で公開中です! 詳しく見る
VNDAのアイコン

Vanda Pharmaceuticals

4.03 USD
-0.21
4.95%
終値時点 更新済み 10月16日 16:00 EDT
プレマーケット
時間外取引
4.02
-0.01
0.25%
1日
-4.95%
5日間
-11.62%
1か月
-19.4%
3か月
-26.06%
6か月
-43.72%
年初来
-51.15%
1年
-23.53%
5年間
-77.69%
10年間
-74.77%
 

概要: Vanda Pharmaceuticals Inc is a biopharmaceutical company engaged in the development and commercialization of therapies to address high unmet medical needs and improve the lives of patients. Its commercial portfolio comprises three products; HETLIOZ for the treatment of Non-24-Hour Sleep-Wake Disorder (Non-24) & nighttime sleep disturbances in Smith-Magenis Syndrome (SMS); Fanapt for the treatment of schizophrenia; and PONVORY. Its other products include ASO Molecules, VQW-765, Tradipitant, and VTR-297. The maximum of revenue is derived from the Fanapt product sales. Geographically, the company sells its product predominantly in the United States, and also in Israel, Europe, and Canada.

従業員数: 533

ニュース

ポジティブ
ニュートラル
ネガティブ
センチメント 3か月間
ポジティブ 7.1%
ニュートラル 71.4%
ネガティブ 21.4%
ネガティブ
Benzinga
昨日
Vanda Pharmaceuticals Says Experimental Anxiety Treatment Misses Primary Endpoint
Vanda Pharmaceuticals Inc. (NASDAQ:VNDA) on Wednesday shared an update regarding its clinical development pipeline.
Vanda Pharmaceuticals Says Experimental Anxiety Treatment Misses Primary Endpoint
ネガティブ
Reuters
一昨日
Vanda says anxiety drug failed main goal of late-stage study, puts program on hold
Vanda Pharmaceuticals said on Wednesday its experimental drug for social anxiety disorder ​failed the main goal of a ‌late-stage study, prompting the company to put the program on hold pending further analysis of ​the data.
Vanda says anxiety drug failed main goal of late-stage study, puts program on hold
ニュートラル
PRNewsWire
一昨日
Vanda Pharmaceuticals Provides Update on VQW-765 Clinical Development Program
Phase III clinical study of VQW-765 in adults with social anxiety disorder did not meet its primary endpoint Consistent with prior studies, VQW-765 was safe and well tolerated WASHINGTON, Oct. 14, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today provided an update on its clinical development program for VQW-765, a novel small molecule alpha 7 nicotinic acetylcholine receptor (α7-nAChR) partial agonist. Vanda's Phase III clinical study, VP-VQW-765-3201 (Study 3201), which evaluated VQW-765 for the on-demand treatment of acute anxiety in adults with social anxiety disorder, did not meet its primary endpoint.
Vanda Pharmaceuticals Provides Update on VQW-765 Clinical Development Program
ニュートラル
PRNewsWire
14 日前
Vanda Pharmaceuticals Announces Presentation at 2026 EADV Annual Meeting
WASHINGTON, Oct. 2, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Nasdaq: VNDA) today announced participation at the European Academy of Dermatology and Venereology (EADV) Annual Meeting, being held in Vienna, Austria, from September 30 through October 3, 2026. The following will be presented: Presentation Title: "Rapid reduction in neutrophils and neutrophil percentage-to-albumin ratio upon treatment with imsidolimab in patients with GPP" Abstract ID: AS-4323 Poster Number: P1769 Presentation Title: "Immunogenicity of Imsidolimab for the Treatment of Generalized Pustular Psoriasis (GPP)" Abstract ID: AS-2420 Poster Number: P1784 Presentation Title: "Imsidolimab Improves Generalized Pustular Psoriasis (GPP) Pustulation as Measured by the Pustulation Rating Scale (PRS): Results from the GEMINI-1 Study" Abstract ID: AS-2421 Poster Number: P2806 About Imsidolimab Imsidolimab is a fully humanized IgG4 monoclonal antibody that inhibits IL-36 receptor signaling and is being developed for GPP, a rare orphan indication.
