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PagerDuty, Inc.

16.07

-0.2700-1.65%

Post-market: 16.070.00000.00%16:20 EDT

Volume:1.39M

Turnover:22.35M

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

PagerDuty Inc: Expanding Size of Its Board to Ten

THOMSON REUTERS

PagerDuty Inc - Donald J. Carty Appointed to PagerDuty Board

THOMSON REUTERS

PagerDuty Inc - Enters Cooperation Agreement With Scalar Gauge Fund

THOMSON REUTERS

PagerDuty Appoints New Member to Board of Directors in Collaboration With Scalar Gauge Fund

THOMSON REUTERS

PagerDuty Appoints New Member to Board of Directors in Collaboration with Scalar Gauge Fund

New to The Street Airs on Bloomberg TV Saturday, April 26 at 6:30 PM ET Featuring BioVie (NASDAQ: BIVI), Skip Barber Racing School with CFO Michael Berg, CommercialVille.tv, Sustainable Green Team (OTCPK: SGTM) WaterLess Garden, and The Business of Blockchain with Michael Casey

ACCESS Newswire

Pasithea Therapeutics to Present Updated Data from Ongoing Phase 1 Trial of PAS-004 in Advanced Cancer Patients at the 2025 ASCO Annual Meeting

Ivonescimab in Combination with Chemotherapy Achieves Statistically Significant Superiority in PFS vs. Tislelizumab (PD-1 Inhibitor) Plus Chemotherapy in 1L Treatment of Patients with Squamous NSCLC in HARMONi-6 Study Conducted by Akeso in China

Trodelvy® Plus Keytruda® Demonstrates a Statistically Significant and Clinically Meaningful Improvement in Progression Free Survival in Patients With Previously Untreated PD-L1+ Metastatic Triple-Negative Breast Cancer

BioVie Initiates SUNRISE-PD Clinical Trial Assessing Bezisterim in Early Parkinson’s Disease with First Patient Enrolled

Galmed Unveils Novel Pharmacodynamic Blood Markers for Aramchol, the Most Clinically Advanced SCD1 Inhibitor

MetaVia Announces Positive Top-Line Data From the 4-Week Phase 1 MAD Trial of DA-1726, a Novel 3:1 Ratio GLP-1 Glucagon Dual Receptor Agonist to Treat Obesity, Showing Compelling Weight Loss and Safety Effects With Potential Best-In-Class Glucose Control (GLP-1R), Waist Reduction (GCGR), and Tolerability

Verve Therapeutics Announces Positive Initial Data from the Heart-2 Phase 1b Clinical Trial of VERVE-102, an In Vivo Base Editing Medicine Targeting PCSK9

Pasithea Therapeutics Announces Positive Safety Review Committee (SRC) Recommendation from its Ongoing Phase 1 Clinical Trial of PAS-004 in Advanced Cancer

Gain Therapeutics Presents Additional Preclinical Data and Design of Phase 1b Clinical Study of GT-02287 at AD/PD 2025 and Provides Enrollment Update

PagerDuty Named a Leader and Outperformer in GigaOm Radar for IT Incident Response Platforms for Third Consecutive Year

Verizon Frontline provides critical Unmanned Aircraft Systems support for New Orleans PD during Mardi Gras

NKGen Biotech Presents Data from Phase 1/2a Clinical Trial of Troculeucel in Moderate Alzheimer’s Disease at the International Conference on Alzheimer’s and Parkinson’s Diseases (AD/PD™ 2025)

Amneal Announces New Data from Phase 3 Study Showing Significant Improvements in Sleep Quality with CREXONT® (Carbidopa and Levodopa) Extended-Release Capsules in Parkinson’s Disease

Tharimmune Announces Positive Data with Novel Biparatopic PD-1/VEGF and Multispecific HER2/HER3 Biologics Leveraging Proprietary EpiClick(TM) Technology

