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Fidelity MSCI Health Care Index ETF

80.60

+0.02000.02%

Post-market: 80.600.00000.00%19:30 EDT

Volume:210.62K

Turnover:16.95M

Market Cap:3.49B

PE:- -

High:80.81

Open:80.81

Low:80.23

Close:80.58

52wk High:85.46

52wk Low:67.77

Shares:43.35M

Float Shares:43.35M

Volume Ratio:0.47

T/O Rate:0.49%

Dividend:1.02

Dividend Rate:1.27%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

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

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Biologics License Application for Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily Withdrawn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

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Keytruda Subcutaneous Formulation Approved for Launch in China","url":"https://stock-news.laohu8.com/highlight/detail?id=1195604847","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1195604847?lang=en_us&edition=fundamental","pubTime":"2026-09-28 16:38","pubTimestamp":1790584732,"startTime":"0","endTime":"0","summary":"The National Medical Products Administration (NMPA) official website indicated on September 28 that Merck's pembrolizumab injection (subcutaneous injection, namely MK-3475A) has been approved 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Therapeutics Expects USD 5 Million MK-8748 Milestone Payment from Merck Unit Eyebiotech","url":"https://stock-news.laohu8.com/highlight/detail?id=2670280899","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670280899?lang=en_us&edition=fundamental","pubTime":"2026-09-28 16:32","pubTimestamp":1790584375,"startTime":"0","endTime":"0","summary":"Ingenia Therapeutics expects USD 5 million MK-8748 milestone payment from Merck unit EyebiotechIngenia Therapeutics expects to receive a milestone payment tied to MK-8748, licensed to Merck unit 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Lilly's Olumiant Gets FDA Approval for Severe Alopecia Areata in Adolescents","url":"https://stock-news.laohu8.com/highlight/detail?id=2670287686","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670287686?lang=en_us&edition=fundamental","pubTime":"2026-09-28 16:09","pubTimestamp":1790582940,"startTime":"0","endTime":"0","summary":"Eli Lilly  said Friday the US Food and Drug Administration approved its drug, Olumiant, for patients ages 12 and older with severe alopecia areata, expanding its US approval to adolescents.The approval was based on 36-week data from a Phase 3 trial. The company said the approval was based on a phase 3 trial that showed 42% of patients taking 4 mg and 27% taking 2 mg achieved at least 80% scalp hair coverage, compared with 5% on placebo.The drug carries an FDA boxed warning for serious infections, cancer, major cardiovascular events, blood clots, and death, Lilly 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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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