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PagerDuty, Inc.

16.07

-0.2700-1.65%

Post-market: 16.070.00000.00%19:49 EDT

Volume:1.44M

Turnover:23.14M

Market Cap:1.48B

PE:-39.90

High:16.49

Open:16.49

Low:15.93

Close:16.34

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Overview Company News Filings

Sonnet’s SON-1010 Demonstrates a Strong Safety Profile in Combination with Atezolizumab for Treatment of Platinum-Resistant Ovarian Cancer, Including a Partial Response at the Highest Dose

Arvinas Presents First-in-Human Data for Investigational Oral PROTAC ARV-102 Demonstrating Blood-Brain Barrier Penetration, and Central and Peripheral LRRK2 Degradation

PagerDuty (PD) and Uber (UBER), DoorDash (DASH), GameStop (GME), LiveRamp (RAMP) Stocks Trade Down, What You Need To Know

Amneal Announces Expanded Coverage for CREXONT® (Carbidopa and Levodopa) to Enhance Access for Parkinson’s Disease Patients in the U.S.

PagerDuty (PD) Gets a Buy from Truist Financial

Investigators to Present Clinical Trial Results Showing Neflamapimod Slows Clinical Progression in Dementia with Lewy Bodies in Oral Presentation at AD/PD™ 2025

Vigil Neuroscience Presents Data on its Small Molecule TREM2 Agonist VG-3927 in Two Oral Presentations at AD/PD™ 2025 International Conference

AC Immune Reports Further Positive Interim Results from Phase 2 Trial of ACI-7104.056 Active Immunotherapy in Early Parkinson’s Disease

PagerDuty Report Finds More Than Half of Companies Have Deployed AI Agents

Cerevance Presents Topline Results from Phase 2 ASCEND Trial of Solengepras as Monotherapy Treatment for Early-Stage Parkinson’s Disease at AD/PD 2025

Aquestive Therapeutics Announces Positive Topline PK Results from its Pediatric Study and Completes the NDA Submission for Anaphylm™ (epinephrine) Sublingual Film

Tovecimig (CTX-009) Meets Primary Endpoint in the Ongoing Randomized Phase 2/3 Study in Patients with Biliary Tract Cancer

Quanterix Showcases Innovation Powered by Simoa® at AD/PD with Customer Research and New Dried Blood Spot Extraction Kit

ProMIS Neurosciences Announces Full Year 2024 Financial Results and Recent Highlights

Voyager Presents Robust Preclinical Data from Tau Targeting Gene Therapy and Antibody Programs at AD/PD™ 2025

Vaxcyte Announces Positive Topline Results from VAX-24 Infant Phase 2 Dose-Finding Study

Press Release: LAVA Reports Fourth Quarter and Full Year 2024 Financial Results and Provides a Business Update

TransCode Therapeutics Announces Initial Dosing in Fourth Cohort of Phase 1 Clinical Trial with TTX-MC138

Annovis Bio, Inc. Receives Continued Listing Standard Notice From the NYSE

Sensei Biotherapeutics Reports Favorable Preliminary Dose Expansion Data for Solnerstotug in PD-(L)1 Resistant Tumors

