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Vanguard Health Care ETF

319.96

-1.0000-0.31%

Pre-market: 319.960.00000.00%04:00 EDT

Volume:205.70K

Turnover:65.69M

Market Cap:19.25B

PE:34.74

High:320.67

Open:319.30

Low:317.21

Close:320.96

52wk High:330.75

52wk Low:249.57

Shares:60.18M

Float Shares:60.18M

Volume Ratio:0.97

T/O Rate:0.34%

Dividend:4.74

Dividend Rate:1.48%

EPS(TTM):9.21

EPS(LYR):41.51

ROE:3.75%

ROA:0.89%

PB:0.97

PE(LYR):7.71

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Overview Company News Filings

China's Shandong Xinhua Profit Drops on Domestic, International Competition

China's Innovent Biologics H1 Revenue, Profit Rise on Strong Product Sales

Austar Lifesciences H1 Profit Drops on Higher R&D Spending

WuXi Biologics H1 Net Profit up on Margin Expansion

Stick with Value Stocks Until Everyone Starts Talking About Them - and as of Now They're Still Under the Radar, This Wall Street Firm Says

Merck & Company (MRK) Gets a Buy from Scotiabank

Merck price target raised to $170 from $145 at Argus

Parabilis Medicines Appoints Former J&J Oncology Executive Craig Tendler to Board

Merck price target raised to $180 from $155 at Wolfe Research

Analysts Offer Insights on Healthcare Companies: Boston Scientific (BSX) and Eli Lilly & Co (LLY)

Molecular Partners H1 Net Loss Narrows on Lower R&D Expenses

Merck (MRK) Stock May Be 35% Undervalued After Cancer Vaccine Data

Simply Wall St.

US FDA Expands Approval for J&J's Drug for Rare Blood Disorder

FDA Approves J&J Imaavy for Warm Autoimmune Hemolytic Anemia Treatment

FDA Approves Imaavy® as First-Ever Treatment for Warm Autoimmune Hemolytic Anemia (Waiha), Representing a Landmark Advancement for Patients

THOMSON REUTERS

Oruka Therapeutics Names Todd Edwards Chief Commercial Officer

Eli Lilly Stock (LLY) in Focus as Hedge Fund Titan Ken Griffin Quadruples Position

Sector Update: Healthcare

MT Newswires Live

Exchange-Traded Funds Fall, US Equities Mixed After Midday

MT Newswires Live

Eli Lilly’s New Obesity Drug LY3549492 Moves Forward With Completed Phase 1 Trial

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FDA Expands Approval for J&J's Drug for Rare Blood Disorder","url":"https://stock-news.laohu8.com/highlight/detail?id=2662320194","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2662320194?lang=en_us&edition=fundamental","pubTime":"2026-08-25 06:32","pubTimestamp":1787610721,"startTime":"0","endTime":"0","summary":"US FDA expands approval for J&J's drug for rare blood disorderAug 24 (Reuters)-The U.S. Food and Drug Administration has approved the expanded use of Johnson & Johnson'sJNJ.Ndrug to treat a rare blood disorder, the company said on 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Approves J&J Imaavy for Warm Autoimmune Hemolytic Anemia Treatment","url":"https://stock-news.laohu8.com/highlight/detail?id=2662913201","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2662913201?lang=en_us&edition=fundamental","pubTime":"2026-08-25 06:31","pubTimestamp":1787610683,"startTime":"0","endTime":"0","summary":"FDA approves J&J IMAAVY for warm autoimmune hemolytic anemia treatmentFDA cleared IMAAVY  for warm autoimmune hemolytic anemia in patients aged 12+ who are current or prior corticosteroid users.Decision makes IMAAVY the first treatment specifically proven safe and effective for wAIHA, based on the Phase 2/3 ENERGY trial.Trial data showed a mean hemoglobin increase of 1 g/dL at Week 1, with improved FACIT-Fatigue scores at Week 24.Disclaimer:This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Johnson & Johnson published the original content used to generate this news brief on August 24, 2026, and is solely responsible for the information contained 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