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ProShares Ultra Health Care

60.86

+0.59090.98%

Volume:8K

Turnover:511.56K

Market Cap:93.11M

PE:- -

High:62.20

Open:61.32

Low:60.66

Close:60.26

52wk High:64.60

52wk Low:39.32

Shares:1.53M

Float Shares:1.53M

Volume Ratio:0.25

T/O Rate:0.55%

Dividend:0.71

Dividend Rate:1.16%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

Moderna Inc Stock (MRNA) Moved Up by 10.02% on Aug 25: Drivers Behind the Movement

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

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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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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