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Xtrackers Nifty 500 India ETF

22.51

+0.04500.20%

Volume:900

Turnover:20.26K

Market Cap:4.50M

PE:- -

High:22.51

Open:22.51

Low:22.51

Close:22.47

52wk High:27.40

52wk Low:20.52

Shares:200.00K

Float Shares:200.00K

Volume Ratio:6.28

T/O Rate:0.45%

Dividend:0.08

Dividend Rate:0.35%

ROE:--

ROA:--

PB:--

PE(LYR):- -

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Overview Company News Filings

Relmada Q2 2026 earnings: R&D spending rises ahead of planned IND filings

CARSGEN-B Receives IND Clearance from Chinese Drug Regulator for Novel Cell Therapy Targeting Lymphoma

Surrozen Reports Second Quarter 2026 Financial Results and Provides Business Update

Oculis Reports Q2 2026 Financial Results and Provides Company Update

Press Release: Relmada Therapeutics Reports Second Quarter 2026 Financial Results and Provides Business Update

Press Release: Prime Medicine Reports Second Quarter 2026 Financial Results and Provides Business Updates

Press Release: Whitehawk Therapeutics Reports Second Quarter 2026 Financial Results and Recent Highlights

Press Release: Avalo Therapeutics Reports Second Quarter 2026 Financial Results and Recent Business Updates

Press Release: Amylyx Pharmaceuticals Reports Second Quarter 2026 Financial Results

Press Release: Zai Lab Announces Second Quarter 2026 Financial Results and Recent Corporate Updates

Charles River Says Biotech Demand Is Back — Bookings Hit Four-Year High

Benzinga Earnings

BriaCell Receives FDA Clearance to Initiate Bria-PROS+™ Clinical Study in Prostate Cancer

India's Central Bank Holds Key Rate Steady for Fifth Consecutive Meeting, Cites 'Moderate' Core Inflation

Ultragenyx Reports Second Quarter 2026 Financial Results and Corporate Update

OnKure Therapeutics Reports Second Quarter 2026 Financial Results and Provides Business Highlights

Syndax Reports Second Quarter 2026 Financial Results and Provides Business Update

Beam Therapeutics Reports Second Quarter 2026 Financial Results and Announces First Patient Dosed in Global Pivotal Cohort of BEAM-302 Trial in Alpha-1 Antitrypsin Deficiency (AATD)

HAIXI PHARMA Advances Oral nAMD Treatment with FDA Trial Approval and New Chinese Study

CARsgen Therapeutics Receives China IND Clearance for Multiple Myeloma Therapy; Shares Up 3%

