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CytomX Therapeutics

0.5800

-0.0558-8.78%

Post-market: 0.58000.00000.00%16:06 EDT

Volume:915.62K

Turnover:557.53K

Market Cap:46.46M

PE:1.54

High:0.6500

Open:0.6500

Low:0.5800

Close:0.6358

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Overview Company News Filings

CytomX Therapeutics Inc -Revised Focus and Associated Cost and Headcount Reductions Expected to Extend Cash Runway Into Q2 of 2026

THOMSON REUTERS

KOD Stock Rallies 271% in 6 Months on Eye Disease Program Updates

Here's Why Arcutis Stock More Than Doubled in Market Value in One Year

MESO Stock Surges 80% in a Month After FDA Approval of GVHD Drug

CAPR Stock Up on Completion of Rolling Submission of DMD Drug BLA

Neumora Stock Hits Record Low on Depression Drug Study Failure

PGEN Stock Surges More Than 40% in a Week: What's Driving the Rally?

VSTM Up as NDA for Ovarian Cancer Combo Gets FDA's Priority Review Tag

CytomX heading into ‘major catalyst year,’ says JonesResearch

JNJ Inks Licensing Deal With Kaken for Eczema Candidate KP-723

Vertex Secures FDA Approval for New Cystic Fibrosis Drug Alyftrek

AZN's Tagrisso Gets Approval in the EU for Expanded Use in NSCLC

VRTX Down as Non-Opioid Drug Shows Similar Pain Reduction as Placebo

KRYS Reports Upbeat Initial Data From Lung Cancer Study of KB707

SRPT Finishes Enrolment in Late-Stage Study for Rare Muscular Disorder

GILD's Trodelvy Gets Second Breakthrough Therapy Tag for Lung Cancer

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It is a novel anti-VEGF antibody biopolymer conjugate, which is being evaluated for treating retinal vascular diseases.In late 2023, Kodiak rebooted the development program of tarcocimab following positive phase III results from the GLOW1 study, which evaluated the treatment in patients with moderately severe to severe non-proliferative diabetic retinopathy. Leveraging the GLOW1 study's success, Kodiak initiated the GLOW2 study in late 2023 to further investigate tarcocimab for diabetic retinopathy  and began dosing patients in May 2024, with enrollment expected to be completed soon. 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CAPR’s lead product candidate and only clinical pipeline asset, deramiocel, is an investigational, allogeneic cardiac-derived cell therapy. A final decision of the FDA is anticipated in the second half of 2024.Capricor initiated its rolling submission process for the deramiocel BLA in October 2024, based on a successful pre-BLA meeting with the FDA. The completion of the submission process has also triggered a $10 million milestone payment from its distribution partner, Nippon Shinyaku, under the terms of the companies’ U.S. Commercialization and Distribution Agreement. The impending influx of cash is set to strengthen CAPR’s cash position.In the past three months, shares of Capricor have plunged 30.9% compared with the indu","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/capr-stock-completion-rolling-submission-152300104.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":["CSTL","BK4139","CAPR","SPRO","BK4196","CTMX"],"gpt_icon":0},{"id":"2500145917","title":"Neumora Stock Hits Record Low on Depression Drug Study Failure","url":"https://stock-news.laohu8.com/highlight/detail?id=2500145917","media":"Zacks","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2500145917?lang=en_us&edition=fundamental","pubTime":"2025-01-03 22:14","pubTimestamp":1735913640,"startTime":"0","endTime":"0","summary":"The phase III KOASTAL-1 study evaluated the efficacy and safety of navacaprant against placebo in adults with moderate-to-severe MDD over a six-week treatment period. The study failed to achieve its primary endpoint – treatment with the drug failed to demonstrate a significant improvement over placebo in alleviating depression symptoms, as measured by the Montgomery-Asberg Depression Rating Scale .The study also failed to show statistically significant improvement in the reduction of anhedonia , as assessed by the Snaith-Hamilton Pleasure Scale .The KOASTAL-1 study is one of the three late-stage studies in the KOASTAL program evaluating navacaprant in the MDD indication. Despite the study's failure, Neumora intends to continue the other two studies. In the meantime, management continues to further analyze the study results, as management claimed that the drug showed an efficacy signal in female patients.Following the news, shares of Neumora hit an all-time low of $1.83. The latest anno","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/neumora-stock-hits-record-low-141400263.