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CytomX Therapeutics

2.64

+0.240010.00%

Post-market: 2.650.0100+0.38%18:59 EDT

Volume:3.41M

Turnover:8.89M

Market Cap:415.92M

PE:5.44

High:2.71

Open:2.46

Low:2.43

Close:2.40

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Overview Company News Filings

CytomX Therapeutics Inc expected to post earnings of 12 cents a share - Earnings Preview

Moderna Inc. Publishes Document on mRNA-Encoded Masked IL-12 for Improved Systemic Tolerability and Anti-Tumor Efficacy

Piper Sandler Reaffirms Their Buy Rating on CytomX Therapeutics (CTMX)

BRIEF-Cytomx Therapeutics Presents Preclinical Data For mRNA Encoded Masked Il-12 Molecule In Collaboration With Moderna

CytomX Therapeutics Presents Preclinical Data for Mrna Encoded Masked Il-12 Molecule in Collaboration With Moderna at Aacr Annual Meeting

THOMSON REUTERS

CytomX Therapeutics Presents Preclinical Data for mRNA Encoded Masked IL-12 Molecule in Collaboration with Moderna at AACR Annual Meeting

CytomX Gears Up to Report Q1 Earnings: Here's What to Expect

SRPT Provides Pipeline Updates on Rare Muscular Disorder Therapies

CytomX Therapeutics Is Maintained at Overweight by Piper Sandler

FDA Grants Three Fast Track Tags to Allogene's Autoimmune Disease Drug

SRPT Stock Down After EMA Places Clinical Hold on DMD Gene Therapy

BMRN's PKU Drug Palynziq Meets Goal in Late-Stage Pediatric Study

CORT Shares Rise as Relacorilant Combo Meets Ovarian Cancer Study Goal

CytomX Therapeutics participates in a conference call with JPMorgan

FDA Accepts Merck's Filing for Subcutaneous Version of Keytruda

FDA Accepts Sanofi's Filing for Multiple Sclerosis Drug Tolebrutinib

Elevation Oncology Plunges 42% on Ending Development of Lead Drug

Akebia Stock Drops 28% on Pricing of $50M Common Stock Offering

Top Executives Cash Out: CytomX Therapeutics Stock Transactions Unveiled!

