vanda Pharmaceuticals Announces U.S. Commercial Availability of NEREUS™ (tradipitant), the First New Pharmacologic Treatment for People with Motion Sickness in More Than 40 Years

  • Vanda Pharmaceuticals to Announce First Quarter 2026 Financial Results on May 6, 2026

  • Vanda Pharmaceuticals announces the publication of "Efficacy and Safety of Imsidolimab for Generalized Pustular Psoriasis" in NEJM Evidence

  • Incyte (INCY) Beats Q1 Earnings and Revenue Estimates

  • Vanda Pharmaceuticals Appoints Dr. Charles Duncan to its Board of Directors

  • Vanda Pharmaceuticals (NASDAQ:VNDA) Stock Passes Above 200-Day Moving Average – Time to Sell?

  • Vanda Pharmaceuticals Inc. (NASDAQ:VNDA) Sees Significant Increase in Short Interest

  • Contrasting Vanda Pharmaceuticals (NASDAQ:VNDA) and Atrinsic (NASDAQ:PTIX)

  • Vanda Pharmaceuticals Calls on FDA to Withdraw Proposal from FY 2027 Legislative Agenda That Would Extend Drug Review Timelines

  • Vanda Pharmaceuticals Announces Initiation of The Thetis Study, a Clinical Trial of NEREUS™ for the Prevention of Vomiting Induced by GLP-1 Receptor Agonists

  • Vanda Pharmaceuticals (NASDAQ:VNDA) Share Price Passes Above 200-Day Moving Average – Should You Sell?

  • Vanda Pharmaceuticals Calls for Stronger FDA Action to Accelerate Shift from Animal Testing to Human-Relevant Methods