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":["NMRA","SPRO","BK4196","BK4007","ABVC","CTMX","BK4139","CSTL"],"gpt_icon":0},{"id":"2500902522","title":"PGEN Stock Surges More Than 40% in a Week: What's Driving the Rally?","url":"https://stock-news.laohu8.com/highlight/detail?id=2500902522","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2500902522?lang=en_us&edition=fundamental","pubTime":"2025-01-03 02:28","pubTimestamp":1735842480,"startTime":"0","endTime":"0","summary":"Shares of Precigen PGEN have soared nearly 43% in the past week after the company provided an encouraging regulatory update for its lead pipeline program.Last week, Precigen announced that it has completed a rolling submission for a biologic license application  seeking the FDA’s accelerated approval for PRGN-2012, an experimental gene therapy to treat adults with recurrent respiratory papillomatosis .A rare disease, RRP causes benign tumors  to grow in the respiratory tract, most commonly in the larynx . It is caused by two types of human papilloma virus  – HPV 6 and HPV 11.The BLA is supported by data from a pivotal phase I/II study that evaluated PRGN-2012 for the treatment of adult patients with RRP. Data from the study showed that more than 50% of patients achieved a complete response . Also, more than 85% of patients experienced a reduction in surgical interventions in the year after receiving PRGN-2012 compared to the year before receiving the therapy.Precigen currently carries ","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/pgen-stock-surges-more-40-182800609.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":["BK4139","INO","BK4196","CSTL","BK4568","PGEN","BK4583","CTMX"],"gpt_icon":0},{"id":"2500007971","title":"VSTM Up as NDA for Ovarian Cancer Combo Gets FDA's Priority Review Tag","url":"https://stock-news.laohu8.com/highlight/detail?id=2500007971","media":"Zacks","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2500007971?lang=en_us&edition=fundamental","pubTime":"2025-01-02 22:56","pubTimestamp":1735829760,"startTime":"0","endTime":"0","summary":"Both avutometinib and defactinib have been in-licensed by Verastem from other pharmaceutical companies. Avutometinib is an RAF/MEK clamp, while defactinib is a best-in-class selective FAK inhibitor.In the past three months, shares of Verastem have surged 86.6% against the industry’s 9.5% decline.More on the FDA Acceptance of Avutometinib NDA for LGSOC. At present, there are no FDA-approved treatments specifically for LGSOC, a rare and distinct type of ovarian cancer with unique biology and treatment responses compared to high-grade serous ovarian cancer, representing a huge unmet medical need. Per Verastem, an estimated 6,000-8,000 women in theUnited Statesand 80,000 worldwide suffer from this disease. The standard of care treatment includes hormone therapy and chemotherapy.Currently, the company is enrolling patients with recurrent LGSOC regardless of KRAS mutation status in the global phase III RAMP 301 study, which is expected to serve as a confirmatory study for the initial indica","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/vstm-nda-ovarian-cancer-combo-145600394.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":["CSTL","BK4139","BK4196","VSTM","CTMX","SPRO"],"gpt_icon":0},{"id":"2495540747","title":"CytomX heading into ‘major catalyst year,’ says JonesResearch","url":"https://stock-news.laohu8.com/highlight/detail?id=2495540747","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2495540747?lang=en_us&edition=fundamental","pubTime":"2024-12-30 22:15","pubTimestamp":1735568125,"startTime":"0","endTime":"0","summary":"JonesResearch analyst Soumit Roy keeps a Buy rating on CytomX Therapeutics (CTMX) with a $7 price target after the company announced the new drug a...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/cytomx-heading-into-major-catalyst-year-says-jonesresearch?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-heading-into-major-catalyst-year-says-jonesresearch?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":["BK4139","CTMX"],"gpt_icon":0},{"id":"2494385582","title":"JNJ Inks Licensing Deal With Kaken for Eczema Candidate KP-723","url":"https://stock-news.laohu8.com/highlight/detail?id=2494385582","media":"Zacks","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2494385582?lang=en_us&edition=fundamental","pubTime":"2024-12-27 20:17","pubTimestamp":1735301820,"startTime":"0","endTime":"0","summary":"How the Licensing Deal for the AD Program Benefits JNJ. The licensing deal with Kaken reinforces Johnson & Johnson’s dedication to targeting disease-specific pathways across diverse patient populations, leveraging innovative mechanisms and approaches to revolutionize the treatment of AD and other autoimmune and allergic conditions.Per JNJ, most AD patients fail to achieve remission with currently available treatments, representing a huge unmet medical need. The company