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Tema Heart & Health ETF

36.22

+0.51001.43%

Post-market: 36.220.00000.00%19:30 EDT

Volume:683

Turnover:24.64K

Market Cap:53.60M

PE:- -

High:36.22

Open:35.75

Low:35.75

Close:35.71

52wk High:38.87

52wk Low:31.87

Shares:1.48M

Float Shares:1.48M

Volume Ratio:0.23

T/O Rate:0.05%

Dividend:0.47

Dividend Rate:1.31%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

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

Thermo Fisher Scientific: Thermo Fisher Scientific Will Offer Evosep Eno Separation Platform as Part of Portfolio of Mass Spectrometry Solutions

THOMSON REUTERS

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

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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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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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