SRPT Nosedives 27% on Patient Death Following DMD Therapy Infusion

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Publishes Document on mRNA-Encoded Masked IL-12 for Improved Systemic Tolerability and Anti-Tumor Efficacy","url":"https://stock-news.laohu8.com/highlight/detail?id=2531482017","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2531482017?lang=en_us&edition=fundamental","pubTime":"2025-04-30 07:20","pubTimestamp":1745968815,"startTime":"0","endTime":"0","summary":"Moderna Inc. has published a document detailing a study on mRNA-encoded masked IL-12, showcasing its potential as a safe and effective immunotherapy. The study highlights the approach of using CytomX's PROBODY Therapeutics masking technology alongside Moderna's mRNA platform to improve systemic tolerability and maintain anti-tumor efficacy in preclinical models. The full document can be accessed through the link below.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Moderna Inc. published the original content used to generate this news brief on April 28, 2025, and is solely responsible for the information contained therein.","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250429:nNDL6T0zLc:1","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":["BK4532","BK4551","BK4585","BK4568","BK4501","BK4534","BK4588","BK4548","MRNA","CTMX","BK4533","BK4139"],"gpt_icon":0},{"id":"2531788137","title":"Piper Sandler Reaffirms Their Buy Rating on CytomX Therapeutics (CTMX)","url":"https://stock-news.laohu8.com/highlight/detail?id=2531788137","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2531788137?lang=en_us&edition=fundamental","pubTime":"2025-04-29 18:39","pubTimestamp":1745923193,"startTime":"0","endTime":"0","summary":"Piper Sandler analyst Edward Tenthoff reiterated a Buy rating on CytomX Therapeutics (CTMX – Research Report) today and set a price target of $2.50...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/piper-sandler-reaffirms-their-buy-rating-on-cytomx-therapeutics-ctmx-2?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":["rate"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/blurbs/piper-sandler-reaffirms-their-buy-rating-on-cytomx-therapeutics-ctmx-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":["CTMX"],"gpt_icon":0},{"id":"2531264753","title":"BRIEF-Cytomx Therapeutics Presents Preclinical Data For mRNA Encoded Masked Il-12 Molecule In Collaboration With Moderna","url":"https://stock-news.laohu8.com/highlight/detail?id=2531264753","media":"Reuters","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2531264753?lang=en_us&edition=fundamental","pubTime":"2025-04-29 05:25","pubTimestamp":1745875554,"startTime":"0","endTime":"0","summary":"BRIEF-Cytomx Therapeutics Presents Preclinical Data For mRNA Encoded Masked Il-12 Molecule In Collaboration With Moderna April 28 (Reuters) - CytomX Therapeutics Inc CTMX.O:CYTOMX THERAPEUTICS PRESENT","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250428:nTUAB0RR7V:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CTMX","BK4139"],"gpt_icon":0},{"id":"2531250644","title":"CytomX Therapeutics Presents Preclinical Data for Mrna Encoded Masked Il-12 Molecule in Collaboration With Moderna at Aacr Annual Meeting","url":"https://stock-news.laohu8.com/highlight/detail?id=2531250644","media":"THOMSON REUTERS","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2531250644?lang=en_us&edition=fundamental","pubTime":"2025-04-29 04:00","pubTimestamp":1745870401,"startTime":"0","endTime":"0","summary":null,"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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250428:nTUAB0RR7V:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"reuters_en_live","symbols":["BK4139","CTMX"],"gpt_icon":0},{"id":"2531125091","title":"CytomX Therapeutics Presents Preclinical Data for mRNA Encoded Masked IL-12 Molecule in Collaboration with Moderna at AACR Annual Meeting","url":"https://stock-news.laohu8.com/highlight/detail?id=2531125091","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2531125091?lang=en_us&edition=fundamental","pubTime":"2025-04-29 04:00","pubTimestamp":1745870400,"startTime":"0","endTime":"0","summary":"Novel engineering approach to developing an mRNA-encoded masked IL-12 therapeutic demonstrates potent anti-tumor activity with significantly enhanced tolerability. AboutCytomX Therapeutics, Inc.CytomX is a clinical-stage, oncology-focused biopharmaceutical company focused on developing novel conditionally activated, masked biologics designed to be localized to the tumor microenvironment. By pioneering a novel pipeline of localized biologics, powered by its PROBODYtherapeutic platform, CytomX’s vision is to create safer, more effective therapies for the treatment of cancer. CytomX’s robust and differentiated pipeline comprises therapeutic candidates across multiple treatment modalities including antibody-drug conjugates , T-cell engagers, and immune modulators such as cytokines. CytomX’s clinical-stage pipeline includes CX-2051 and CX-801. CX-2051 is a masked, conditionally activated ADC directed toward epithelial cell adhesion molecule , armed with a topoisomerase-1 inhibitor payload. ","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/cytomx-therapeutics-presents-preclinical-data-200000860.