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HARBOR HEALTH CARE ETF

32.72

+0.28570.88%

Post-market: 32.720.00000.00%16:10 EDT

Volume:2K

Turnover:74.53K

Market Cap:41.71M

PE:- -

High:32.81

Open:32.81

Low:32.72

Close:32.43

52wk High:35.61

52wk Low:27.50

Shares:1.28M

Float Shares:1.28M

Volume Ratio:0.61

T/O Rate:0.18%

Dividend:0.08

Dividend Rate:0.23%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

Analysts’ Opinions Are Mixed on These Healthcare Stocks: Ascendis Pharma (ASND), Lakefront Biotherapeutics (LKFT) and 10x Genomics (TXG)

Eli Lilly price target raised to $1,500 from $1,400 at JPMorgan

Xilio Therapeutics Names Yariv Houvras Chief Medical Officer

Lilly Launches Initiative to Expand Diabetes, Obesity Drug Access

MT Newswires Live

Eli Lilly launches ‘Lilly Change the Course Commitment’

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

Zymeworks sees FY26 revenue $278M-$292M, consensus $304.04M

Ascendis Pharma Price Target Maintained with a $300.00/Share by Cantor Fitzgerald

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

MT Newswires Live

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

MT Newswires Live

EBR Systems advances FDA approval process for new WiSE manufacturing site

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

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

Top Midday Stories: Akamai's $11.6 Billion Anthropic Deal; Scholastic Q1 Loss Widens; Nektar Awarded $90 Million in Eli Lilly Case

MT Newswires Live

Sector Update: Healthcare Stocks Edge Higher Premarket Friday

MT Newswires Live

Novo Bets on Next Chapter While Eli Lilly Extends Its GLP-1 Dominance

Legend Biotech Says Five-Year Carvykti Data Show 50% of Patients Remained Progression-Free and Alive

MT Newswires Live

Legend Biotech Reports Five-Year CARVYKTI Survival Data in Earlier-Line Myeloma

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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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Shs Chess Depository Interests Repr 1 Sh ( ($AU:EBR) ). EBR Systems, developer of the WiSE wi...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/ebr-systems-advances-fda-approval-process-for-new-wise-manufacturing-site?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/company-announcements/ebr-systems-advances-fda-approval-process-for-new-wise-manufacturing-site?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["PSCH","GDOC","GNMX","MEDI","BK4585","BMED","EES","IBB","IYH","TECB","RSPH","MRNY","TBXU","SYNB","MRNX","XLVX","FRTY","BBP","IDNA","LFSC","LABU","BK4588","NVIB","PINK","IEIH"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2670404993","title":"Nektar 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Lilly Gets Expanded Label Approval from FDA for Alopecia Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2670442248","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670442248?lang=en_us&edition=fundamental","pubTime":"2026-09-26 05:26","pubTimestamp":1790371560,"startTime":"0","endTime":"0","summary":"Eli Lilly received expanded label approval from the Food and Drug Administration for Olumiant, a drug for pediatric patients 12 years of age or older with severe alopecia areata.The company said Friday that the FDA had approved the expanded U.S. label for the drug, known generically as baricitinib, based on the results of a Phase 3 study. 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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