believes that the STAT6 program stands out as a promising research area, offering the potential for a safe and effective novel oral therapy for those suffering from AD and other autoimmune diseases.In the past three months, shares of JNJ have lost 10.2% compared with the industry’s 13.8% decline.Some better-ranked stocks from the sector areCastle BiosciencesCSTL,CytomX TherapeuticsCTMX andSpero TherapeuticsSPRO, each sporting a Zacks Rank #1  at present. You can seethe complete list of today’s Zacks #1 Rank stocks here.","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/jnj-inks-licensing-deal-kaken-121700393.html","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":"yahoofinance","symbols":["LU1894683348.USD","BK4568","LU1244550494.USD","IE0009355771.USD","IE00BJT1NW94.SGD","LU0289739699.SGD","LU1221951129.SGD","BK4532","LU1261432733.SGD","LU0122379950.USD","IE00B4R5TH58.HKD","LU0345770993.USD","LU0203347892.USD","LU0795875169.SGD","CSTL","LU0889566641.SGD","IE00BFTCPJ56.SGD","LU1674673691.USD","LU0203345920.USD","LU1066051498.USD","JNJ","LU1196500208.SGD","LU1221951046.USD","BK4588","LU0466842654.USD","BK4585","IE00BGHQF631.EUR","LU1674673428.USD","LU0234570918.USD","BK4550","LU1057294990.SGD","IE00BSNM7G36.USD","LU1778281490.HKD","LU0058720904.USD","SG9999002224.SGD","IE000M9KFDE8.USD","CTMX","LU0098860793.USD","LU0912757837.SGD","IE00B3PB1722.GBP","BK4139","BK4581","LU1732799900.SGD","LU1066051811.HKD","IE00BDGV0183.EUR","LU1914381329.SGD","BK4196","LU1066051225.USD","LU1032466523.USD","SPRO"],"gpt_icon":0},{"id":"2493797799","title":"Vertex Secures FDA Approval for New Cystic Fibrosis Drug Alyftrek","url":"https://stock-news.laohu8.com/highlight/detail?id=2493797799","media":"Zacks","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493797799?lang=en_us&edition=fundamental","pubTime":"2024-12-24 02:44","pubTimestamp":1734979440,"startTime":"0","endTime":"0","summary":"Vertex Pharmaceuticals VRTX announced that the FDA has approved its next-in-class vanza triple therapy for treating people with cystic fibrosis  aged six years and above. The drug will be marketed under the brand name Alyftrek.Post the FDA’s approval, the orally administered Alyftrek has been approved for use in CF patients aged six years and older who have at least one F508del mutation or another responsive mutation in the CF transmembrane conductance regulator  gene responsive to the drug. The drug will be available at a wholesale acquisition cost of $370,269 on an annual basis.The FDA’s decision came earlier than the expected PDUFA date of Jan 2, 2025. The approval is based on data from a comprehensive late-stage program, which showed that treatment with once-daily Alyftrek enhanced patient benefit compared to Vertex’s blockbuster CF drug Trikafta , which is required to be administered twice daily. The drug is also eligible for use in CF patients who have discontinued Trikafta or Ve","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/UgiI07ytew_hNcL7MgLFiA--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/5c26ab1f8b890434759145296588998c","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/UgiI07ytew_hNcL7MgLFiA--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/5c26ab1f8b890434759145296588998c"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/vertex-secures-fda-approval-cystic-184400620.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["LU0566484027.USD","LU1069344957.HKD","BK4138","LU1093756168.USD","LU2362541513.USD","LU2237438978.USD","LU2417539215.USD","VRTX","CTMX","BK4548","BK4588","LU0109394709.USD","IE00B2B36J28.USD","LU0058720904.USD","BK4023","LU0320765992.SGD","VERX","BK4196","IE00B19Z3581.USD","VTNR","IE0002141913.USD","LU0417517546.SGD","LU1430594728.SGD","CF","IE00BFTCPJ56.SGD","LU2236285917.USD","BK4567","BK4534","LU0256863811.USD","BK4551","LU0234570918.USD","BK4093","CSTL","BK4585","IE00B19Z3B42.SGD","LU0889565916.HKD","MRNA","BK4139","BK4532","LU2362541273.HKD","LU1585245621.USD","LU1093756325.SGD","LU0061475181.USD","BK4501","IE00B19Z9P08.USD","IE00BZ9MQY76.HKD","LU2456880835.USD","BK4533","IE00B4R5TH58.HKD","LU0079474960.USD"],"gpt_icon":0},{"id":"2493934307","title":"AZN's Tagrisso Gets Approval in the EU for Expanded Use in NSCLC","url":"https://stock-news.laohu8.com/highlight/detail?id=2493934307","media":"Zacks","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493934307?lang=en_us&edition=fundamental","pubTime":"2024-12-23 23:56","pubTimestamp":1734969360,"startTime":"0","endTime":"0","summary":"AstraZenecaAZN announced that its blockbuster cancer drug, Tagrisso , has been approved in the EU for expanded use in non-small cell lung cancer .The eligible patient population includes adults with locally advanced, unresectable NSCLC with EGFR exon 19 deletions  or exon 