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":["BK4509","BK4548","BK4108","LU0359201612.USD","IE00BYQNZ168.SGD","BK4563","SG9999011746.SGD","CTMX","IE00B12V2V27.USD","BK4535","BK4139","BK4565","LU1023057109.AUD","BK4552","BK4571","LU0359202008.SGD","LU2039709279.SGD","BK4526","BK4531","01698","TME","IE00BYTNYN87.SGD"],"gpt_icon":0},{"id":"2530558163","title":"CytomX Gears Up to Report Q1 Earnings: Here's What to Expect","url":"https://stock-news.laohu8.com/highlight/detail?id=2530558163","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530558163?lang=en_us&edition=fundamental","pubTime":"2025-04-25 22:14","pubTimestamp":1745590440,"startTime":"0","endTime":"0","summary":"CytomX TherapeuticsCTMX, a clinical-stage oncology company, is expected to beat first-quarter 2025 earnings when it reports quarterly results soon. . The Zacks Consensus Estimate for CTMX’s earnings per share in the to-be-reported quarter is currently pegged at 18 cents. CytomX recognizes collaboration revenues from its ongoing partnership agreements with several biotech companies like Amgen AMGN, Astellas,Bristol Myers, Moderna, AbbVie and Regeneron. The Zacks Consensus Estimate for revenues is pinned at $35.52 million.Let's see how things have shaped up for the upcoming quarterly release.In January 2025, CytomX announced its investigational candidate, CX-2051 ,as its lead program. The candidate is initially being developed for advanced metastatic colorectal cancer  in a phase I dose-escalation study, which is currently enrolling patients.In January 2025, CytomX also announced plans to reduce its workforce by about 40% to prioritize clinical programs and enhance financial flexibility.","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":["earning"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/cytomx-gears-report-q1-earnings-141400145.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":["CTMX"],"gpt_icon":0},{"id":"2527217592","title":"SRPT Provides Pipeline Updates on Rare Muscular Disorder Therapies","url":"https://stock-news.laohu8.com/highlight/detail?id=2527217592","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527217592?lang=en_us&edition=fundamental","pubTime":"2025-04-16 19:32","pubTimestamp":1744803120,"startTime":"0","endTime":"0","summary":"Sarepta Therapeutics SRPT announced updates from its clinical programs, which focus on targeting different subtypes of limb-girdle muscular dystrophy , a group of rare genetic disorders marked by progressive muscle weakness.Following positive FDA feedback, the company is advancing a fourth LGMD program to clinical development. Sarepta will soon start screening and dosing patients in the first-in-human clinical SRP-9005-101  study, to evaluate its investigational gene therapy SRP-9005 for LGMD type 2C/R5 .SRPT also announced completion of enrollment and dosing in the phase I proof-of-concept SRP-9004-102  study, which is evaluating SRP-9004 in patients with LGMD type 2D/R3 .The company also reiterated its plans to report data from the late-stage EMERGENE study, evaluating SRP-9003 in patients with LGMD type 2E/R4 , by first-half 2025. This study’s primary endpoint is the biomarker expression of the beta-sarcoglycan protein, whose absence is the sole cause of the disease. Following a pre","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/srpt-provides-pipeline-updates-rare-113200363.