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in","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://www.globenewswire.com/news-release/2025/04/04/3055854/0/en/Arvinas-Presents-First-in-Human-Data-for-Investigational-Oral-PROTAC-ARV-102-Demonstrating-Blood-Brain-Barrier-Penetration-and-Central-and-Peripheral-LRRK2-Degradation.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":["PD","PSP","BK4023","LU1169589451.USD","CSF","LU1169590202.USD"],"gpt_icon":0},{"id":"2524999022","title":"PagerDuty (PD) and Uber (UBER), DoorDash (DASH), GameStop (GME), LiveRamp (RAMP) Stocks Trade Down, What You Need To Know","url":"https://stock-news.laohu8.com/highlight/detail?id=2524999022","media":"StockStory","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524999022?lang=en_us&edition=fundamental","pubTime":"2025-04-04 01:06","pubTimestamp":1743699974,"startTime":"0","endTime":"0","summary":"A number of stocks fell in the after-market session after President Trump announced \"reciprocal tariffs\" on all US imports, set at a minimum rate of 10%.Markets reacted negatively to the announcement, reflecting deep concerns among investors about the broader economic implications. The tariffs were likely seen as a significant threat to global trade flows, with the potential to slow economic growth, drive up consumer prices, and spark retaliatory measures.Wedbush analyst Dan Ives captured the prevailing market anxiety, stating, \"We would characterize this slate of tariffs as 'worse than the worst case scenario' the Street was fearing.\" His comment highlighted how the scope and severity of the tariffs far exceeded Wall Street's expectations, adding a new layer of uncertainty for businesses and investors.The stock market overreacts to news, and big price drops can present good opportunities to buy high-quality stocks.Cloud Monitoring company PagerDuty  fell 17.4%. Is now the time to buy ","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://finance.yahoo.com/news/pagerduty-pd-uber-uber-doordash-170614086.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["RAMP","GB00BDT5M118.USD","SG9999014898.SGD","BK4577","LU0719512351.SGD","LU0006306889.USD","LU0106261612.USD","BK4548","LU0127658192.USD","SG9999014880.SGD","SG9999015986.USD","LU1861219969.SGD","SG9999015978.USD","LU1861214812.USD","SG9999018857.SGD","BK4076","BK4122","BK4023","LU0353189680.USD","SG9999015945.SGD","SG9999014914.USD","LU0240878834.USD","UBER","BK4022","BK4549","LU2065171311.SGD","IE0002270589.USD","BK4505","LU0106261372.USD","IE00BFMHRM44.USD","LU1169590202.USD","BK4503","LU1064131342.USD","LU0642271901.SGD","BK4535","LU2065171402.SGD","SG9999015952.SGD","SG9999018865.SGD","PD","DASH","LU0205193047.USD","BK4209","LU1814569148.SGD","BK4551","GME","LU1316542783.SGD","IE00B19Z3B42.SGD","SGXZ31699556.SGD","SG9999014906.USD","IE00BZ199S13.USD"],"gpt_icon":1},{"id":"2524598032","title":"Amneal Announces Expanded Coverage for CREXONT® (Carbidopa and Levodopa) to Enhance Access for Parkinson’s Disease Patients in the U.S.","url":"https://stock-news.laohu8.com/highlight/detail?id=2524598032","media":"Business Wire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524598032?lang=en_us&edition=fundamental","pubTime":"2025-04-03 20:00","pubTimestamp":1743681600,"startTime":"0","endTime":"0","summary":"CREXONT added to 3 large national formularies: Veterans Administration, UnitedHealthcare and CVS Health. Increases insurance coverage to over 50% of covered lives. This expanded coverage increases CREXONT’s total U.S. insurance coverage from about 30% of covered lives at the end of 2024 to over 50%. The Company had initially set a goal to surpass 50% coverage by the end of 2025, making this milestone—achieved nine months ahead of schedule—a testament to Amneal’s commitment to broadening patient access. The VA has already added the product in its national formulary, covering approximately 10% of U.S. PD patients. UnitedHealthcare will add CREXONT to its standard prescription drug lists in the second quarter of 2025. In addition, CVS Health will add CREXONT as a \"preferred\" product to its national formulary on July 1, 2025.More \"Good On\" time with less frequent dosing: A head-to-head clinical trial showed CREXONT provides more \"Good On\" time per day, and 1.55 more hours of \"Good On\" time","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://finance.yahoo.com/news/amneal-announces-expanded-coverage-crexont-120000502.