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Direxion Daily S&P Biotech Bull 3x Shares

261.30

-4.7000-1.77%

Post-market: 261.300.00000.00%19:58 EDT

Volume:227.38K

Turnover:60.97M

Market Cap:489.80M

PE:- -

High:278.96

Open:273.29

Low:261.30

Close:266.00

52wk High:341.93

52wk Low:74.95

Shares:1.87M

Float Shares:1.87M

Volume Ratio:0.94

T/O Rate:12.13%

Dividend:1.00

Dividend Rate:0.38%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

Analysts Offer Insights on Healthcare Companies: Revolution Medicines (RVMD) and Cooper Co (COO)

Taixing Employee Medical Insurance Retirement Benefits: Everything You Need to Know

FDA-Driven Zanza Delay Keeps Exelixis Fairly Valued, Supporting Willey’s Hold Rating

Entero Healthcare Subsidiary Pays GST Penalty Under Protest, Plans Refund Claim

Syngene Schedules Analyst Meet at Kotak Healthcare Forum 2026

Scholar Rock announces FDA approval of isembyld

Press Release: Abrdn Healthcare Opportunities Fund (THQ) and Abrdn World Healthcare Fund (THW) Announce New Managed Distribution Policies and Declare Monthly Distributions

Health Care Flat as Traders Rotate Back into Fuel-Sensitive Sectors - Health Care Roundup

Health Care Roundup: Market Talk

Sector Update: Healthcare

MT Newswires Live

Pharming wins FDA nod to extend Joenja use to younger APDS children

FDA approves Pharming’s Joenja® as first treatment for children with APDS in the U.S.

Pharming Gets FDA Approval for Joenja to Treat APDS in Children Aged 4-11

MT Newswires Live

Health Care Roundup: Market Talk

FDA approves Joenja tablets for children aged 4-11 with APDS

Worldwide Healthcare Trust Boosts Treasury Stock with Latest Share Buyback

Definium Therapeutics' Upcoming Phase 3 Data on DT120 to De-Risk Program, Back FDA Approval, RBC Says

MT Newswires Live

Shanghai INT Medical Clarifies Sellers in Healthcare Equity Acquisition

Analysts Offer Insights on Healthcare Companies: Medicus Pharma Ltd (MDCX) and Labcorp Holdings (LH)

Quantum BioPharma Ltd. (NASDAQ: QNTM) Filling Key Gap in MS Treatment, Cleared by FDA to Launch Historic Trials

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Pharming has secured U.S. FDA approval for new 40 mg and 50 mg twice-daily doses of Jo...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/pharming-wins-fda-nod-to-extend-joenja-use-to-younger-apds-children?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/pharming-wins-fda-nod-to-extend-joenja-use-to-younger-apds-children?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["RSPH","BK4585","IDNA","IEIH","LABU","MEDI","BK4588","BBP","NVIB","GDOC","TECB","FRTY","SYNB","PSCH","XLVX","IBB","GNMX","TBXU","MRNX","PINK","MRNY","LFSC","IYH","BMED"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2666576737","title":"FDA approves Pharming’s Joenja® as first treatment for children with APDS in the U.S.","url":"https://stock-news.laohu8.com/highlight/detail?id=2666576737","media":"GlobeNewswire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2666576737?lang=en_us&edition=fundamental","pubTime":"2026-09-12 02:00","pubTimestamp":1789149600,"startTime":"0","endTime":"0","summary":"FDA approval expands Joenja indication to include children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) ages 4 to 11 who weigh at least 27kgNewly approved Joenja doses are ex","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2026/09/11/3360484/0/en/fda-approves-pharming-s-joenja-as-first-treatment-for-children-with-apds-in-the-u-s.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4588","LABU","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2666765235","title":"Pharming Gets FDA Approval for Joenja to Treat APDS in Children Aged 4-11","url":"https://stock-news.laohu8.com/highlight/detail?id=2666765235","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2666765235?lang=en_us&edition=fundamental","pubTime":"2026-09-12 01:16","pubTimestamp":1789147000,"startTime":"0","endTime":"0","summary":"Pharming's  Joenja tablets have been approved to treat activated phosphoinositide 3-kinase delta syndrome, or APDS, in children 4-11 years who weigh at least 27 kg, the US Food and Drug Administration said Friday.Joenja was first approved in 2023 for the same indication in patients 12 years and older, the regulator said. APDS is a rare genetic disorder that impairs cells of the immune system.Shares were about 1.6% higher in afternoon trading.Price: 10.98, Change: +0.17, Percent Change: +1.60","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4588","BK4585","BK4139","PHAR","LABU"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2666575978","title":"Health Care Roundup: Market Talk","url":"https://stock-news.laohu8.com/highlight/detail?id=2666575978","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2666575978?lang=en_us&edition=fundamental","pubTime":"2026-09-12 00:20","pubTimestamp":1789143600,"startTime":"0","endTime":"0","summary":"The latest Market Talks covering the Health Care sector. 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Worldwide Healthcare Trust PLC has executed a share buyback, purchasing 48...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/worldwide-healthcare-trust-boosts-treasury-stock-with-latest-share-buyback-6?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/worldwide-healthcare-trust-boosts-treasury-stock-with-latest-share-buyback-6?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["BK4581","XBI","BK4588","LABU","BRKU","BRKW","XLV","BK4585","BRKL","ACTV","LU0029874061.USD","LU0128526141.USD","BK4137","BRKC","HCSG","BRKD","ACKY"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2666257316","title":"Definium Therapeutics' Upcoming Phase 3 Data on DT120 to De-Risk Program, Back FDA Approval, RBC Says","url":"https://stock-news.laohu8.com/highlight/detail?id=2666257316","media":"MT Newswires Live","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2666257316?lang=en_us&edition=fundamental","pubTime":"2026-09-11 23:33","pubTimestamp":1789140826,"startTime":"0","endTime":"0","summary":"Definium Therapeutics'  upcoming phase 3 data on DT120 in generalized anxiety disorder or GAD is likely to further de-risk the program and back potential approval, RBC Capital Markets said in a Friday note.The first phase 3 trial in GAD met its primary endpoint and a positive data readout from the second phase 3 trial should ease residual regulatory uncertainty on the therapy's approvability, the brokerage said. Data from the second phase 3 trial is due for release \"any day now,\" RBC noted.Trial results are likely to support approval from the US Food and Drug Administration given DT120's robust efficacy data, well-powered studies, and the FDA's flexibility for neuropsychiatric drugs, according to the investment firm.RBC has an outperform rating on Definium Therapeutics, with a $66 price target.Price: 38.53, Change: +0.80, Percent Change: +2.12","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["DFTX","BK4007","BK4585","LABU","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2666736525","title":"Shanghai INT Medical Clarifies Sellers in Healthcare Equity Acquisition","url":"https://stock-news.laohu8.com/highlight/detail?id=2666736525","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2666736525?lang=en_us&edition=fundamental","pubTime":"2026-09-11 23:08","pubTimestamp":1789139337,"startTime":"0","endTime":"0","summary":"Shanghai Kindly Medical Instruments Co., Ltd. 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