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iShares U.S. Healthcare ETF

70.40

0.0000

Post-market: 70.400.00000.00%19:30 EDT

Volume:615.74K

Turnover:43.32M

Market Cap:3.91B

PE:6.34

High:70.61

Open:70.61

Low:70.09

Close:70.40

52wk High:74.59

52wk Low:59.47

Shares:55.60M

Float Shares:55.60M

Volume Ratio:1.19

T/O Rate:1.11%

Dividend:0.81

Dividend Rate:1.15%

EPS(TTM):11.10

EPS(LYR):3.06

ROE:6.01%

ROA:0.87%

PB:1.40

PE(LYR):23.01

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Overview Company News Filings

Merck Has Two Overlooked Pipeline Catalysts Coming Before Year-End, UBS Says

MT Newswires Live

Oruka Therapeutics' Psoriasis Treatment Maintains 'Competitive Profile' After Positive Clinical Data, UBS Says

MT Newswires Live

S&P 500 Top and Bottom Performing Stocks at About 12:00 P.m. EDT

Eli Lilly and Co Stock (LLY) Moved Up by 3.73% on Sep 24: A Full Analysis

Lilly's Next-Gen Obesity Efforts Could Tip Scales Further in Its Favor, Citi Says

Alert on EOG CFO Appointment Incorrectly Tagged to J&J Withdrawn

EOG Resources Announces Ann Janssen's Retirement and Jeff Hibbard as Next CFO

THOMSON REUTERS

UnitedHealth Adds Jodee Kozlak as Chief Administrative Officer Effective Sept. 28, 2026

UnitedHealth Group Announces Addition to Leadership Team

THOMSON REUTERS

UnitedHealth - Appoints Jodee Kozlak as Chief Administrative Officer Effective Sept. 28, 2026

THOMSON REUTERS

Merck's Drug for Diabetes-Related Eye Disease Meets Trial Goal

Health Canada Approves AbbVie’s Epkinly Combo for Relapsed or Refractory Follicular Lymphoma in Adults

Epkinly® Receives Health Canada Approval for Adults with Follicular Lymphoma

THOMSON REUTERS

Eli Lilly Gets FDA OK for Onswik Once-Weekly Insulin Injection

Merck Says Remigromig Meets Primary Endpoint in Pivotal Brunello Trial for Diabetic Macular Edema

Eli Lilly - Onswik Kwikpen to be Available in U.S. in 500 Units/Ml and 1,000 Units/Ml Concentrations

THOMSON REUTERS

U.S. Food and Drug Administration (FDA) Approves Lilly's Onswik™ (Insulin Efsitora Alfa-Gobe), a Once-Weekly Basal Insulin Injection Treatment for Adults Living with Type 2 Diabetes

THOMSON REUTERS

Merck & Co - Higher Rates of Pdr, Vitreous Hemorrhage, and Discontinuations with Remigromig

THOMSON REUTERS

Merck’s Remigromig, a Tri-Specific Agonist of the Wingless-Related Integration Site (Wnt) Pathway, Met Primary Endpoint in the Pivotal Phase 2B/3 Brunello Study of Adults with Diabetic Macular Edema

THOMSON REUTERS

Merck & Co Inc: Both Doses of Remigromig were Generally Well Tolerated

THOMSON REUTERS

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This compares favorably with rival product, AbbVie's  Skyrizi, which rose to 53% from 43% in the same period, UBS analysts said.The safety data was also consistent with prior data, as treatment-emergent adverse events were 36% in the period of week 16 to 28, compared with 51% during week zero to 16. 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Next-Gen Obesity Efforts Could Tip Scales Further in Its Favor, Citi Says","url":"https://stock-news.laohu8.com/highlight/detail?id=2669149540","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2669149540?lang=en_us&edition=fundamental","pubTime":"2026-09-24 21:46","pubTimestamp":1790257597,"startTime":"0","endTime":"0","summary":"BUZZ-Lilly's next-gen obesity efforts could tip scales further in its favor, Citi says** Eli LillyLLY.Nis expected to present mid-stage data next week on eloralintide, its next-generation obesity drug candidate, in combination with its blockbuster weight-loss drug Zepbound, chemically known as tirzepatide** Citi analysts say the data will be a test of whether eloralintide can extend tirzepatide's efficacy without compromising tolerability or persistence** Eloralintide belongs to the class of drugs that mimic the pancreatic hormone amylin with the potential of less severe side effects than the popular GLP-1 class of 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