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":"yahoofinance","symbols":["BK4161","AMRX","LU1169590202.USD","BK4007","LU0256863902.USD","BK4588","LU1169589451.USD","PD","BK4585","IR","LU0256863811.USD","LU1978683503.SGD","LU0417517546.SGD","LU0124384867.USD","SG9999001440.SGD","BK4023"],"gpt_icon":0},{"id":"2524461304","title":"PagerDuty (PD) Gets a Buy from Truist Financial","url":"https://stock-news.laohu8.com/highlight/detail?id=2524461304","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524461304?lang=en_us&edition=fundamental","pubTime":"2025-04-02 19:17","pubTimestamp":1743592659,"startTime":"0","endTime":"0","summary":"In a report released today, Joel Fishbein from Truist Financial reiterated a Buy rating on PagerDuty (PD – Research Report). The company’s shares c...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/pagerduty-pd-gets-a-buy-from-truist-financial-2?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/blurbs/pagerduty-pd-gets-a-buy-from-truist-financial-2?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["LU1169589451.USD","BK4023","PD","LU1169590202.USD"],"gpt_icon":0},{"id":"2524940495","title":"Investigators to Present Clinical Trial Results Showing Neflamapimod Slows Clinical Progression in Dementia with Lewy Bodies in Oral Presentation at AD/PD™ 2025","url":"https://stock-news.laohu8.com/highlight/detail?id=2524940495","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524940495?lang=en_us&edition=fundamental","pubTime":"2025-04-02 19:00","pubTimestamp":1743591600,"startTime":"0","endTime":"0","summary":"During the first 16 weeks of the Extension phase of the RewinD-LB clinical study neflamapimod slowed clinical progression compared to controls, as assessed by Clinical Dementia Rating Sum of Boxes  and Clinical Global Impression of Change . Neflamapimod was associated with a reduced incidence of falls in the Extension phase of the study and new data to be presented at AD/PD 2025 demonstrates improvements on endpoints measuring cognitive fluctuations and working memory. “The presentation of the Extension phase data at AD/PD 2025 is an opportunity to share our findings and engage deeply with the DLB medical community as we plan for pivotal development and work to bring neflamapimod to patients as rapidly as possible,” said John Alam, MD, Co-Principal Investigator of the RewinD-LB study and CEO of CervoMed. “The positive findings across the primary outcome measure and multiple additional clinically important endpoints evaluated in the first 16 weeks of the Extension phase strengthen our b","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://finance.yahoo.com/news/investigators-present-clinical-trial-results-110000131.html","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":"yahoofinance","symbols":["BK4023","BK4097","LU0240878834.USD","LU0348723411.USD","LU1169589451.USD","TUG","LU1169590202.USD","PD","LU0205194284.USD","LU0205193047.USD","LU0345774391.USD","LU0345774631.USD","CRVO","CGIC","LU0240877869.USD","BK4139","DLB"],"gpt_icon":0},{"id":"2524618914","title":"Vigil Neuroscience Presents Data on its Small Molecule TREM2 Agonist VG-3927 in Two Oral Presentations at AD/PD™ 2025 International Conference","url":"https://stock-news.laohu8.com/highlight/detail?id=2524618914","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524618914?lang=en_us&edition=fundamental","pubTime":"2025-04-02 19:00","pubTimestamp":1743591600,"startTime":"0","endTime":"0","summary":"- Preclinical presentation highlights key, modality specific, pharmacological differentiations of VG-3927 -- First presentation of topline clinical data from Phase 1 SAD/MAD trial of VG-3927 for the potential treatment of Alzheimer’s disease  -. WATERTOWN, Mass., April 02, 2025  -- Vigil Neuroscience, Inc. , a clinical-stage biotechnology