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Nuvation Bio, Inc.

2.46

+0.19008.37%

Post-market: 2.470.0100+0.41%18:45 EDT

Volume:5.90M

Turnover:14.43M

Market Cap:835.58M

PE:-1.16

High:2.54

Open:2.31

Low:2.31

Close:2.27

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Overview Company News Filings

Nuvation Bio's Taletrectinib Secures Approval in China for Lung Cancer Treatment

MT Newswires Live

BRIEF-Nuvation Bio Receives Approval From China's National Medical Products Administration For Taletrectinib For Patients With Advanced ROS1-Positive Non-Small Cell Lung Cancer

Nuvation Bio Inc - Taletrectinib to Be Marketed in China by Innovent Biologics

THOMSON REUTERS

Nuvation Bio Receives Approval From China’s National Medical Products Administration for Taletrectinib for Patients With Advanced Ros1-Positive Non-Small Cell Lung Cancer

THOMSON REUTERS

Nuvation Bio Receives Approval from China’s National Medical Products Administration for Taletrectinib for Patients with Advanced ROS1-positive Non-Small Cell Lung Cancer

Nuvation Bio Price Target Maintained With a $7.00/Share by HC Wainwright & Co.

Why Is Nuvation Bio (NUVB) the Best Biotech Penny Stock to Invest in Now?

Sector Update: Health Care Stocks Fall Premarket Monday

MT Newswires Live

Nuvation Bio's Lung Cancer Drug Candidate Taletrectinib Gets FDA Priority Review

MT Newswires Live

FDA accepts Nuvation Bio’s NDA for taletrectinib to treat ROS1+NSCLC

Nuvation Bio Inc - FDA Assigns Target Action Date of June 23, 2025

THOMSON REUTERS

U.S. Food and Drug Administration Accepts for Priority Review Nuvation Bio’s New Drug Application for Taletrectinib for the Treatment of Advanced Ros1-Positive Non-Small Cell Lung Cancer

THOMSON REUTERS

U.S. Food and Drug Administration Accepts for Priority Review Nuvation Bio’s New Drug Application for Taletrectinib for the Treatment of Advanced ROS1-positive Non-Small Cell Lung Cancer

Innovent Receives Approval of Dovbleron® (Taletrectinib Adipate Capsule, Ros1 Inhibitor) by China's National Medical Products Administration

THOMSON REUTERS

Nuvation Bio to Present at the 7th Annual Evercore ISI HealthCONx Conference

Is Nuvation Bio (NYSE:NUVB) Using Debt In A Risky Way?

Simply Wall St.

Nuvation Bio to Present at the Jefferies London Healthcare Conference

Nuvation Bio’s Global Challenges: Navigating Risks in China Amid Geopolitical Tensions

Nuvation Bio Is Maintained at Outperform by RBC Capital

RBC Capital Adjusts Price Target on Nuvation Bio to $6 From $5, Maintains Outperform, Speculative Risk Rating