ACCESS Newswire

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Donald J. Carty currently serves as Chairman of Porter Airlines, a privately held Canada-based airline. Carty previously served as Chairman and CEO of AMR Corporation and American Airlines, President and Chief Executive Officer of Canadian Pacific Air Lines and Vice Chairman and Chief Financial Officer of Dell. Carty also has decades of experience as a public company board member, previously serving as Chairman of the Virgin America Board, and as a director on the boards of VMware, Hawaiian Airlines,","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-appoints-member-board-directors-130000213.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["LU1169589451.USD","BK4023","PD","LU1169590202.USD"],"gpt_icon":0},{"id":"2530150557","title":"New to The Street Airs on Bloomberg TV Saturday, April 26 at 6:30 PM ET Featuring BioVie (NASDAQ: BIVI), Skip Barber Racing School with CFO Michael Berg, CommercialVille.tv, Sustainable Green Team (OTCPK: SGTM) WaterLess Garden, and The Business of Blockchain with Michael Casey","url":"https://stock-news.laohu8.com/highlight/detail?id=2530150557","media":"ACCESS Newswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530150557?lang=en_us&edition=fundamental","pubTime":"2025-04-26 00:45","pubTimestamp":1745599500,"startTime":"0","endTime":"0","summary":"NEW YORK CITY, NEW YORK / ACCESS Newswire / April 25, 2025 / New to The Street, the nation's longest-running business television series dedicated to emerging innovation and investor awareness, will air Episode #651 on Bloomberg Television this Saturday, April 26 at 6:30 PM ET. This episode features visionary leaders and technologies across biotech, motorsport education, blockchain, sustainable infrastructure, and small business marketing.BioVie is pioneering treatments for Alzheimer's disease , Parkinson's disease , and long COVID with its lead drug candidate Bezisterim  - a brain-penetrating, anti-inflammatory insulin sensitizer with promising clinical results in cognition and motor improvement.Skip Barber Racing School - Featuring CFO Michael Berg. Michael Berg, CFO of Skip Barber Racing School, discusses the company's future and enduring legacy as the gold standard in American motorsport education. With over 45 years of history, the brand is now expanding its reach with new programs","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/street-airs-bloomberg-tv-saturday-164500213.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":["LU2210149790.SGD","TV","BK4112","BK4588","ET",".IXIC","BIVI","BK4139","IE00B3QW5Z07.USD","BK4581","BK4100","PD","LU2210150020.SGD","BK4120","IE00BGHQF748.EUR","LU1169589451.USD","SGTM","NDAQ","BK4561","IE00BKPKM429.USD","BK4585","BK4144","LU2095319765.USD","IE00B64PRP62.GBP","LU1169590202.USD","BK4023","BK4590"],"gpt_icon":0},{"id":"2529607368","title":"Pasithea Therapeutics to Present Updated Data from Ongoing Phase 1 Trial of PAS-004 in Advanced Cancer Patients at the 2025 ASCO Annual Meeting","url":"https://stock-news.laohu8.com/highlight/detail?id=2529607368","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529607368?lang=en_us&edition=fundamental","pubTime":"2025-04-24 19:02","pubTimestamp":1745492520,"startTime":"0","endTime":"0","summary":"Poster presentation on Monday, June 2, 2025 from 1:30 – 4:30 PM CDT at the ASCO Annual Meeting. MIAMI, April 24, 2025  -- Pasithea Therapeutics Corp.  , a clinical-stage biotechnology company developing PAS-004, a next-generation macrocyclic MEK inhibitor, for the treatment of neurofibromatosis type 1  and other MAPK pathway driven indications, today announced the acceptance of an abstract for a poster prenstation at the Annual Meeting of the American Society for Clinical Oncology  taking place May 30 – June 3, 2025, in Chicago, Illinois.The Company will present updated interim clinical data from its onging Phase 1 clinical trial of PAS-004 in patients with MAPK pathway driven advanced solid tumors.","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/pasithea-therapeutics-present-updated-data-110200343.