company committed to harnessing the power of microglia for the treatment of neurodegenerative diseases, today presented data highlighting its oral small molecule program, including its lead clinical candidate VG-3927, in two oral presentations at the AD/PD 2025 International Conference on Alzheimer’s and Parkinson’s Diseases being held April 1 – April 5 in Vienna, Austria.Oral presentation by Christian Mirescu, Ph.D., Senior Vice President, Neuroimmunology: Small Molecule TREM2 Agonists as Next-Generation Therapeutics for Alzheimer’s DiseaseDate and Time: Wednesday, April 2, 2025, 3:20 PM – 3:35 PM Session: TREM2, Microglia: From Mechanisms to Potenti","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://finance.yahoo.com/news/vigil-neuroscience-presents-data-small-110000638.html","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":"yahoofinance","symbols":["PK","BK4023","BK4139","BK4213","PD","VIGL","LU1169590202.USD","PAM","LU1169589451.USD","CSF","VG","BK4181","BK4081","CET","BK4218","BK4563","ARIA"],"gpt_icon":0},{"id":"2524468300","title":"AC Immune Reports Further Positive Interim Results from Phase 2 Trial of ACI-7104.056 Active Immunotherapy in Early Parkinson’s Disease","url":"https://stock-news.laohu8.com/highlight/detail?id=2524468300","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524468300?lang=en_us&edition=fundamental","pubTime":"2025-04-02 18:00","pubTimestamp":1743588000,"startTime":"0","endTime":"0","summary":"AC Immune Reports Further Positive Interim Results from Phase 2 Trial of ACI-7104.056 Active Immunotherapy in Early Parkinson’s Disease. Active immunotherapy with ACI-7104.056 induces high anti-a-synuclein  antibody levels on average over 20-fold higher than placebo after 4 immunizations. Repeated immunizations amplify the anti-a-syn antibody response, supporting boostability and the potential to further increase antibody titers. ACI-7104.056 is well tolerated with no safety issues reported to date. Lausanne, Switzerland, April 2, 2025 – AC Immune SA , a clinical-stage biopharmaceutical company pioneering precision therapeutics for neurodegenerative diseases, today announced additional interim safety and positive immunogenicity data from the Phase 2 VacSYn clinical trial evaluating ACI-7104.056, its wholly owned anti-alpha-synuclein  active immunotherapy candidate, for the treatment of patients with early Parkinson’s disease .Interim results show positive antibody responses were effect","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://finance.yahoo.com/news/ac-immune-reports-further-positive-100000259.html","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":"yahoofinance","symbols":["LU1169590202.USD","ACI","LU1169589451.USD","BK4023","BK4139","ACIU","AC","BK4135","PD","BK4113"],"gpt_icon":0},{"id":"2524124280","title":"PagerDuty Report Finds More Than Half of Companies Have Deployed AI Agents","url":"https://stock-news.laohu8.com/highlight/detail?id=2524124280","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524124280?lang=en_us&edition=fundamental","pubTime":"2025-04-02 04:30","pubTimestamp":1743539400,"startTime":"0","endTime":"0","summary":"By 2027, 86% of companies expect to be operational with AI agents.Executives anticipate agentic AI will have faster adoption and higher ROI than generative AI, with 62% expecting returns above 100%. Leaders expect nearly 40% of work to be automated or expedited with the help of AI agents. To read the full report, including survey findings and methodology, please visit here.The adoption of GenAI has surged, with McKinsey & Company reporting usage in at least one business function rising from 33% in 2023 to 71% by July 2024. Now, agentic AI adoption is poised to accelerate even faster while reshaping automation and decision-making across industries. Companies are no longer just experimenting. The latest PagerDuty survey data shows that 94% of companies believe they will adopt agentic AI more quickly than GenAI, with 55% strongly agreeing that they will integrate it across their organizations at an accelerated pace. As businesses look to automate complex workflows