21  substitution mutations whose disease has not progressed during or following platinum-based chemoradiation therapy. The FDAapprovedthis combinationin September for a similar indication.The nod in the EU is based on data from the phase III LAURAstudy, which showed that treatment with Tagrisso reduced the risk of disease progression or death by 84% compared to placebo. Patients treated with the drug experienced a median progression-free survival of 39.1 months compared with 5.6 months for patients in the placebo group. The drugs’ safety and tolerability profiles were consistent with prior studies and no new safety concerns were identified.Last month, the EMA’s advisory committee adopted a positive opinion, recommendi","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/spvq99_pwlnf7s60ZXBlKg--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/06708d71c63051ca48bf1855727f077b","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/spvq99_pwlnf7s60ZXBlKg--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/06708d71c63051ca48bf1855727f077b"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/azns-tagrisso-gets-approval-eu-155600638.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":["BK4196","BK4007","LU2236285917.USD","AZN","BK4139","LU0109394709.USD","SPRO","LU2462157665.USD","BK4585","BK4588","CSTL","BK4156","LU0889565916.HKD","LU2456880835.USD","BK4568","LU1829250122.USD","LU0320765992.SGD","CTMX","LU2417539215.USD"],"gpt_icon":0},{"id":"2493424389","title":"VRTX Down as Non-Opioid Drug Shows Similar Pain Reduction as Placebo","url":"https://stock-news.laohu8.com/highlight/detail?id=2493424389","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493424389?lang=en_us&edition=fundamental","pubTime":"2024-12-21 00:13","pubTimestamp":1734711180,"startTime":"0","endTime":"0","summary":"Shares of Vertex Pharmaceuticals Incorporated VRTX were down 11.4% yesterday after the company announced data from a phase II study that evaluated its investigational, oral, highly selective NaV1.8 pain signal inhibitor, suzetrigine, for treating people with painful lumbosacral radiculopathy , a form of peripheral neuropathic pain.Data from the study showed that treatment with suzetrigine led to a statistically significant and clinically meaningful within-group reduction in pain from baseline with a mean change in numeric pain rating scale of -2.02 at week 12, thereby meeting the primary endpoint.However, the placebo arm demonstrated a similar reduction of -1.98 points, indicating not much difference between the two groups.Shares of VRTX were down as investors were not too impressed with the data as it does not clearly demonstrate suzetrigine’s benefit-risk profile.Year to date, shares of Vertex have lost 2.5% compared with the industry’s decline of 13.7%.However, the disappointing dat","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/.WQmSb1MJO1_eLnmBVS1zA--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/a1d7049b0977a02a21fd2aa02b46f307","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/.WQmSb1MJO1_eLnmBVS1zA--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/a1d7049b0977a02a21fd2aa02b46f307"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/vrtx-down-non-opioid-drug-161300244.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":["LU0234570918.USD","IE00B19Z3581.USD","LU0566484027.USD","IE0009355771.USD","LU0256863811.USD","LU2417539215.USD","IE00B2B36J28.USD","LU2362541513.USD","IE00BJT1NW94.SGD","IE0002270589.USD","LU0058720904.USD","LU2236285917.USD","LU1585245621.USD","CSTL","IE00B19Z9P08.USD","LU0823416689.USD","LU2237438978.USD","VERX","IE00BFTCPJ56.SGD","LU0889565916.HKD","BK4532","IE00B19Z3B42.SGD","IE00BZ9MQY76.HKD","LU1093756168.USD","BK4567","LU0079474960.USD","LU0320765992.SGD","IE00B19Z9Z06.USD","LU0061475181.USD","LU1093756325.SGD","VRTX","LU1559883803.SGD","IE00B894F039.SGD","LU0109394709.USD","BK4533","BK4585","LU1035775433.USD","LU2362540622.SGD","LU2456880835.USD","BK4588","LU2462157665.USD","LU2362541273.HKD","SPRO","IE00BJJMRZ35.SGD","LU1430594728.SGD","IE00B4R5TH58.HKD","LU2324357040.USD","LU1069344957.HKD","BK4023","CTMX"],"gpt_icon":0},{"id":"2492025121","title":"KRYS Reports Upbeat Initial Data From Lung Cancer Study of KB707","url":"https://stock-news.laohu8.com/highlight/detail?id=2492025121","media":"Zacks","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2492025121?lang=en_us&edition=fundamental","pubTime":"2024-12-20 00:08","pubTimestamp":1734624480,"startTime":"0","endTime":"0","summary":"Krystal BiotechKRYS announced encouraging initial clinical data from an early to mid-stage study of its investigational immunotherapy candidate, KB707, to treat patients with solid tumors of the lung.The phase I/II KYANITE-1 study is evaluating the safety, tolerability