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Vanguard Health Care ETF

316.08

-3.7100-1.16%

Pre-market: 316.00-0.0800-0.03%08:19 EDT

Volume:231.18K

Turnover:73.56M

Market Cap:19.02B

PE:34.31

High:320.01

Open:319.37

Low:316.08

Close:319.79

52wk High:330.75

52wk Low:260.42

Shares:60.18M

Float Shares:60.18M

Volume Ratio:1.38

T/O Rate:0.38%

Dividend:4.61

Dividend Rate:1.46%

EPS(TTM):9.21

EPS(LYR):41.51

ROE:3.75%

ROA:0.89%

PB:0.96

PE(LYR):7.61

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Overview Company News Filings

Ain Holdings Responds to Supreme Court Ruling on Former Directors with Stronger Compliance Push

Eli Lilly's Olumiant Gets FDA Approval for Severe Alopecia Areata in Adolescents

MT Newswires Live

Talius strengthens sales leadership with healthcare tech executive hire

Nektar selloff on trial brings ‘strong entry point,’ says BTIG

Analysts Have Conflicting Sentiments on These Healthcare Companies: Roivant Sciences (ROIV) and Johnson & Johnson (JNJ)

US FDA Approves AbbVie's Drug for Parkinson's Disease

US FDA - Approves Juvmo (Tavapadon) for Parkinson’s Disease in Adults on Sept 25, 2026

THOMSON REUTERS

Ifinatamab Deruxtecan Biologics License Application for Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily Withdrawn

Perrigo Co. PLC Stock Outperforms Competitors on Strong Trading Day

Eli Lilly Gets Expanded Label Approval from FDA for Alopecia Drug

FDA Approves Lilly's Olumiant (Baricitinib) for Pediatric Patients 12 Years of Age and Older with Severe Alopecia Areata

THOMSON REUTERS

Merck, Daiichi Sankyo Withdraw US Application for Lung Cancer Drug

Merck, Daiichi Sankyo voluntarily withdraw BLA for ifinatamab deruxtecan

Merck & Co - Daiichi Sankyo and Merck Withdraw Bla for Ifinatamab Deruxtecan in Es-Sclc in U.S.

THOMSON REUTERS

Merck & Co - Withdrawal Based on FDA Discussions; Phase 2 Data Do not Satisfy Approval Requirements

THOMSON REUTERS

Merck & Co - Patient Enrollment Continues in Ideate-Lung02 Phase 3 Trial for Ifinatamab Deruxtecan

THOMSON REUTERS

Merck & Co - Two Additional Phase 3 Trials Underway for Ifinatamab Deruxtecan in Crpc and Escc

THOMSON REUTERS

Nordhealth Insider Boosts Stake in Cloud Healthcare SaaS Provider

UnitedHealth Announces R$ 0.115248942 Dividend Per Unit for 3Q 2026

Exchange-Traded Funds Rise US Equities Advance After Midday

MT Newswires Live

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PLC closed 31.92% below its 52-week high of $22.65, which the company reached on October 3rd.The stock outperformed some of its competitors Friday, as Johnson & Johnson  rose 0.20% to $271.22, Procter & Gamble Co.  rose 0.38% to $146.23, and Abbott Laboratories  rose 0.22% to $101.29.Trading volume  eclipsed its 50-day average volume of 2.8 M.Data source: Dow Jones Market Data, FactSet. 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Olumiant was previously approved for adults with moderately to severely active rheumatoid arthritis and severe alopecia areata.\"The visible and often extensive hair loss that comes with severe alopecia areata can have a profound impact on anyone, especially adolescents who are at a pivotal stage of life,\" Lilly Immunology president Adrienne Brown said. \"Expanding Olumiant to patients as young as 12 provides them a much-needed treatment choice and reinforces our commitment to advancing care for people living with immune-mediated 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