and drive efficiency, ag","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://finance.yahoo.com/news/pagerduty-report-finds-more-half-203000686.html","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":"yahoofinance","symbols":["LU1169590202.USD","PD","BK4023","LU1169589451.USD"],"gpt_icon":0},{"id":"2524113865","title":"Cerevance Presents Topline Results from Phase 2 ASCEND Trial of Solengepras as Monotherapy Treatment for Early-Stage Parkinson’s Disease at AD/PD 2025","url":"https://stock-news.laohu8.com/highlight/detail?id=2524113865","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524113865?lang=en_us&edition=fundamental","pubTime":"2025-04-01 20:15","pubTimestamp":1743509700,"startTime":"0","endTime":"0","summary":"Solengepras showed evidence of potential benefit in functional and non-motor symptoms versus placebo as measured by MDS-UPRDS Parts I, II, NMSS, and ESS, consistent with its novel non-dopaminergic mec","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.globenewswire.com/news-release/2025/04/01/3053340/0/en/Cerevance-Presents-Topline-Results-from-Phase-2-ASCEND-Trial-of-Solengepras-as-Monotherapy-Treatment-for-Early-Stage-Parkinson-s-Disease-at-AD-PD-2025.html","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":["ESS","BK4588","BK4023","LU1169590202.USD","SSI","BK4215","BK4597","BK4585","LU1169589451.USD","PD"],"gpt_icon":0},{"id":"2524519419","title":"Aquestive Therapeutics Announces Positive Topline PK Results from its Pediatric Study and Completes the NDA Submission for Anaphylm™ (epinephrine) Sublingual Film","url":"https://stock-news.laohu8.com/highlight/detail?id=2524519419","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524519419?lang=en_us&edition=fundamental","pubTime":"2025-04-01 19:00","pubTimestamp":1743505200,"startTime":"0","endTime":"0","summary":"Reports positive pharmacokinetic (PK) results from the recently completed pediatric study for Anaphylm Completes submission of its New Drug Application (NDA) for Anaphylm to the FDA; NDA acceptance ex","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://www.globenewswire.com/news-release/2025/04/01/3053173/0/en/Aquestive-Therapeutics-Announces-Positive-Topline-PK-Results-from-its-Pediatric-Study-and-Completes-the-NDA-Submission-for-Anaphylm-epinephrine-Sublingual-Film.html","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":["BK4181","PD","PK","BK4139","AQST","LU1169590202.USD","BK4218","BK4007","LENZ","BK4023","LU1169589451.USD"],"gpt_icon":0},{"id":"2524194196","title":"Tovecimig (CTX-009) Meets Primary Endpoint in the Ongoing Randomized Phase 2/3 Study in Patients with Biliary Tract Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2524194196","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524194196?lang=en_us&edition=fundamental","pubTime":"2025-04-01 19:00","pubTimestamp":1743505200,"startTime":"0","endTime":"0","summary":"Tovecimig (a DLL4 x VEGF-A bispecific antibody) in combination with paclitaxel achieved a 17.1% overall response rate (ORR), including one complete response, compared to 5.3% ORR for paclitaxel alone,","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.globenewswire.com/news-release/2025/04/01/3053162/0/en/Tovecimig-CTX-009-Meets-Primary-Endpoint-in-the-Ongoing-Randomized-Phase-2-3-Study-in-Patients-with-Biliary-Tract-Cancer.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CMPX","BK4211","BTC","IE00B19Z3B42.SGD","BK4161","CR","IE0002270589.USD","BK4023","BK4092","BK4213","PD","IE00B7SZLL34.SGD","LU1169590202.USD","BK4097","LU1169589451.USD","ORR","PR","OS","BK4195","PFS","IE00B19Z3581.USD","SD","NE","BK4139"],"gpt_icon":0},{"id":"2524134775","title":"Quanterix Showcases Innovation Powered by Simoa® at AD/PD with Customer Research and New Dried Blood Spot Extraction Kit","url":"https://stock-news.laohu8.com/highlight/detail?id=2524134775","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524134775?lang=en_us&edition=fundamental","pubTime":"2025-04-01 13:00","pubTimestamp":1743483600,"startTime":"0","endTime":"0","summary":"Simoa technology highlighted in more than 80 posters and oral presentations demonstrating