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":["IE00B7SZL793.SGD","IE0031619046.USD","IE00B19Z4B17.USD","LU1169589451.USD","BK4157","PK","BK4007","LU1169590202.USD","AEIS","BK4023","BK4181","BK4139","IE00B66KJ199.SGD","KTTA","BK4135","LENZ","PD","BK4218","KTTAW","CNS"],"gpt_icon":0},{"id":"2529150898","title":"Ivonescimab in Combination with Chemotherapy Achieves Statistically Significant Superiority in PFS vs. Tislelizumab (PD-1 Inhibitor) Plus Chemotherapy in 1L Treatment of Patients with Squamous NSCLC in HARMONi-6 Study Conducted by Akeso in China","url":"https://stock-news.laohu8.com/highlight/detail?id=2529150898","media":"Business Wire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529150898?lang=en_us&edition=fundamental","pubTime":"2025-04-23 18:15","pubTimestamp":1745403300,"startTime":"0","endTime":"0","summary":"Ivonescimab in Combination with Chemotherapy in the HARMONi-6 Study Conducted by Akeso Is the First Known Regimen to Achieve a Clinically Meaningful Benefit over an anti-PD-1 Antibody Combined with Chemotherapy in a Phase III Clinical Trial in 1L NSCLC. PFS Improvement Was Observed across Tumors with PD-L1 Negative and PD-L1 Positive Expression in the HARMONi-6 Clinical Trial Conducted by Akeso. Full Data Set to be Presented at an Upcoming Major Medical Conference Planned for Later This Year. At a prespecified interim analysis conducted by an Independent Data Monitoring Committee, ivonescimab plus chemotherapy demonstrated a statistically significant and clinically meaningful improvement in PFS by blinded independent central radiology review committee  compared to tislelizumab plus chemotherapy. The PFS benefit was demonstrated in patients with either PD-L1-positive or PD-L1-negative tumors. Akeso noted that no new safety signals were identified in this Phase III study. The full data s","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/ivonescimab-combination-chemotherapy-achieves-statistically-101500586.html","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":"yahoofinance","symbols":["L","BK4565","IE00BYQNZ168.SGD","BK4139","BK4023","IE00B12V2V27.USD","IE00BYTNYN87.SGD","PD","BK4548","BK4588","PFS","BK4526","LU1169589451.USD","BK4571","BK4531","LU0053666078.USD","BK4563","BK4108","BK4585","BK4509","LU1023057109.AUD","LU2039709279.SGD","01698","SMMT","TME","BK4552","BK4211","LU0359202008.SGD","LU1169590202.USD","BK4195","LU0359201612.USD","LU2488822045.USD","BK4535","SG9999011746.SGD","BK4107"],"gpt_icon":0},{"id":"2529689806","title":"Trodelvy® Plus Keytruda® Demonstrates a Statistically Significant and Clinically Meaningful Improvement in Progression Free Survival in Patients With Previously Untreated PD-L1+ Metastatic Triple-Negative Breast Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2529689806","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529689806?lang=en_us&edition=fundamental","pubTime":"2025-04-21 20:30","pubTimestamp":1745238600,"startTime":"0","endTime":"0","summary":"– The First Pivotal Phase 3 Trial to Demonstrate Superiority of a TROP-2 Antibody-Drug Conjugate, Trodelvy, Plus Keytruda Versus Standard of Care Keytruda plus Chemotherapy in 1L mTNBC –。– Trodelvy Plus Keytruda Shows an Early Trend in Improvement for Overall Survival Versus Standard of Care in Patients with Previously Untreated PD-L1+  mTNBC –。