and tumor response  of inhaled KB707 as a monotherapy in 37 patients with malignant lesions in the lung. Out of the total enrolled patient population, 17 were diagnosed with advanced non-small cell lung cancer . Two doses of KB707  were evaluated during the dose-escalation phase of the KYANITE-1 study, following which 109PFU was selected for dose expansion.Results showed that patients treated with inhaled KB707 demonstrated early evidence of monotherapy activity with the most therapeutic benefit observed in advanced NSCLC patients, who have progressed after standard-of-care treatments.In the past three months, shares of Krystal Biotech have lost 14.9% compared with theindustry’s 13.3% decline.KB707 is also being develope","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/2NHx6klCutBjAlMNJEM7HQ--~B/aD00MTM7dz02MjA7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/b5aeac1c53d022d48463312844fb1baf","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/2NHx6klCutBjAlMNJEM7HQ--~B/aD00MTM7dz02MjA7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/b5aeac1c53d022d48463312844fb1baf"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/krys-reports-upbeat-initial-data-160800963.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":["BK4139","BK4196","SPRO","CSTL","KRYS","CTMX"],"gpt_icon":0},{"id":"2492174258","title":"SRPT Finishes Enrolment in Late-Stage Study for Rare Muscular Disorder","url":"https://stock-news.laohu8.com/highlight/detail?id=2492174258","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2492174258?lang=en_us&edition=fundamental","pubTime":"2024-12-19 21:45","pubTimestamp":1734615900,"startTime":"0","endTime":"0","summary":"Sarepta Therapeutics SRPT announced that it has completed enrolment and dosing in the phase III EMERGENE study evaluating its investigational gene therapy, SRP-9003  for treating limb-girdle muscular dystrophy  Type 2E/R4 .Data from the EMERGENE study is expected in the first half of 2025. If the data is positive, Sarepta intends to submit a regulatory filing seeking accelerated approval for SRP-9003 in the given indication before the end of next year.The primary endpoint of the study is the biomarker expression of the beta-sarcoglycan protein, whose absence is the sole cause of the disease.LGMD2E/R4 is an ultra-rare form of LGMD for which there is no treatment beyond symptom management. Patients suffering from this genetic disease exhibit neuromuscular symptoms, which include difficulty in running, jumping and climbing stairs, before the age of 10. Because of the lack of treatments, the disease often progresses to loss of mobility during the teenage years and is associated with early ","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/2ZuhDuDie_37lq4aVERX2Q--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/4718122d03716403704541c667907c4e","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/2ZuhDuDie_37lq4aVERX2Q--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/4718122d03716403704541c667907c4e"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/srpt-finishes-enrolment-stage-study-134500600.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":["03165","CTMX","IE0009355771.USD","IE00BFTCPJ56.SGD","IE00BJJMRZ35.SGD","SRPT","BK4196","IE00B2B36J28.USD","RHHBY","BK4585","BK4007","IE00BJT1NW94.SGD","IE0002141913.USD","SSI","CSTL","BK4139"],"gpt_icon":0},{"id":"2492135482","title":"GILD's Trodelvy Gets Second Breakthrough Therapy Tag for Lung Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2492135482","media":"Zacks","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2492135482?lang=en_us&edition=fundamental","pubTime":"2024-12-18 23:14","pubTimestamp":1734534840,"startTime":"0","endTime":"0","summary":"Gilead SciencesGILD announced that its first-in-class Trop-2-directed antibody-drug conjugate, Trodelvy, has been granted a second Breakthrough Therapy designationby the FDA for a lung cancer indication. The indicated population includes adult patients with extensive-stage small cell lung cancer  whose disease has progressed on or after platinum-based chemotherapy.Gilead’s Trodelvy is currently approved for second-line or later metastatic triple-negative breast cancer  patients in more than 50 countries and for certain patients with pre-treated HR+/HER2- metastatic breast cancer  in more than 40 countries, including the United States. The first Breakthrough Therapy designation was granted to Trodelvy for the TNBC indication in the United States.Benefits of the FDA’s Breakthrough Therapy Designation Grant. The FDA’s Breakthrough Therapy designation is a process that speeds up the development and review of drugs for serious or life-threatening conditions. This designation is granted 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