its impact on neurodegenerative disease research. BILLERICA, Mass., April 01, 2025----Quanterix Corporation , a company fueling scientific discovery through ultrasensitive biomarker detection, today announced the inclusion of a new dried blood spot extraction  kit as part of their industry-leading Simoa assay kits at the International Conference on Alzheimer’s and Parkinson’s Diseases and Related Neurological Disorders  in Vienna, Austria. This new extraction kit enables researchers to measure low-concentration biomarkers from dried blood spots using a more cost-effective and less invasive method.From discovery to diagnostics, Quanterix’s ultrasensitive biomarker detection is fueling breakthroughs only made possible through its unparalleled sensitivity and flexibility. The Company’s Simoa technology has delivered the gold standard for earlier biomarker detection in blood, serum or plasma, with the","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://finance.yahoo.com/news/quanterix-showcases-innovation-powered-simoa-050000940.html","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":"yahoofinance","symbols":["BK4121","LU1169590202.USD","BK4023","PD","LU1169589451.USD","QTRX","DBS"],"gpt_icon":0},{"id":"2523917896","title":"ProMIS Neurosciences Announces Full Year 2024 Financial Results and Recent Highlights","url":"https://stock-news.laohu8.com/highlight/detail?id=2523917896","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2523917896?lang=en_us&edition=fundamental","pubTime":"2025-03-31 19:00","pubTimestamp":1743418800,"startTime":"0","endTime":"0","summary":"Rapid Enrollment and Dosing of First Patients in PRECISE-AD Trial Underscores the Unmet Need for Better Treatment Options for Alzheimer’s Disease. PRECISE-AD Six Month Interim Results Expected in 1H 2026 with Topline Results Anticipated by end of 2026. CAMBRIDGE, Massachusetts, March 31, 2025  -- ProMIS Neurosciences Inc. , a clinical-stage biotechnology company focused on the generation and development of antibody therapeutics targeting toxic misfolded proteins in neurodegenerative diseases, such as Alzheimer’s disease , amyotrophic lateral sclerosis  and multiple system atrophy , today announced financial results for the fiscal year ended December 31, 2024 and provided a corporate update.Based on the encouraging results from the Phase 1a study of PMN310, ProMIS initiated a","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://finance.yahoo.com/news/promis-neurosciences-announces-full-2024-110000013.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BK4023","IP","LU2125909759.SGD","PD","IE00B3T34201.USD","LU1481599808.USD","LU1923622291.USD","LU1481600234.SGD","LU0757428866.USD","BK4139","LU1169589451.USD","MSA","LU2211815571.USD","LU1815336091.USD","PK","BK4136","BK4585","LU1169590202.USD","BK4143","LU1487256676.USD","LU0053671581.USD","LU2125909916.SGD","PMN","BK4588","LU0728928796.USD","BK4178","BK4218","BK4181","LU2463526074.USD","AAN","PIPE"],"gpt_icon":0},{"id":"2523917675","title":"Voyager Presents Robust Preclinical Data from Tau Targeting Gene Therapy and Antibody Programs at AD/PD™ 2025","url":"https://stock-news.laohu8.com/highlight/detail?id=2523917675","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2523917675?lang=en_us&edition=fundamental","pubTime":"2025-03-31 19:00","pubTimestamp":1743418800,"startTime":"0","endTime":"0","summary":"- Single IV administration of tau silencing gene therapy VY1706 significantly reduced tau mRNA and protein levels, with broad brain distribution and liver de-targeting, in NHP study - - Preclinical mu","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.globenewswire.com/news-release/2025/03/31/3052163/36461/en/Voyager-Presents-Robust-Preclinical-Data-from-Tau-Targeting-Gene-Therapy-and-Antibody-Programs-at-AD-PD-2025.html","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":["PD","LU1169589451.USD","LU1169590202.USD","BK4192","PET","BK4023","CTA"],"gpt_icon":0},{"id":"2523579917","title":"Vaxcyte Announces Positive Topline Results from VAX-24 Infant Phase 2 Dose-Finding