\"These findings are the first to show the transformative potential of an antibody-drug conjugate combined with an immuno-oncology agent in early treatment lines of metastatic breast cancer,\" said Dietmar Berger, MD, PhD, Chief Medical Officer, Gilead Sciences. \"For patients with this difficult to treat type of breast cancer, these results potentially offer a new pathway that may redefine their treatment options.\". The significant and meaningful improvement in PFS demonstrated in ASCENT-04 further reinforces the potential of Trodelvy plus Keytruda as a much-needed new treatment option for patients with previously untreated inoperable  PD-L1+ loca","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/trodelvy-plus-keytruda-demonstrates-statistically-123000256.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["LU0208291251.USD","LU1023059063.AUD","IE00BSNM7G36.USD","IE00B1BXHZ80.USD","LU0234570918.USD","LU1162221912.USD","IE00BJT1NW94.SGD","LU2087621335.USD","LU0106261372.USD","BK4585","IE00BKVL7J92.USD","LU0965509283.SGD","IE00BZ1G4Q59.USD","LU0203347892.USD","GILD","LU0861579265.USD","LU0965508806.USD","LU0985320562.USD","LU0109394709.USD","SG9999002232.USD","ORR","LU0265550359.USD","LU2023250843.SGD","IE000M9KFDE8.USD","MCBS","SG9999002224.SGD","LU1585245621.USD","LU0234572021.USD","LU1035773651.USD","SG9999001176.USD","PFS","HR","LU1069347547.HKD","SAR","MRK","BK4578","SG9999014542.SGD","ADC","LU1093756325.SGD","LU2112291526.USD","LU1066051225.USD","LU2361045086.USD","BK4007","CINV","OS","BK4203","IE00BBT3K403.USD","LU2106854487.HKD","PD","LU0203345920.USD"],"gpt_icon":0},{"id":"2527161522","title":"BioVie Initiates SUNRISE-PD Clinical Trial Assessing Bezisterim in Early Parkinson’s Disease with First Patient Enrolled","url":"https://stock-news.laohu8.com/highlight/detail?id=2527161522","media":"GlobeNewswire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527161522?lang=en_us&edition=fundamental","pubTime":"2025-04-16 20:00","pubTimestamp":1744804800,"startTime":"0","endTime":"0","summary":"SUNRISE-PD evaluating the Company’s anti-inflammatory, insulin-sensitizing candidate bezisterim in patients with Parkinson’s disease who have not been treated with carbidopa/levodopa. SUNRISE-PD is one of very few clinical trials for a Parkinson’s disease treatment to incorporate a decentralized approach option to allow for remote participation. Patient enrollment has commenced, with recruitment being supported by The Michael J. Fox Foundation, Davis Phinney Foundation and The Parkinson’s Foundation. Topline data anticipated in Late 2025 or Early 2026. SUNRISE-PD is a Phase 2b, multicenter, randomized, double-blind, placebo-controlled trial with a hybrid decentralized design that will last 20 weeks from the initial screening phase to the safety follow up. During the 12-week double-blind phase, approximately 60 patients will be randomized 1:1 to receive either 20 mg of bezisterim or pla","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/biovie-initiates-sunrise-pd-clinical-120000103.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":["LU1169589451.USD","BK4139","LU1169590202.USD","PD","BIVI","BK4023"],"gpt_icon":0},{"id":"2527415023","title":"Galmed Unveils Novel Pharmacodynamic Blood Markers for Aramchol, the Most Clinically Advanced SCD1 Inhibitor","url":"https://stock-news.laohu8.com/highlight/detail?id=2527415023","media":"PR Newswire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527415023?lang=en_us&edition=fundamental","pubTime":"2025-04-15 20:30","pubTimestamp":1744720200,"startTime":"0","endTime":"0","summary":"Analysis of blood samples from patients treated withAramchol in ARMOR  provides new and important insights into the biochemical and physiological effects of the drug.The pharmacodynamic signature associated with Aramchol treatment revealed a decrease in markers of chronic systemic inflammation, oxidative and cardiac stress, and atherosclerotic plaque pathogenesis.TEL AVIV, Israel, April 15, 2025 /PRNewswire/ --Galmed Pharmaceuticals Ltd.  , a clinical-stage biopharmaceutical company dedicated to developing novel treatments for liver, cardiometabolic, and gastrointestinal oncology indications, today announces the unveiling of novel pharmacodynamic  blood markers for its lead compound, Aramchol, the industry's most clinically advanced SCD1 inhibitor. These newly identified biomarkers shed fresh light on Aramchol's potential far beyond its role in NASH  therapy—offering a deeper understanding of the drug candidate's biochemical impact and presenting an exciting opportunity to enhance clin","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"yahoofinance","url":"https://finance.yahoo.com/news/galmed-unveils-novel-pharmacodynamic-blood-123000723.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/galmed-unveils-novel-pharmacodynamic-blood-123000723.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":["LU1169590202.USD","PD","GLMD","AEIS","BK4023","IE0031619046.USD","IE00B7SZL793.SGD","BK4157","IE00B19Z4B17.USD","BK4139","IE00B66KJ199.SGD","LU1169589451.USD"],"gpt_icon":0},{"id":"2527492780","title":"MetaVia Announces Positive Top-Line Data From the 4-Week Phase 1 MAD Trial of DA-1726, a Novel 3:1 Ratio GLP-1 Glucagon Dual Receptor Agonist to Treat Obesity, Showing Compelling Weight Loss and Safety Effects With Potential Best-In-Class Glucose Control (GLP-1R), Waist Reduction (GCGR), and Tolerability","url":"https://stock-news.laohu8.com/highlight/detail?id=2527492780","media":"PR Newswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527492780?lang=en_us&edition=fundamental","pubTime":"2025-04-15 19:01","pubTimestamp":1744714860,"startTime":"0","endTime":"0","summary":"With No Titration, Demonstrated Compelling Maximum Weight Loss of 6.3% andMean Weight Loss of 4.3% at Day 26 at 32 mg Dose . Demonstrated Strong Signal of GLP-1R Efficacy with Maximum Lowering of Fasted Glucose of -18 mg/dLand Mean Lowering of -5.3 mg/dL at Day 26 at 32 mg Dose. Maximum Waist Circumference Reduction of3.9 Inches and Mean Reduction of 1.6 InchesDemonstrates Strong Signal ofGlucagon Efficacy at Day 33 at 32 mg Dose. Additional Cohorts Being Added to Determine Maximum Tolerated Dose. Planned Phase 1 Part 3 to Include Wegovy Early Drop-Out Patients to Explore Potential Superiority of DA-1726 on Safety and Tolerability, Along With Weight Loss and Other Secondary Endpoints. CAMBRIDGE, Mass., April 15, 2025 /PRNewswire/ -- MetaVia Inc. ,a clinical-stage biotechnology company focused on transforming cardiometabolic diseases, today announced positive results from the 4-week multiple ascending dose  Part 2 of its Phase 1 clinical trial of DA-1726, a novel, dual oxyntomodulin  an","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"yahoofinance","url":"https://finance.yahoo.com/news/metavia-announces-positive-top-line-110100485.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/metavia-announces-positive-top-line-110100485.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":["MTVA","BK4218","BK4144","PD","BK4157","BK4139","BK4202","BK4590","LU1169589451.USD","OXM","GLP","LU1169590202.USD","PK","BMI","BK4181","BK4023"],"gpt_icon":0},{"id":"2527533581","title":"Verve Therapeutics Announces Positive Initial Data from the Heart-2 Phase 1b Clinical Trial of VERVE-102, an In Vivo Base Editing Medicine Targeting PCSK9","url":"https://stock-news.laohu8.com/highlight/detail?id=2527533581","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527533581?lang=en_us&edition=fundamental","pubTime":"2025-04-14 19:00","pubTimestamp":1744628400,"startTime":"0","endTime":"0","summary":"Single infusion of VERVE-102 led to dose-dependent decreases in blood PCSK9 and LDL-C, with mean reduction in LDL-C of 53% and a maximum reduction of 69% observed in the 0.6 mg/kg dose cohort