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iShares U.S. Healthcare ETF

72.38

+0.36000.50%

Pre-market: 72.380.00000.00%08:47 EDT

Volume:3.32M

Turnover:240.07M

Market Cap:3.89B

PE:6.52

High:73.21

Open:72.93

Low:72.14

Close:72.02

52wk High:74.59

52wk Low:56.44

Shares:53.70M

Float Shares:53.70M

Volume Ratio:9.40

T/O Rate:6.18%

Dividend:0.81

Dividend Rate:1.12%

EPS(TTM):11.10

EPS(LYR):3.06

ROE:6.01%

ROA:0.87%

PB:1.39

PE(LYR):23.66

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Overview Company News Filings

Merck Price Target Raised to $170.00/Share from $145.00 by Argus Research

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

PwC Data Shows Record 7,316 Deals in First Half, Strong Momentum Expected to Continue Into Late 2026

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

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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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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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