Study","url":"https://stock-news.laohu8.com/highlight/detail?id=2523579917","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2523579917?lang=en_us&edition=fundamental","pubTime":"2025-03-31 19:00","pubTimestamp":1743418800,"startTime":"0","endTime":"0","summary":"-- At All Doses Evaluated, VAX-24 Was Well-Tolerated and Demonstrated a Safety and Tolerability Profile Similar to Prevnar 20 (PCV20)-- -- At All Doses Evaluated, VAX-24 Elicited Substantial Immune Re","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://www.globenewswire.com/news-release/2025/03/31/3052157/0/en/Vaxcyte-Announces-Positive-Topline-Results-from-VAX-24-Infant-Phase-2-Dose-Finding-Study.html","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":["BK4208","PD","BK4585","NI","PCVX","BK4588","LU1169589451.USD","BK4023","LU0053671581.USD","LU1169590202.USD","IE0009354923.USD","BK4139"],"gpt_icon":0},{"id":"2522520587","title":"Press Release: LAVA Reports Fourth Quarter and Full Year 2024 Financial Results and Provides a Business Update","url":"https://stock-news.laohu8.com/highlight/detail?id=2522520587","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2522520587?lang=en_us&edition=fundamental","pubTime":"2025-03-28 19:30","pubTimestamp":1743161400,"startTime":"0","endTime":"0","summary":"-- Focused on the evaluation of strategic alternatives. -- Adopted a restructuring plan to extend capital resources, incurring a. reduction in workforce of 30% to support the evaluation of strategic. -- Phase 1 enrollment in LAVA-1266 clinical trial underway. \"LAVA's approach to maximize shareholder value in 2025 will focus on evaluating strategic options while continuing to enroll patients in our ongoing Phase 1 study of LAVA-1266, and supporting our pharma partnerships,\" said Steve Hurly, Chief Executive Officer of LAVA. \"The Phase 1 study of LAVA-1266 as a potential treatment for acute myeloid leukemia and myelodysplastic syndrome is progressing. Looking ahead, with a strong cash balance, we believe LAVA is well-positioned to unlock strategic opportunities, and we look forward to updating investors with our progress throughout the year.\". Designed to target CD123+ tumor cells for the treatment of hematological malignancies. -- Current Status: LAVA is enrolling patients in the second","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":["CRC","LU0122379950.USD","LU0203345920.USD","IE00BVYPNV92.GBP","LU0058720904.USD","LU1280957306.USD","LU1732799900.SGD","LU1674673428.USD","LU2347655156.SGD","IE00B2B36J28.USD","IE0034235303.USD","LU0882574055.USD","SG9999001176.SGD","SG9999002224.SGD","SG9999001176.USD","LU0170899867.USD","LU1883839398.USD","BK4588","BK4592","LU1778281490.HKD","SG9999011175.SGD","LU2592432038.USD","LU2468319806.SGD","SGXZ57979304.SGD","R","LU1914381329.SGD","PD","PK","LU1894683264.USD","LU2430703095.HKD","LU0466842654.USD","LU2112291526.USD","LU0234570918.USD","BK4534","LU1061106388.HKD","BK4023","SG9999002232.USD","BK4213","LU1066053197.SGD","LVTX","JNJ","LU1032466523.USD","LU1674673691.USD","LU1267930813.SGD","LU1059921491.USD","LU0320765646.SGD","BK4504","LU1032955483.USD","LU0306807586.USD"],"gpt_icon":1},{"id":"2522532085","title":"TransCode Therapeutics Announces Initial Dosing in Fourth Cohort of Phase 1 Clinical Trial with TTX-MC138","url":"https://stock-news.laohu8.com/highlight/detail?id=2522532085","media":"PR Newswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2522532085?lang=en_us&edition=fundamental","pubTime":"2025-03-28 04:37","pubTimestamp":1743107820,"startTime":"0","endTime":"0","summary":"First patient in Cohort four has been treated with TTX-MC138. Ten patients have been treated with TTX-MC138 at escalating dose levels. \"Commencement of treatment in Cohort 4 has been our vision for evaluating the potential of TTX-MC138 at multiple dose levels. Cohort 4 builds upon our safety, PK/PD and exploratory data and is an important element of our clinical development strategy. We believe this milestone will inform the dose expansion stage of the clinical trial and may allow us to obtain initial evidence of clinical activity as the program continues to advance,\" commented SueDuggan, TransCode's Senior Vice President of Operations. Duggan added, \"Enrollment into the study continues based on the cumulative safety data review. Additional Cohort 4 patients are scheduled for treatment in Cohort 4 for treatment with TTX-MC138 while preliminary data analysis continues.