VERVE-10","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/2025/04/14/3060774/0/en/Verve-Therapeutics-Announces-Positive-Initial-Data-from-the-Heart-2-Phase-1b-Clinical-Trial-of-VERVE-102-an-In-Vivo-Base-Editing-Medicine-Targeting-PCSK9.html","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":null,"symbols":["LU1169589451.USD","BK4539","LU1878469433.USD","BK4139","BK4599","BK4505","BK4585","LU1169590202.USD","PD","RNA","VERV","BK4023","BK4588","ALT"],"gpt_icon":0},{"id":"2526255278","title":"Pasithea Therapeutics Announces Positive Safety Review Committee (SRC) Recommendation from its Ongoing Phase 1 Clinical Trial of PAS-004 in Advanced Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2526255278","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2526255278?lang=en_us&edition=fundamental","pubTime":"2025-04-10 19:02","pubTimestamp":1744282920,"startTime":"0","endTime":"0","summary":"–SRC recommended that the trial escalate to the next dose level of 30mg capsule –。“We are seeing substantial enrollment demand and have already identified Cohort 6 patients. In addition, we continue to observe substantial exposure levels of PAS-004, and remain excited about the possibility of delivering relevant pERK inhibition below the no observed adverse effect levels  as we modeled and observed during our previously conducted nine-month chronic toxicity studies. The on label rash rate for both approved MEKi for NF1 exceeds 80% which leads to patients discontinuing who otherwise should remain on treatment for longer periods of time”, stated Dr. Tiago Reis Marques, Chief Executive Officer of Pasithea. “We will provide additional safety, pharmacokinetic  and pharmacodynamic  data over the next several weeks.”This press release contains statements that constitute “forward-looking statements” made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Ac","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/pasithea-therapeutics-announces-positive-safety-110200309.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":["BK4231","LU1169589451.USD","BK4181","LU1169590202.USD","PD","BK4157","BK4023","IE00B66KJ199.SGD","BK4218","BK4139","BK4007","SRC","IE00B7SZL793.SGD","IE00B19Z4B17.USD","PK","AEIS","BK4135","IE0031619046.USD","BK4080","LENZ","CNS","KTTA","KTTAW"],"gpt_icon":0},{"id":"2526517485","title":"Gain Therapeutics Presents Additional Preclinical Data and Design of Phase 1b Clinical Study of GT-02287 at AD/PD 2025 and Provides Enrollment Update","url":"https://stock-news.laohu8.com/highlight/detail?id=2526517485","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2526517485?lang=en_us&edition=fundamental","pubTime":"2025-04-10 19:00","pubTimestamp":1744282800,"startTime":"0","endTime":"0","summary":"GT-02287 oral presentation demonstrates new evidence of disease-modifying capacity in GBA1 and idiopathic Parkinson’s disease models. Phase 1b study ongoing to assess safety, tolerability, pharmacokinetics, and pharmacodynamics of GT-02287 in people with Parkinson’s disease; biomarker analysis to be conducted in Q2 2025. Summary: In animal models of both GBA1 and idiopathic Parkinson’s disease, GT-02287 is able to rescue motor deficits and prevent the development of deficits in complex behaviors such as nesting. These effects persist even following withdrawal of the compound, suggesting a disease-modifying potential of GT-02287. The new preclinical data that were pres","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/gain-therapeutics-presents-additional-preclinical-110000583.