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Agios Pharmaceuticals

31.87

-0.0500-0.16%

Volume:292.45K

Turnover:9.32M

Market Cap:1.90B

PE:-4.55

High:32.15

Open:31.85

Low:31.53

Close:31.92

52wk High:46.00

52wk Low:22.24

Shares:59.47M

Float Shares:50.09M

Volume Ratio:0.38

T/O Rate:0.58%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-7.0075

EPS(LYR):-7.1203

ROE:-34.34%

ROA:-22.24%

PB:1.85

PE(LYR):-4.48

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Overview Company News Filings

Agios Enters Exclusive Global License Agreement With Oscotec to Develop and Commercialize Next-Generation Syk Inhibitor Cevidoplenib

THOMSON REUTERS

Agios Pharmaceuticals Is Maintained at Buy by B of A Securities

Analysts Offer Insights on Healthcare Companies: Becton Dickinson (BDX), Agios Pharma (AGIO) and Healthequity (HQY)

Agios Pharmaceuticals price target lowered to $40 from $41 at BofA

BUZZ-U.S. STOCKS ON THE MOVE-Tempus AI, SOLV Energy, Replimune

BRIEF-Agios Provides Update On Phase 2B Trial Of Tebapivat In Lower-Risk Myelodysplastic Syndromes

BUZZ-U.S. STOCKS ON THE MOVE-Costco, Firefly Aerospace, Agios

Agios Pharma Won't Advance Tebapivat for Lower-Risk Myelodysplastic Syndromes

Agios Halts Development of Tebapivat in Lower-Risk MDS After Mid-Stage Trial Miss; Shares Drop Premarket

MT Newswires Live

Agios will not advance tebapivat in lower-risk myelodysplastic syndromes

Agios Pharmaceuticals Shares Fall 19% Premarket After Co to Stop Development of Its Blood Disorder Drug

THOMSON REUTERS

Agios scraps blood disorder drug program after study miss

Agios Pharmaceuticals - Tebapivat Phase 2 Trial in Sickle Cell Disease Topline Data Expected Second Half 2026

THOMSON REUTERS

Agios Pharmaceuticals - Phase 2B Trial Results for Tebapivat in Lr-Mds Did Not Meet Predefined Threshold

THOMSON REUTERS

Agios Pharmaceuticals - Tebapivat Well Tolerated With No New Safety Signals Identified

THOMSON REUTERS

Agios Pharmaceuticals - Will Not Advance Tebapivat in Lower-Risk Myelodysplastic Syndromes

THOMSON REUTERS

Analysts Offer Insights on Healthcare Companies: Clinuvel Pharmaceuticals (OtherCLVLF) and Agios Pharma (AGIO)

Will EU Thalassemia Approval for PYRUKYND Redefine Agios Pharmaceuticals' (AGIO) Mitapivat-Centric Investment Narrative?

Simply Wall St.

Analysts Are Bullish on These Healthcare Stocks: Bicara Therapeutics Inc. (BCAX), Agios Pharma (AGIO)

BRIEF-Avanzanite Bioscience’S Partner Agios Announces Pyrukynd® (Mitapivat) Approval In EU

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Pharmaceuticals price target lowered to $40 from $41 at BofA","url":"https://stock-news.laohu8.com/highlight/detail?id=2639676217","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639676217?lang=en_us&edition=fundamental","pubTime":"2026-05-29 23:28","pubTimestamp":1780068523,"startTime":"0","endTime":"0","summary":"BofA lowered the firm’s price target on Agios Pharmaceuticals (AGIO) to $40 from $41 and keeps a Buy rating on the shares after the company 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Provides Update On Phase 2B Trial Of Tebapivat In Lower-Risk Myelodysplastic Syndromes","url":"https://stock-news.laohu8.com/highlight/detail?id=2639762712","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639762712?lang=en_us&edition=fundamental","pubTime":"2026-05-29 20:32","pubTimestamp":1780057976,"startTime":"0","endTime":"0","summary":"BRIEF-Agios Provides Update On Phase 2B Trial Of Tebapivat In Lower-Risk Myelodysplastic SyndromesMay 29 (Reuters) - Agios Pharmaceuticals Inc AGIO.O:AGIOS PROVIDES UPDATE ON PHASE 2B TRIAL OF 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Pharma Won't Advance Tebapivat for Lower-Risk Myelodysplastic Syndromes","url":"https://stock-news.laohu8.com/highlight/detail?id=2639242486","media":"Dow Jones","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639242486?lang=en_us&edition=fundamental","pubTime":"2026-05-29 19:30","pubTimestamp":1780054200,"startTime":"0","endTime":"0","summary":"Agios Pharmaceuticals said it won't advance its tebapivat, an oral pyruvate kinase activator, in lower-risk myelodysplastic syndromes, after a Phase 2b trial didn't meet the company's predefined threshold to support further development in this indication.The commercial-stage biopharmaceutical company said the 24-week dose-finding trial evaluated once-daily tebapivat in 65 patients with LR-MDS and anemia.The primary endpoint was transfusion independence, defined as eight consecutive weeks without a transfusion during the 24-week treatment period. Agios said tebapivat demonstrated evidence of biological activity, but that it didn't see clinical benefit in a sufficient proportion of patients or subgroup of patients to meet the company's predefined threshold for advancement.Tebapivat was well tolerated across all dose levels, with no new safety signals identified.Agios said tebapivat is also being evaluated in a Phase 2 trial for the treatment of sickle cell disease, with top-line data ant","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":"-1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["AGIO","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2639162624","title":"Agios Halts Development of Tebapivat in Lower-Risk MDS After Mid-Stage Trial Miss; Shares Drop Premarket","url":"https://stock-news.laohu8.com/highlight/detail?id=2639162624","media":"MT Newswires Live","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2639162624?lang=en_us&edition=fundamental","pubTime":"2026-05-29 19:27","pubTimestamp":1780054063,"startTime":"0","endTime":"0","summary":"Agios Pharmaceuticals  is set to discontinue development of tebapivat for lower-risk myelodysplastic syndromes after a phase 2b study failed to meet the company's threshold for further advancement, the company said on Friday.The open-label trial evaluated three dose levels of the oral pyruvate kinase activator in 65 patients with lower-risk MDS and anemia, it said. The primary endpoint measured transfusion independence over eight consecutive weeks during a 24-week treatment period, it added.Agios said tebapivat showed biological activity and was well tolerated, with no new safety concerns identified. However, the company said clinical benefit was not observed in enough patients to justify continued development in the indication, it added.Shares of Agios more down more than 6% in recent premarket trading.","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":"-2","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4139","SSI","AGIO"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2639624969","title":"Agios will not advance tebapivat in lower-risk myelodysplastic 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