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VanEck Pharmaceutical ETF

108.06

-0.0800-0.07%

Post-market: 108.060.00000.00%19:30 EDT

Volume:272.52K

Turnover:29.38M

Market Cap:1.01B

PE:87.56

High:108.33

Open:108.14

Low:107.29

Close:108.14

52wk High:118.00

52wk Low:90.60

Shares:9.39M

Float Shares:9.39M

Volume Ratio:0.61

T/O Rate:2.90%

Dividend:2.18

Dividend Rate:2.02%

EPS(TTM):1.23

EPS(LYR):0.7765

ROE:--

ROA:--

PB:--

PE(LYR):139.17

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Overview Company News Filings

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

ETF Weekly | QCML Soars 27%; INTW, AMUU, FBL, AMDL Jump 26%; SOXL Rallies 22%; Semiconductor Longs Lead

Novo Nordisk (0QIU) Receives a Hold from Bank of America Securities

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Biologics License Application for Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily Withdrawn

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

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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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