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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

Novo Nordisk Says New Obesity Drug Outperformed Lilly's Zepbound in Phase 3 Trial

J&J says Caplyta Phase 3 study in bipolar I met primary endpoint

Novo Stock (NVO) Sinks Despite Beating Eli Lilly in New CagriSema Obesity Trial

AbbVie, Iambic Sign Multiyear Drug Discovery Deal

MT Newswires Live

AbbVie Partners with Iambic to Accelerate AI-Driven Small-Molecule Drug Discovery

Johnson & Johnson Says Phase 3 Trial Shows Caplyta Cuts Bipolar I Mania Symptoms by Week 3

Abbvie and Iambic Announce Collaboration to Accelerate AI-Driven Drug Discovery

THOMSON REUTERS

Abbvie - Iambic to Receive Upfront Payment, Milestone Payments, and Tiered Royalties from Collaboration

THOMSON REUTERS

Abbvie - Partnership to Accelerate Small Molecule Drug Discovery in Immunology, Neuroscience, Oncology

THOMSON REUTERS

J&J - Caplyta Demonstrates Statistically Significant Rapid Reduction in Manic Symptoms at Week 3

THOMSON REUTERS

Caplyta® (Lumateperone) Shows Significant and Rapid Improvement in Bipolar Mania in Pivotal Phase 3 Study

THOMSON REUTERS

J&J - Caplyta Well-Tolerated; Dry Mouth and Nausea Most Common Adverse Events

THOMSON REUTERS

Adarx Pharmaceuticals: IPO Price Expected Between $15 and $17 Per Share

Oura Files for Initial Public Offering on Nasdaq

MT Newswires Live

LIVE Markets-Big Beauty Faces Growing Threat from AI, Smaller Rivals

ADARx Pharmaceuticals to Sell 21.9 Million Shares at $15-$17 Each in IPO

Smart Ring Maker Oura Eyes $15.6 Billion IPO Valuation in Fall Listings Demand Test

Oura - Eli Lilly Interested in Purchasing up to $100 Mln; Dragoneer up to $300 Mln in IPO - SEC Filing

THOMSON REUTERS

Japan Health Ministry Approves Merck’s Keytruda QLEX for Subcutaneous Use Across Keytruda Indications

Merck’s Keytruda Qlex™ (Pembrolizumab and Berahyaluronidase Alfa-Pmph) Approved in Japan for Subcutaneous Administration for All Keytruda® (Pembrolizumab) Indications Approved in Japan

THOMSON REUTERS

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