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":["IE0009355771.USD","IE00BJJMRZ35.SGD","BK4139","SRPT","IE00B2B36J28.USD","LU1559883803.SGD","CTMX","IE0002141913.USD","IE00BJT1NW94.SGD","BK4585","BK4007","LU0566484027.USD","ANIP","03165","IE00BFTCPJ56.SGD","RHHBY"],"gpt_icon":0},{"id":"2527196931","title":"CytomX Therapeutics Is Maintained at Overweight by Piper Sandler","url":"https://stock-news.laohu8.com/highlight/detail?id=2527196931","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527196931?lang=en_us&edition=fundamental","pubTime":"2025-04-14 22:59","pubTimestamp":1744642740,"startTime":"0","endTime":"0","summary":"Ratings actions from Benzinga: https://www.benzinga.com/quote/CTMX/analyst-ratings \n\n\n \n\n\n  (END) Dow Jones Newswires\n\n\n  April 14, 2025 10:59 ET (14:59 GMT)","market":"sg","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://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":["CTMX"],"gpt_icon":0},{"id":"2525318890","title":"FDA Grants Three Fast Track Tags to Allogene's Autoimmune Disease Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2525318890","media":"Zacks","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2525318890?lang=en_us&edition=fundamental","pubTime":"2025-04-08 18:46","pubTimestamp":1744109160,"startTime":"0","endTime":"0","summary":"Allogene Therapeutics ALLO announced that the FDA has granted three fast track designations to its investigational CRISPR-based allogeneic CAR-T therapy, ALLO-329.These designations apply to three autoimmune diseases — systemic lupus erythematosus , idiopathic inflammatory myopathy  and diffuse systemic sclerosis .How Does the Fast Track Tag Benefit ALLO’s Drug Development?Fast track designation is designed to facilitate the development and expedite the review of drugs that treat serious conditions, meet an unmet medical need, or offer a potential advantage over existing treatments. Per the FDA, the purpose of granting this designation is to ‘get important new drugs to the patient earlier.’。In the past 60 days, estimates for CytomX Therapeutics’ 2025 EPS have improved from a loss of 31 cents to a profit of 25 cents. During the same timeframe, estimates for loss per share for 2026 have","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/fda-grants-three-fast-track-104600523.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":["BK4567","ETNB","IE00BYQQ9H92.USD","IE00BFXG0V08.USD","CTMX","FAST","ANIP","BK4104","BK4139","BK4007","BK4505","BK4585","IIM","ALLO","SLE","IE00B5TLWC47.USD","BK4588","BK4077"],"gpt_icon":0},{"id":"2524420475","title":"SRPT Stock Down After EMA Places Clinical Hold on DMD Gene Therapy","url":"https://stock-news.laohu8.com/highlight/detail?id=2524420475","media":"Zacks","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524420475?lang=en_us&edition=fundamental","pubTime":"2025-04-04 19:29","pubTimestamp":1743766140,"startTime":"0","endTime":"0","summary":"Shares of Sarepta Therapeutics SRPT dropped more than 6% yesterday after the EMA placed a clinical hold on all studies evaluating Elevidys, its one-shot gene therapy for Duchenne muscular dystrophy . The therapy has been developed in collaboration with pharma giant Roche RHHBY.This hold has been placed in response to a patient’s death post-treatment with Elevidys, which was reported last month. Though the death was due to acute liver failure , Sarepta believes that the patient’s recent CMV infection might have contributed to the outcome. Investigation is still ongoing.In a letter to the World Duchenne Organization, Roche mentioned that the companies are pausing enrollment and dosing of study participants in three studies evaluating the therapy at the EU study sites. This hold will remain ‘until the analysis into the cause of death is complete.’。SRPT and RHHBY entered into a licensing agreement in 2019 to develop Elevidys. Per the agreement, Sarepta retains the rights to market the gene","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/srpt-stock-down-ema-places-112900759.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["RHHBY","BK4585","IE0002141913.USD","ANIP","IE00BJJMRZ35.SGD","IE00BFTCPJ56.SGD","IE00BJT1NW94.SGD","SRPT","IE00B2B36J28.USD","CTMX","BK4007","BK4139","03165","IE0009355771.USD"],"gpt_icon":0},{"id":"2524260088","title":"BMRN's PKU Drug Palynziq Meets Goal in Late-Stage Pediatric Study","url":"https://stock-news.laohu8.com/highlight/detail?id=2524260088","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524260088?lang=en_us&edition=fundamental","pubTime":"2025-04-03 22:14","pubTimestamp":1743689640,"startTime":"0","endTime":"0","summary":"BioMarin BMRN has announced positive results from the phase III PEGASUS study evaluating Palynziq  in adolescents aged 12-17 years with phenylketonuria .The study achieved its primary endpoint – patients treated with Palynziq achieved a statistically significant lowering in blood phenylalanine  levels compared to diet alone. The safety results were also consistent with the known profile of the drug.Palynziq is already approved in the United States to reduce blood Phe concentration in adults aged 18 years and older with PKU. The drug is currently the only enzyme therapy to treat the disease in this age group.PKU is a rare genetic disorder that prevents the body from breaking down Phe, an amino acid found in protein-rich foods, leading to toxic levels that can cause severe neurological damage. While newborn screening enables early diagnosis, lifelong dietary management is challenging, creating demand for innovative treatments like those developed by BioMarin.In the past 60 days, estimate","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/bmrns-pku-drug-palynziq-meets-141400981.