MT Newswires Live

Caliway Biopharma Submits China Phase 1 IND for CBL-514 Fat-Reduction Drug

MT Newswires Live

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Initiation of the. Phase 3 RESCUE registrational program upon IND clearance.-- Sepranolone IND filing expected by year-end 2026 and initiation of Phase. 2 proof-of-concept study in Prader-Willi Syndrome upon IND clearance.-- Strengthened the leadership team with appointment of Bipin Dalmia as. -- Added to the Russell 2000 and Russell 3000 Indexes effective June. -- Cash balance of $217.7 million as of June 30, 2026, expected to fund. operations through 2029, including completion of the NDV-01 Phase 3","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IND","LU0347712357.USD","LU2413666426.HKD","LU1543694498.USD","IE00B1BXHZ80.USD","LU1721429741.USD","LU2237443622.USD","BK4232","ALLO","LU2746668974.SGD","RLMD","BK4006","IE00BKVL7J92.USD","CMC","BK4567","LU2092937221.SGD","LU0149725797.USD","BK4588","BK4585","LU0882574139.USD","IE00BN0W2T93.GBP","LU0971096721.USD","LU2041044095.USD","BK4139","LU2089279066.USD","BK4007","LU2237443895.HKD","IE00BN0W2W23.USD","LENZ","IE00BZ1G4Q59.USD","IE00BHPRN162.USD","LU2237443549.SGD","EES","R","LU0170899867.USD","LU2237443465.HKD","LU2237443978.SGD","LU1721428933.USD","IE00BFXG1179.USD","IE00BN0W2V16.EUR","BK4539","LU1721429402.USD","BK4505","A","PWS","LU2413666699.HKD","LU2746668461.USD","LU2229751404.USD","BK4121","PSIL"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2657963672","title":"Press Release: Prime Medicine Reports Second Quarter 2026 Financial Results and Provides Business Updates","url":"https://stock-news.laohu8.com/highlight/detail?id=2657963672","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2657963672?lang=en_us&edition=fundamental","pubTime":"2026-08-06 20:01","pubTimestamp":1786017660,"startTime":"0","endTime":"0","summary":"-- IND and CTA clearances in the United States and New Zealand establish a global Phase 1/2 program for PM577a in Wilson disease; study startup activities underway, with initial clinical data in 2027 ","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["VEGI","CF","DBMF","CTA","SDMF","BK4093","BK4139","BK4585","LU0630314457.HKD","BK4588","IND","ISMF","TFPN","LABU","BK4195","WD","BK4229","LU0345780950.USD","JPFP","PRME","LU0345781412.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2657636277","title":"Press Release: Whitehawk Therapeutics Reports Second Quarter 2026 Financial Results and Recent Highlights","url":"https://stock-news.laohu8.com/highlight/detail?id=2657636277","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2657636277?lang=en_us&edition=fundamental","pubTime":"2026-08-06 20:00","pubTimestamp":1786017600,"startTime":"0","endTime":"0","summary":"financing. The financing included participation from existing investors. including Avoro Capital, QVT, Coastlands Capital, KVP Capital, ADAR1. Capital Management, Acuta Capital Partners, StemPoint Capital LP, Invus,as well as members of Whitehawk's executive team.-- Continued to enroll patients into ongoing Phase 1 trials for HWK-007 and. -- HWK--007 is being evaluated in patients with non-squamous, EGFR. cancer; and endometrial cancer . The study design was. presented as a Trials-in-Progress poster at the American Society. -- Entered into a new option agreement with Hangzhou DAC for access to. CPT113 for use in up to five additional ADC programs. Whitehawk's ADC. platform leverages CPT113 as the core linker-payload technology, adding. bioconjugation process to support improved stability and therapeutic","market":"fut","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4080","BK4231","BK4232","LENZ","IND","NETL","BK4139","ADC","R","BK4007","BK4539","BK4022","WHWK"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2657680722","title":"Press Release: Avalo Therapeutics Reports Second Quarter 2026 Financial Results and Recent Business Updates","url":"https://stock-news.laohu8.com/highlight/detail?id=2657680722","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2657680722?lang=en_us&edition=fundamental","pubTime":"2026-08-06 19:00","pubTimestamp":1786014000,"startTime":"0","endTime":"0","summary":"-- Plans to initiate a registrational Phase 3 program evaluating abdakibart. in hidradenitis suppurativa  in the first half of 2027. -- Expanded pipeline with AVTX-010, a long-acting next-generation. anti-IL-1<BETA> antibody, with IND submission planned for the first half. -- Cash, cash equivalents and investments of $472.2 million as of June 30,abdakibart in HS in the first half of 2027.HS as well as other inflammatory disorders. The Company expects to submit. an Investigational New Drug  application in the first half of 2027.-- Appointed Ron Philip to its Board of Directors. Ron contributes deep. strategic and commercial expertise, with a proven track record of. -- Added to the Russell 2000 and Russell 3000 Indexes as part of the. 2026. Net cash used in operating activities was $37.7 million for the six. months ended June 30, 2026. Avalo's current cash, cash equivalents, and. investments are expected to fund operations into 2029.-- Research and development expenses were $23.4 million","market":"us","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4007","BK4139","AVTX","BK4232","BK4022","LENZ","IND","BK4539","R"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2657638343","title":"Press Release: Amylyx Pharmaceuticals Reports Second Quarter 2026 Financial Results","url":"https://stock-news.laohu8.com/highlight/detail?id=2657638343","media":"Dow Jones","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2657638343?lang=en_us&edition=fundamental","pubTime":"2026-08-06 19:00","pubTimestamp":1786014000,"startTime":"0","endTime":"0","summary":"--  Last participant completed final study visit in the 16-week. double-blind period of the pivotal Phase 3 LUCIDITY trial of avexitide in. post-bariatric hypoglycemia; topline data on track and anticipated in. CAMBRIDGE, Mass.----August 06, 2026--Amylyx Pharmaceuticals, Inc.   today reported financial and business results for the second quarter ended June 30, 2026.\"With the last participant's final study visit recently completed, we are eagerly anticipating the expected topline data readout of the pivotal Phase 3 LUCIDITY trial in post-bariatric hypoglycemia in late August or early September,\" said Joshua Cohen and Justin Klee, Co-CEOs of Amylyx. \"In parallel, we are continuing to advance our NDA readiness and our pre-commercial work to support a potential submission and commercial launch of avexitide in 2027, if approved. At ENDO in June 2026, we activated our disease state education campaign, 'Uncover the Mystery of Post-Bariatric Hypoglycemia,' designed to increase awareness and un","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4007","AMLX","IND","PBH","ASO","BK4561","BK4200"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2657687386","title":"Press Release: Zai Lab Announces Second Quarter 2026 Financial Results and Recent Corporate Updates","url":"https://stock-news.laohu8.com/highlight/detail?id=2657687386","media":"Dow Jones","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2657687386?lang=en_us&edition=fundamental","pubTime":"2026-08-06 18:30","pubTimestamp":1786012200,"startTime":"0","endTime":"0","summary":"--  The Company advanced multiple global oncology and immunology programs. toward key clinical and regulatory milestones, with significant pipeline. --  Global Phase 1 data for zocilurtatug pelitecan  in combination. with a PD-L1 inhibitor in first-line SCLC to be presented at ESMO 2026;planned initiation of a registrational Phase 3 study later this year. --  Registrational Phase 3 DLLEVATE study evaluating zoci in second-line. plus SCLC remains on track, with enrollment expected to be completed in. the first half of 2027, supporting a potential U.S. accelerated approval. --  Global Phase 1/1b study of ZL-1503, a potential first-in-class. long-acting IL-13/IL-31R<ALPHA> bispecific antibody for the treatment of. atopic dermatitis, continues to advance, with 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