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":"yahoofinance","symbols":["CSF","PD","BK4218","BK4588","LU1169590202.USD","BK4119","BK4007","GT","BK4181","GANX","PK","LU1169589451.USD","LENZ","BK4139","BK4023","BK4585"],"gpt_icon":0},{"id":"2525416818","title":"PagerDuty Named a Leader and Outperformer in GigaOm Radar for IT Incident Response Platforms for Third Consecutive Year","url":"https://stock-news.laohu8.com/highlight/detail?id=2525416818","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2525416818?lang=en_us&edition=fundamental","pubTime":"2025-04-08 21:00","pubTimestamp":1744117200,"startTime":"0","endTime":"0","summary":"PagerDuty has been named a Leader and an Outperformer in the 2025 GigaOm Radar for IT Incident Response Platforms.GigaOm report recognizes the PagerDuty Operations Cloud with top three scores in all categories showcasing strengths in incident response management, real-time mobile support and comprehensive AIOps capabilities. Read the full GigaOm Radar for IT Incident Response Platforms and learn more about the PagerDuty Operations Cloud here.PagerDuty ranked among the top three companies in the areas that GigaOm considers differentiating and critical in the sector, including:. Key Features that differentiate solutions, highlighting the primary criteria to be considered when evaluating an IT incident response platform solution. PagerDuty had the highest score of 4.4 out of 5.In a market shaped by rising complexity and the need for operational resilience, GigaOm highlighted numerous strengths of the PagerDuty Operations Cloud, including advanced incident response capabilities, seamless m","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":["rate"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/pagerduty-named-leader-outperformer-gigaom-130000100.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":["PD"],"gpt_icon":0},{"id":"2525041676","title":"Verizon Frontline provides critical Unmanned Aircraft Systems support for New Orleans PD during Mardi Gras","url":"https://stock-news.laohu8.com/highlight/detail?id=2525041676","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2525041676?lang=en_us&edition=fundamental","pubTime":"2025-04-07 22:00","pubTimestamp":1744034400,"startTime":"0","endTime":"0","summary":"What you need to know: The Verizon Frontline Crisis Response Team supported the New Orleans Police Department (NOPD) with Unmanned Aircraft Systems (UAS) support during the busiest week of Mardi Gras.","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/2025/04/07/3056892/0/en/Verizon-Frontline-provides-critical-Unmanned-Aircraft-Systems-support-for-New-Orleans-PD-during-Mardi-Gras.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":null,"symbols":["IE00BSNM7G36.USD","LU0225284248.USD","LU1169590202.USD","LU1585245621.USD","LU0225771236.USD","LU0868494708.USD","BK4588","LU1066051811.HKD","LU1066051498.USD","BK4534","LU1621767737.EUR","LU0306807586.USD","LU0942090050.USD","BK4515","LU1621768206.USD","LU1571399168.USD","LU1066051225.USD","BK4023","LU1914381329.SGD","LU0321505439.SGD","LU1066053197.SGD","PD","BK4533","LU0321505868.SGD","LU0868494617.USD","LU0306806265.USD","LU0985481810.HKD","VZ","BK4115","LU0098860793.USD","LU1169589451.USD","LU0320765646.SGD","BK4585","LU2384288077.EUR","BK4581","BK4559","LU1162221912.USD","LU1059921491.USD","LU1621768115.EUR","LU1621767810.EUR","LU1366192091.USD","LU1699723380.USD","BK4550","LU1430594728.SGD"],"gpt_icon":0},{"id":"2525501799","title":"NKGen Biotech Presents Data from Phase 1/2a Clinical Trial of Troculeucel in Moderate Alzheimer’s Disease at the International Conference on Alzheimer’s and Parkinson’s Diseases (AD/PD™ 2025)","url":"https://stock-news.laohu8.com/highlight/detail?id=2525501799","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2525501799?lang=en_us&edition=fundamental","pubTime":"2025-04-07 20:05","pubTimestamp":1744027500,"startTime":"0","endTime":"0","summary":"Moderate Alzheimer’s disease (AD) patients in the trial received the highest dose of troculeucel to date at 6 billion cells per treatment. After 12 months of treatment, both patients who completed 17 ","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/2025/04/07/3056692/0/en/NKGen-Biotech-Presents-Data-from-Phase-1-2a-Clinical-Trial-of-Troculeucel-in-Moderate-Alzheimer-s-Disease-at-the-International-Conference-on-Alzheimer-s-and-Parkinson-s-Diseases-AD.