\". TTX-MC138 is a first-in-class therapeutic candidate that targets microRNA-10b, a micro-RNA widely believed to be a dr","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"yahoofinance","url":"https://finance.yahoo.com/news/transcode-therapeutics-announces-initial-dosing-203700928.html","rn_cache_url":null,"customStyle":"img, svg { display: none !important; }","selectors":"article","filters":"","directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/transcode-therapeutics-announces-initial-dosing-203700928.html","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":"yahoofinance","symbols":["PK","RNAZ","LU1169590202.USD","BK4218","BK4023","BK4181","BK4539","LENZ","BK4139","LU1169589451.USD","PD"],"gpt_icon":1},{"id":"2522344545","title":"Annovis Bio, Inc. Receives Continued Listing Standard Notice From the NYSE","url":"https://stock-news.laohu8.com/highlight/detail?id=2522344545","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2522344545?lang=en_us&edition=fundamental","pubTime":"2025-03-28 04:30","pubTimestamp":1743107400,"startTime":"0","endTime":"0","summary":"MALVERN, Pa., March 27, 2025  -- Annovis Bio, Inc.  , a late-stage clinical drug platform company pioneering transformative therapies for neurodegenerative diseases such as Alzheimer’s disease  and Parkinson’s disease , today announced that on March 26, 2025, it received notice  from the New York Stock Exchange  that it is no longer in compliance with the NYSE continued listing standards set forth in Section 802.01B of the NYSE’s Listed Company Manual due to the fact that the Company’s average global market capitalization over a consecutive 30 trading-day period was less than $50 million while its stockholders’ equity was less than $50 million.The Notice does not affect the Company’s business operations or its reporting obligations with the Securities and Exchange Commission, and it does not conflict with or cause an event of default under any of the Company’s material debt or other agreements.Cautionary Note Regarding Forward-Looking StatementsThis press release contains, and oral sta","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://finance.yahoo.com/news/annovis-bio-inc-receives-continued-203000438.html","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":"yahoofinance","symbols":["BK4124","LU1169590202.USD","BK4023","NYSE","BK4139","ANVS","LU1169589451.USD","PD","SMP"],"gpt_icon":0},{"id":"2522558078","title":"Sensei Biotherapeutics Reports Favorable Preliminary Dose Expansion Data for Solnerstotug in PD-(L)1 Resistant Tumors","url":"https://stock-news.laohu8.com/highlight/detail?id=2522558078","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2522558078?lang=en_us&edition=fundamental","pubTime":"2025-03-28 04:05","pubTimestamp":1743105900,"startTime":"0","endTime":"0","summary":"– Initial clinical activity in a PD-1 resistant population, with an ORR almost three times higher than historical PD-1 rechallenge response rates, with data still maturing –。– One durable complete response in a Merkel Cell Carcinoma  patient and two partial responses , including one in a second MCC patient and one in a microsatellite instability-high  Colorectal Cancer  patient, all of whom were previously treated with and progressed on immunotherapy –。– All PD-1 resistant “hot” tumor patients with tumor shrinkage remain on study, suggesting potential for deepening responses over time –。The Phase 1 dose expansion trial is a multi-center, open-label, dose expansion study evaluating solnerstotug as monotherapy and in combination withLibtayo , Regeneron’s PD-1 inhibitor, in both a basket of “hot” tumorsthat typically respond to immunotherapy but have progressed on prior PD-1 therapy and a single “cold” tumor histology  that is typically unresponsive to immunotherapy.At the time of this 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