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Vanda Pharmaceuticals

5.12

+0.07501.49%

Volume:221.90K

Turnover:1.13M

Market Cap:309.27M

PE:-1.10

High:5.15

Open:5.10

Low:5.05

Close:5.04

52wk High:9.94

52wk Low:4.27

Shares:60.46M

Float Shares:47.66M

Volume Ratio:0.67

T/O Rate:0.47%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-4.6291

EPS(LYR):-3.7413

ROE:-77.81%

ROA:-22.38%

PB:1.40

PE(LYR):-1.37

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Overview Company News Filings

Vanda Pharmaceuticals Inc - Proposal Would Eliminate FDA 180-Day Nda Review Requirement

THOMSON REUTERS

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

THOMSON REUTERS

Vanda Pharmaceuticals: Undervalued GLP-1 Adjunct Opportunity Driven by Tradipitant’s Pivotal Thetis Trial

Vanda starts Thetis trial of NEREUS to curb GLP-1 therapy vomiting

Vanda Pharmaceuticals Announces Initiation of the Thetis Study, a Clinical Trial of Nereus™ for the Prevention of Vomiting Induced by Glp-1 Receptor Agonists

THOMSON REUTERS

Vanda Pharmaceuticals Inc - Topline Results From Thetis Study Expected by Q4 2026

THOMSON REUTERS

Vanda Pharmaceuticals Inc: Phase 2 Study Succeeded and Met Its Primary Endpoint

THOMSON REUTERS

Vanda SVP, General Counsel Timothy Williams resigns effective April 10

Ema's Chmp: Confirmed Recommendation to Refuse a Change to Marketing Authorisation for Hetlioz (Tasimelteon)

THOMSON REUTERS

Vanda Pharmaceuticals Calls for FDA Action to Accelerate Shift From Animal Testing to Human-Relevant Methods

THOMSON REUTERS

Vanda Pharmaceuticals urges FDA to revise draft guidance on non-animal testing methods

Ema: Refusal of Change to Hetlioz Marketing Authorisation to Add Treatment of Nighttime Sleep Disturbance in Adults With Smith-Magenis Syndrome

THOMSON REUTERS

Ema: Issued Its Opinion on Hetlioz Marketing Authorisation Change After Re-Examination on 16 March

THOMSON REUTERS

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