Vanda Pharmaceuticals Announces Presentation at 2026 EADV Annual Meeting
ニュートラル
PRNewsWire
17 日前
Vanda Pharmaceuticals Announces Positive Phase III Results for HETLIOZ®(tasimelteon) in Delayed Sleep-Wake Phase Disorder
Study met its primary endpoint: timing of sleep onset shifted 37.1 minutes earlier versus placebo (p=0.022) 60% of HETLIOZ ® treated participants shifted sleep at least 30 minutes earlier, compared to 15% of the placebo arm WASHINGTON, Sept. 29, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Nasdaq: VNDA) today announced positive topline results from its pivotal Phase III study of HETLIOZ® (tasimelteon) 20 mg in adults with Delayed Sleep-Wake Phase Disorder (DSWPD).
Vanda Pharmaceuticals Announces Positive Phase III Results for HETLIOZ®(tasimelteon) in Delayed Sleep-Wake Phase Disorder
ニュートラル
PRNewsWire
先月
Vanda Pharmaceuticals Announces Participation at September 2026 Investor Conferences
WASHINGTON, Sept. 2, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today announced that the company will participate at the following upcoming investor conferences in September 2026: The Wells Fargo 21st Annual Healthcare Conference in Boston on Tuesday, September 8, 2026.
Vanda Pharmaceuticals Announces Participation at September 2026 Investor Conferences
ニュートラル
PRNewsWire
先月
Vanda Pharmaceuticals Granted Orphan Designation for Imsidolimab for the Treatment of Generalized Pustular Psoriasis by the European Commission
WASHINGTON, Aug. 24, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today announced that its investigational drug imsidolimab has received Orphan Designation from the European Commission, based on the positive opinion received from the European Medicines Agency's (EMA) Committee for Orphan Medicinal Products (COMP), for the treatment of Generalized Pustular Psoriasis (GPP), which is a severe, chronic, and potentially life-threatening inflammatory skin disease driven by dysregulation in the interleukin-36 (IL-36) signaling pathway.1 The US Food and Drug Administration (FDA) and Japan's Ministry of Health, Labour and Welfare have previously granted Orphan Drug Designation to imsidolimab for the treatment of GPP. This marks the first time the European Commission has granted orphan designation recognition for a drug to treat GPP in the European Union (EU).
Vanda Pharmaceuticals Granted Orphan Designation for Imsidolimab for the Treatment of Generalized Pustular Psoriasis by the European Commission
ニュートラル
PRNewsWire
先月
NEREUS™ Sponsored No. 47 IndyCar Ready for Historic Freedom 250 Grand Prix in Washington, D.C.
WASHINGTON, Aug. 22, 2026 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Nasdaq: VNDA) today announced that the NEREUS™ branded No. 47 entry from Rahal Letterman Lanigan Racing, driven by Mick Schumacher, is set to compete this weekend in the inaugural Freedom 250 Grand Prix of Washington, D.C.
NEREUS™ Sponsored No. 47 IndyCar Ready for Historic Freedom 250 Grand Prix in Washington, D.C.
ポジティブ
Zacks Investment Research
2 か月前
4 Psoriasis Drug Stocks to Watch During Psoriasis Awareness Month 2026
PTGX, ALMS, ORKA and VNDA offer diverse psoriasis opportunities, spanning approved therapies, late-stage candidates and earlier-stage programs.
4 Psoriasis Drug Stocks to Watch During Psoriasis Awareness Month 2026
ニュートラル
Seeking Alpha
2 か月前
Vanda Pharmaceuticals Inc. (VNDA) Q2 2026 Earnings Call Transcript
Vanda Pharmaceuticals Inc. (VNDA) Q2 2026 Earnings Call Transcript
Vanda Pharmaceuticals Inc. (VNDA) Q2 2026 Earnings Call Transcript
価格チャートは Lightweight Charts™ を使用して実装されています