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JPMORGAN HEALTHCARE LEADERS ETF

60.50

0.0000

Volume:11

Turnover:662.21

Market Cap:9.08M

PE:- -

High:60.50

Open:60.50

Low:60.50

Close:60.50

52wk High:64.69

52wk Low:50.40

Shares:150.00K

Float Shares:150.00K

Volume Ratio:0.14

T/O Rate:0.01%

Dividend:0.51

Dividend Rate:0.85%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

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Biologics License Application for Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily Withdrawn

Perrigo Co. PLC Stock Outperforms Competitors on Strong Trading Day

Eli Lilly Gets Expanded Label Approval from FDA for Alopecia Drug

FDA Approves Lilly's Olumiant (Baricitinib) for Pediatric Patients 12 Years of Age and Older with Severe Alopecia Areata

THOMSON REUTERS

Merck, Daiichi Sankyo Withdraw US Application for Lung Cancer Drug

Merck, Daiichi Sankyo voluntarily withdraw BLA for ifinatamab deruxtecan

Merck & Co - Daiichi Sankyo and Merck Withdraw Bla for Ifinatamab Deruxtecan in Es-Sclc in U.S.

THOMSON REUTERS

Merck & Co - Withdrawal Based on FDA Discussions; Phase 2 Data Do not Satisfy Approval Requirements

THOMSON REUTERS

Merck & Co - Patient Enrollment Continues in Ideate-Lung02 Phase 3 Trial for Ifinatamab Deruxtecan

THOMSON REUTERS

Merck & Co - Two Additional Phase 3 Trials Underway for Ifinatamab Deruxtecan in Crpc and Escc

THOMSON REUTERS

UnitedHealth Announces R$ 0.115248942 Dividend Per Unit for 3Q 2026

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PLC closed 31.92% below its 52-week high of $22.65, which the company reached on October 3rd.The stock outperformed some of its competitors Friday, as Johnson & Johnson  rose 0.20% to $271.22, Procter & Gamble Co.  rose 0.38% to $146.23, and Abbott Laboratories  rose 0.22% to $101.29.Trading volume  eclipsed its 50-day average volume of 2.8 M.Data source: Dow Jones Market Data, FactSet. 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Olumiant was previously approved for adults with moderately to severely active rheumatoid arthritis and severe alopecia areata.\"The visible and often extensive hair loss that comes with severe alopecia areata can have a profound impact on anyone, especially adolescents who are at a pivotal stage of life,\" Lilly Immunology president Adrienne Brown said. \"Expanding Olumiant to patients as young as 12 provides them a much-needed treatment choice and reinforces our commitment to advancing care for people living with immune-mediated 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