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JPMORGAN HEALTHCARE LEADERS ETF

59.56

+0.08390.14%

Post-market: 59.47-0.0839-0.14%16:10 EDT

Volume:46

Turnover:3K

Market Cap:8.93M

PE:- -

High:59.56

Open:59.47

Low:59.56

Close:59.47

52wk High:64.69

52wk Low:53.59

Shares:150.00K

Float Shares:150.00K

Volume Ratio:0.55

T/O Rate:0.03%

Dividend:0.51

Dividend Rate:0.86%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

Merck in License Pact Worth up to $2.13 Billion with SciBrunch Therapeutics

Lilly Launches Initiative to Expand Diabetes, Obesity Drug Access

MT Newswires Live

Eli Lilly launches ‘Lilly Change the Course Commitment’

Merck enters global license agreement with SciBrunch Therapeutics for SPR2015

Merck Enters into Exclusive Global License Agreement with Scibrunch Therapeutics for Spr2015, an Investigational Oral Kras G12d (On) Inhibitor

Eli Lilly - to Register Diabetes and Obesity Medicines in Lmics and Expand Access

THOMSON REUTERS

Eli Lilly - Aims to Treat Equal Number of Patients in Lmics and High-Income Countries by 2040

THOMSON REUTERS

Merck & Co - to Record $400 Mln Pre-Tax Charge, $0.13 Per Share, in Q3 2026

THOMSON REUTERS

Merck & Co - Deal Includes $400 Mln Upfront, Total Potential Value $2.13 Bln; Deal Closed

THOMSON REUTERS

Merck & Co Inc: Under Agreement, Scibrunch Granted Co Exclusive Rights to Develop, Manufacture & Commercialize Spr2015 Worldwide

THOMSON REUTERS

JPMorgan Adjusts Price Target on Eli Lilly to $1,500 From $1,400, Maintains Overweight Rating

MT Newswires Live

Merck's Keytruda Subcutaneous Formulation Approved for Launch in China

Ingenia Therapeutics Expects USD 5 Million MK-8748 Milestone Payment from Merck Unit Eyebiotech

Eli Lilly's Olumiant Gets FDA Approval for Severe Alopecia Areata in Adolescents

MT Newswires Live

Nektar selloff on trial brings ‘strong entry point,’ says BTIG

Huadong Medicine's Innovative Oral Small Molecule GLP-1 Agonist HDM1002 Achieves Positive Phase III Weight Loss Results

Analysts Have Conflicting Sentiments on These Healthcare Companies: Roivant Sciences (ROIV) and Johnson & Johnson (JNJ)

US FDA Approves AbbVie's Drug for Parkinson's Disease

US FDA - Approves Juvmo (Tavapadon) for Parkinson’s Disease in Adults on Sept 25, 2026

THOMSON REUTERS

Ifinatamab Deruxtecan Biologics License Application for Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily Withdrawn

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