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":["CTMX","IE00B19Z3B42.SGD","SSI","IE00B19Z3581.USD","IE00B7SZLL34.SGD","IE0002270589.USD","ANIP","BK4566","ETNB","BK4139","BMRN","BK4585","BK4007"],"gpt_icon":0},{"id":"2524128774","title":"CORT Shares Rise as Relacorilant Combo Meets Ovarian Cancer Study Goal","url":"https://stock-news.laohu8.com/highlight/detail?id=2524128774","media":"Zacks","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524128774?lang=en_us&edition=fundamental","pubTime":"2025-04-01 22:50","pubTimestamp":1743519000,"startTime":"0","endTime":"0","summary":"Shares of Corcept Therapeutics Incorporated CORT were up a staggering 109.1% on March 31 after the company announced data from the phase III ROSELLA study, which evaluated its pipeline candidate, relacorilant, in combination with nab-paclitaxel for treating patients with platinum-resistant ovarian cancer.The ROSELLA study met its primary endpoint of improved progression-free survival, as assessed by blinded independent central review .Per management, data from the ROSELLA study suggested that the combo of relacorilant plus nab-paclitaxel has the potential to become a new standard of care for patients with platinum-resistant ovarian cancer.Year to date, shares of Corcept have skyrocketed 126.7% against the industry’s decline of 1.9%.The phase III ROSELLA study evaluated relacorilant in combination with nab-paclitaxel for treating patients with recurrent, platinum-resistant ovarian cancer.Data from the same showed that treatment with relacorilant plus nab-paclitaxel reduced the risk of d","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/cort-shares-rise-relacorilant-combo-145000011.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":["LU2065171402.SGD","ANIP","BK4139","BK4097","CTMX","LU2065171311.SGD","LU2065169927.USD","LU2065170008.USD","BK4007","LU1559883803.SGD","FOLD","BK4532","LU0566484027.USD","OS","CORT"],"gpt_icon":0},{"id":"2524228059","title":"CytomX Therapeutics participates in a conference call with JPMorgan","url":"https://stock-news.laohu8.com/highlight/detail?id=2524228059","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524228059?lang=en_us&edition=fundamental","pubTime":"2025-03-31 23:50","pubTimestamp":1743436214,"startTime":"0","endTime":"0","summary":"Conference call with address top 10 questions in management on March 31 at 12 pm hosted by PMorgan. Webcast Link Published first on TheFly – the ul...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/cytomx-therapeutics-participates-in-a-conference-call-with-jpmorgan-3?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/the-fly/cytomx-therapeutics-participates-in-a-conference-call-with-jpmorgan-3?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["LU2430703251.USD","LU1064131342.USD","LU1668664300.SGD","LU2106854487.HKD","LU0964807845.USD","LU2264538146.SGD","IE00BBT3K403.USD","LU1720051108.HKD","IE00BJLML261.HKD","LU0211331839.USD","LU2357305700.SGD","IE00BWXC8680.SGD","SG9999002224.SGD","LU0496365809.HKD","LU2237443549.SGD","BK4588","IE00BKDWB100.SGD","BK4207","LU2237443895.HKD","LU0149725797.USD","IE00BKVL7J92.USD","LU1162221912.USD","LU0820562030.AUD","LU1145028129.USD","BK4534","BK4504","LU1894683264.USD","BK4566","LU0320765489.SGD","LU0203345920.USD","LU2023250504.SGD","LU1720051017.SGD","LU0211328371.USD","CTMX","LU1366192091.USD","LU2552382058.USD","LU2552382215.SGD","LU1551013425.SGD","IE00BDRTCR15.USD","LU0211326839.USD","LU1629891620.HKD","LU2242649171.HKD","LU0170899867.USD","LU1244550221.USD","IE000M9KFDE8.USD","LU2237443465.HKD","IE00B775SV38.USD","BK4550","LU0215105999.USD"],"gpt_icon":0},{"id":"2523685649","title":"FDA Accepts Merck's Filing for Subcutaneous Version of Keytruda","url":"https://stock-news.laohu8.com/highlight/detail?id=2523685649","media":"Zacks","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2523685649?lang=en_us&edition=fundamental","pubTime":"2025-03-28 23:20","pubTimestamp":1743175200,"startTime":"0","endTime":"0","summary":"Merck MRK announced that the FDA has accepted its regulatory filing seeking approval for the subcutaneous  formulation of the blockbuster drug Keytruda .This filing seeks the agency’s nod for the SC version across all solid tumor indications for which the drug’s intravenous  version is already approved.A final decision is expected by Sept. 23, 2025.The regulatory filing is supported by data from the pivotal phase III 3475A-D77 study that evaluated Keytruda SC against the IV version  for the first-line treatment of adult patients with metastatic non-small cell lung cancer. As announced by Merck in November, the study achieved its primary endpoints, showing that the treatment with the SC version of the drug was at least as effective as the IV version.An approval of the SC version also benefits both patients and physicians. Delivering a drug SC instead of IV can significantly reduce administrat","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/fda-accepts-mercks-filing-subcutaneous-152000184.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":["LU2023250843.SGD","SG9999002224.SGD","LU0208291251.USD","LU1037948897.HKD","BK4516","LU1066051811.HKD","SG9999015358.SGD","SG9999015341.SGD","LU1934455863.HKD","LU2112291526.USD","LU1585245621.USD","LU0965509010.AUD","LU1989772840.SGD","LU0070302665.USD","SG9999001176.SGD","LU0965509283.SGD","LU1116320737.USD","LU1989772923.USD","IE00B4R5TH58.HKD","IE00BJJMRZ35.SGD","LU0289739699.SGD","LU1066053197.SGD","CTMX","BK4550","LU0320765489.SGD","LU1983299246.USD","BK4585","MRK","IE00BSNM7G36.USD","LU1023059063.AUD","ANIP","LU1037948541.HKD","LU1941712264.USD","LU0320765646.SGD","LU1066051498.USD","IE0002141913.USD","BK4139","IE00BLSP4239.USD","IE00BN8TJ469.HKD","LU0861579265.USD","LU0266013472.USD","LU1093756325.SGD","LU0985320562.USD","LU2361044865.SGD","ETNB","IE00BJT1NW94.SGD","SG9999014575.USD","LU0058720904.USD","IE000M9KFDE8.USD"],"gpt_icon":0},{"id":"2522079582","title":"FDA Accepts Sanofi's Filing for Multiple Sclerosis Drug Tolebrutinib","url":"https://stock-news.laohu8.com/highlight/detail?id=2522079582","media":"Zacks","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2522079582?lang=en_us&edition=fundamental","pubTime":"2025-03-25 19:56","pubTimestamp":1742903760,"startTime":"0","endTime":"0","summary":"Sanofi SNY announced that the FDA has accepted its regulatory filing seeking approval for its investigational BTK inhibitor tolebrutinib to treat non-relapsing secondary progressive multiple sclerosis  and slow disability accumulation independent of relapse activity in adults.The filing has been granted priority review by the FDA, bringing down the review period by four months. A final decision is expected by Sept. 28, 2025.The FDA filing is supported by data from three late-stage studies — one  in nrSPMS and two  in relapsing MS . Data from these studies showed that patients treated with tolebrutinib delayed the time to onset of six-month confirmed disability progression when compared to placebo. A similar regulatory filing for the drug is currently under review by the EMA, which is also supported by data from these studies.Per Sanofi, the above results make tolebrutinib the first and the only brain-penetrant BTK inhibitor to treat both the above MS indications. If approved, tolebruti","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/fda-accepts-sanofis-filing-multiple-115600487.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":["LU0098860793.USD","LU2357305700.SGD","LU0971096721.USD","LU2089283258.USD","MG","LU1363072403.SGD","BK4139","LU0158827781.USD","BK4534","LU1668664300.SGD","LU1548497426.USD","LU1720051017.SGD","IE00B19Z4B17.USD","LU0106261372.USD","LU0912757837.SGD","LU1989772840.SGD","IE0031619046.USD","LU2023251221.USD","LU0225283273.USD","IE00BZ1G4Q59.USD","CTMX","LU0106831901.USD","SNY","LU1162221912.USD","IE00B66KJ199.SGD","BK4516","LU1732799900.SGD","SNYNF","IE00BFXG1179.USD","IE00BKVL7J92.USD","BK4588","BK4585","LU1732800096.USD","ANIP","BK4581","LU0314104364.USD","LU0267386448.USD","LU2271345857.HKD","BK4504","LU0795875169.SGD","LU0158827948.USD","ETNB","LU1074936037.SGD","LU2111349929.HKD","LU0320765646.SGD","LU1720051108.HKD","LU2133065610.SGD","BK4123","LU2028103732.USD"],"gpt_icon":0},{"id":"2521940256","title":"Elevation Oncology Plunges 42% on Ending Development of Lead Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2521940256","media":"Zacks","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2521940256?lang=en_us&edition=fundamental","pubTime":"2025-03-22 01:03","pubTimestamp":1742576580,"startTime":"0","endTime":"0","summary":"Shares of Elevation Oncology ELEV plunged more than 40% yesterday after reporting disappointing data from a phase I study on its lead pipeline drug EO-3021 for treating advanced, unresectable