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":["LU1169590202.USD","BK4023","PD","LU1169589451.USD"],"gpt_icon":0},{"id":"2525301085","title":"Amneal Announces New Data from Phase 3 Study Showing Significant Improvements in Sleep Quality with CREXONT® (Carbidopa and Levodopa) Extended-Release Capsules in Parkinson’s Disease","url":"https://stock-news.laohu8.com/highlight/detail?id=2525301085","media":"Business Wire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2525301085?lang=en_us&edition=fundamental","pubTime":"2025-04-07 20:00","pubTimestamp":1744027200,"startTime":"0","endTime":"0","summary":"- Analysis of RISE-PD presented at AAN 2025 showed CREXONT treatment significantly improved patients’ Parkinson’s Disease Sleep Scale-2  total and sub-scale scores. - Treatment with CREXONT also resulted in significantly more patients waking up in an \"On\" state compared to immediate-release CD/LD patients, as part of separate study analysis. BRIDGEWATER, N.J., April 07, 2025----Amneal Pharmaceuticals, Inc.  , a global biopharmaceutical company, today announced a new analysis of the pivotal RISE-PD Phase 3 study showed that patients who successfully converted to CREXONT from immediate release  carbidopa/levodopa  experienced statistically significant improvements in sleep quality. These improvements were measured by their Parkinson’s Disease Sleep Scale-2  total scores, showing a mean difference of -2.35 .A separate analysis of Hauser diary entries, which is a commonly used PD symptom tracking tool, from patients who completed the RISE-PD study will also be presented at AAN. Treatment w","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/amneal-announces-data-phase-3-120000084.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":["CD","BK4161","AAN","CNS","LU0256863902.USD","LU0124384867.USD","BK4585","AMRX","LU0417517546.SGD","LU1169590202.USD","LU1169589451.USD","LU0256863811.USD","BK4023","IR","LU1978683503.SGD","BK4178","SG9999001440.SGD","BK4116","BK4007","BK4135","BK4588","PD"],"gpt_icon":0},{"id":"2525045971","title":"Tharimmune Announces Positive Data with Novel Biparatopic PD-1/VEGF and Multispecific HER2/HER3 Biologics Leveraging Proprietary EpiClick(TM) Technology","url":"https://stock-news.laohu8.com/highlight/detail?id=2525045971","media":"ACCESS Newswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2525045971?lang=en_us&edition=fundamental","pubTime":"2025-04-07 20:00","pubTimestamp":1744027200,"startTime":"0","endTime":"0","summary":"BRIDGEWATER, NJ / ACCESS Newswire / April 7, 2025 / Tharimmune, Inc.  , a clinical-stage biotechnology company focused on immunology and inflammation, today announced preclinical data from its expanded pipeline with HS1940, a dual-target multispecific biologic engineered to bind to both Programmed Death-1  and Vascular Endothelial Growth Factor , and HS3215, a dual-target biologic binding to Human Epidermal Growth Factors 2  and 3  receptors. Using its proprietary EpiClick Technology, a versatile multispecific antibody engineering platform, HS1940 and HS3215 represent a key expansion of Tharimmune's product pipeline and underscores the Company's commitment to addressing unmet needs.HS1940 is designed as a biparatopic  biologic, simultaneously engaging the PD-1 pathway and inhibiting angiogenesis. By using multiple, previously undruggable epitopes on PD-1, and blocking VEGF-mediated tumor vascularization, HS1940 may broaden treatment options and improve outcomes across multiple types 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