or metastatic gastric and gastroesophageal junction  cancers.Data from the study showed that patients who were treated with ELEV’s lead drug showed an objective response rate  of 22.2% —out of 36 evaluable patients, there was one complete response and seven partial responses.Following the disappointing study results, Elevation Oncology decided not to pursue further clinical development of EO-3021. Instead, the company will now shift its focus to solid tumor candidate EO-1022, for which an investigational new drug  filing with the FDA is expected next year. As a result of this decision, ELEV is now without a pipeline candidate in clinical development. These factors were likely responsible for the significant drop in share price.In the past 60 days, estimates for CytomX Therapeutics’ 2025 EPS have i","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/elevation-oncology-plunges-42-ending-170300990.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":["BK4007","ELEV","CTMX","ETNB","ANIP","BK4539","BK4139","ORR","BK4585"],"gpt_icon":0},{"id":"2521946256","title":"Akebia Stock Drops 28% on Pricing of $50M Common Stock Offering","url":"https://stock-news.laohu8.com/highlight/detail?id=2521946256","media":"Zacks","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2521946256?lang=en_us&edition=fundamental","pubTime":"2025-03-22 01:01","pubTimestamp":1742576460,"startTime":"0","endTime":"0","summary":"Akebia Therapeutics AKBA recently announced that it is floating a secondary issue of 25 million shares of its common stock to the public at an issue price of $2 per share, amounting to $50 million.The company also granted an option to underwriters of the issue to purchase an additional 3.75 million shares at the same price.The secondary offering is expected to close today.Akebia’s shares fell more than 28% yesterday after the announcement. Though the issue does not significantly dilute the existing shareholder base, the issue price per share did not sit well with investors. The issue price was at a discount to the closing price on Thursday, with the stock closing at $2.04.Year to date, shares of Akebia have outperformed the industry.Akebia plans to use the net proceeds from this new issue and its existing cash balance to fund working capital and general corporate purposes, which may include supporting research, development and commercial activities for its marketed and pipeline drugs.A","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/akebia-stock-drops-28-pricing-170100693.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["ETNB","BK4139","CTMX","BK4007","ANIP","BK4585","AKBA"],"gpt_icon":0},{"id":"2521844926","title":"Top Executives Cash Out: CytomX Therapeutics Stock Transactions Unveiled!","url":"https://stock-news.laohu8.com/highlight/detail?id=2521844926","media":"TIPRANKS","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2521844926?lang=en_us&edition=fundamental","pubTime":"2025-03-21 10:04","pubTimestamp":1742522673,"startTime":"0","endTime":"0","summary":"New insider activity at CytomX Therapeutics ( ($CTMX) ) has taken place on March 21, 2025. In recent transactions involving CytomX Therapeutics sto...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/insider-trading/top-executives-cash-out-cytomx-therapeutics-stock-transactions-unveiled?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/insider-trading/top-executives-cash-out-cytomx-therapeutics-stock-transactions-unveiled?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["BK4139","CTMX"],"gpt_icon":0},{"id":"2520160326","title":"SRPT Nosedives 27% on Patient Death Following DMD Therapy Infusion","url":"https://stock-news.laohu8.com/highlight/detail?id=2520160326","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520160326?lang=en_us&edition=fundamental","pubTime":"2025-03-20 01:38","pubTimestamp":1742405880,"startTime":"0","endTime":"0","summary":"Per the company, this patient died of acute liver failure. While acute liver injury is a known risk of Elevidys, this is the first time a death has been reported of anyone taking the therapy. However, Sarepta stated that the patient also had a recent CMV infection, which may have contributed to the outcome, as CMV can damage the liver.Sarepta has reported the event to health authorities, clinical study investigators and prescribing physicians. It intends to update Elevidys’ prescribing information accordingly. Despite the incident, the company maintains that the benefit-risk profile of its gene therapy remains positive, with over 800 patients treated in clinical studies or commercial 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