MT Newswires Live

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Nuvation Bio Inc   :   * NUVATION BIO RECEIVES APPROVAL FROM CHINA’S NATIONAL MEDICAL PRODUCTS ADMINISTRATION FOR TALETRECTINIB FOR PATIENTS WITH ADVANCED ROS1-POSITIVE NON-SMALL CELL LUNG CANCER   * NUVATION BIO INC - TALETRECTINIB TO BE MARKETED IN CHINA BY INNOVENT BIOLOGICSSource text:   Further company coverage:    ","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://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_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":["NUVB","AEIS","NHLD","BK4007","IE0031619046.USD","BK4157","IE00B66KJ199.SGD","IE00B19Z4B17.USD","IE00B7SZL793.SGD"],"gpt_icon":0},{"id":"2501366239","title":"Nuvation Bio Inc - Taletrectinib to Be Marketed in China by Innovent Biologics","url":"https://stock-news.laohu8.com/highlight/detail?id=2501366239","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2501366239?lang=en_us&edition=fundamental","pubTime":"2025-01-06 21:00","pubTimestamp":1736168407,"startTime":"0","endTime":"0","summary":null,"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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250106:nTUA7FBJK9:2","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":"reuters_en_live","symbols":["BK4007","NUVB"],"gpt_icon":0},{"id":"2501348239","title":"Nuvation Bio Receives Approval From China’s National Medical Products Administration for Taletrectinib for Patients With Advanced Ros1-Positive Non-Small Cell Lung Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2501348239","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2501348239?lang=en_us&edition=fundamental","pubTime":"2025-01-06 21:00","pubTimestamp":1736168407,"startTime":"0","endTime":"0","summary":null,"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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250106:nTUA7FBJK9:1","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":"reuters_en_live","symbols":["NUVB","BK4007"],"gpt_icon":0},{"id":"2501239268","title":"Nuvation Bio Receives Approval from China’s National Medical Products Administration for Taletrectinib for Patients with Advanced ROS1-positive Non-Small Cell Lung Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2501239268","media":"Business Wire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2501239268?lang=en_us&edition=fundamental","pubTime":"2025-01-06 21:00","pubTimestamp":1736168400,"startTime":"0","endTime":"0","summary":"Taletrectinib will be marketed in China by Innovent Biologics. Approval is based on the pivotal Phase 2 TRUST-I study, demonstrating taletrectinib's durable responses and prolonged progression-free survival. NEW YORK, January 06, 2025----Nuvation Bio Inc. , a global biopharmaceutical company tackling some of the greatest unmet needs in oncology, today announced that China’s National Medical Products Administration  has approved taletrectinib for the treatment of adult patients with locally advanced or metastatic ROS1-positive  non-small cell lung cancer  who either have or have not been previously treated with ROS1 tyrosine kinase inhibitors . As part of an exclusive license agreement, Innovent Biologics will commercialize taletrectinib in China under the brand name DOVBLERON. The product was officially launched in the territory in January 2025. Taletrectinib was previously granted Breakthrough Therapy Designation and Priority Review by China’s NMPA.Taletrectinib is an oral, potent, ce","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/nuvation-bio-receives-approval-china-130000455.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":["IE0031619046.USD","BK4157","IE00B66KJ199.SGD","NHLD","IE00B7SZL793.SGD","BK4212","AEIS","IE00B19Z4B17.USD","NUVB","DDC","BK4007"],"gpt_icon":0},{"id":"2501661238","title":"Nuvation Bio Price Target Maintained With a $7.00/Share by HC Wainwright & Co.","url":"https://stock-news.laohu8.com/highlight/detail?id=2501661238","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2501661238?lang=en_us&edition=fundamental","pubTime":"2025-01-06 19:55","pubTimestamp":1736164500,"startTime":"0","endTime":"0","summary":"Ratings actions from Benzinga: https://www.benzinga.com/quote/NUVB/analyst-ratings \n\n\n \n\n\n  (END) Dow Jones Newswires\n\n\n  January 06, 2025 06:55 ET (11:55 GMT)","market":"hk","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":["NUVB"],"gpt_icon":0},{"id":"2495563570","title":"Why Is Nuvation Bio (NUVB) the Best Biotech Penny Stock to Invest in Now?","url":"https://stock-news.laohu8.com/highlight/detail?id=2495563570","media":"Insider Monkey","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2495563570?lang=en_us&edition=fundamental","pubTime":"2024-12-31 04:00","pubTimestamp":1735588833,"startTime":"0","endTime":"0","summary":"We recently published a list of the 12 Best Biotech Penny Stocks To Invest In Now. In this article, we are going to take a look at where Nuvation Bio Inc.  stands against the other best biotech penny stocks to invest in now.Sears noted that small and emerging biotechnology companies have been at the forefront of this innovation. In 2023, approximately two-thirds of all clinical trials were initiated by small and emerging biotechnology firms, and about 56% of new drug substances approved by regulatory bodies originated from these smaller compani","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/why-nuvation-bio-nuvb-best-200033701.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":["LU0106831901.USD","LU2237438978.USD","BK4552","LU2237443382.USD","BK4588","BK4127","BK4504","IE0002270589.USD","IE0004091025.USD","LU1668664300.SGD","BK4007","IE00B19Z3B42.SGD","IE0034235188.USD","IE00B19Z3581.USD","BK4585","LU2237443549.SGD","IE00BSNM7G36.USD","LU2237443465.HKD","BK4550","LU2237443622.USD","LU2237443978.SGD","NUVB","IE0004086264.USD","LU1791807156.HKD","BK4533","LU2237443895.HKD","IE00BFXG1179.USD","BK4516"],"gpt_icon":1},{"id":"2493637867","title":"Sector Update: Health Care Stocks Fall Premarket Monday","url":"https://stock-news.laohu8.com/highlight/detail?id=2493637867","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493637867?lang=en_us&edition=fundamental","pubTime":"2024-12-23 22:21","pubTimestamp":1734963689,"startTime":"0","endTime":"0","summary":"Health care stocks fell premarket Monday with the Health Care Select Sector SPDR Fund  down marginally and the iShares Biotechnology ETF  0.5% lower recently.Alvotech  shares were up more than 5% after the company said it has been added to the Nasdaq Biotechnology Index, effective at market open.Nuvation Bio  shares advanced by over 7% after the company said the US Food and Drug Administration has accepted its new drug application for drug candidate taletrectinib intended for the treatment of non-small cell lung cancer.Eli Lilly  shares were 2% higher after the company said the US Food and Drug Administration approved its tirzepatide product Zepbound as the first and only prescription medicine for moderate-to-severe obstructive sleep apnea and obesity.","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://www.mtnewswires.com/","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":"mtnewswires_news","symbols":["IE00BFTCPJ56.SGD","IE00BK4W5L77.USD","LU1127390331.HKD","LLY","SGXZ31699556.SGD","LU2361044865.SGD","LU0061475181.USD","ALVO","BK4139","SG9999015952.SGD","SGXZ99366536.SGD","NUVB","LU0882574139.USD","SG9999014906.USD","LU2360106947.USD","LU1093756325.SGD","LU0203202063.USD","LU1868836757.USD","BK4534","LU1712237335.SGD","LU0238689110.USD","IE00BJJMRZ35.SGD","LU2264538146.SGD","LU2063271972.USD","LU0006306889.USD","SGXZ57979304.SGD","XLV","LU2468319806.SGD","LU1551013425.SGD","SGXZ81514606.USD","SG9999014914.USD","IE00B2B36J28.USD","IBB","LU0417517546.SGD","LU2237443622.USD","LU0094547139.USD","GB00BDT5M118.USD","IE00B1BXHZ80.USD","BK4516","IE00BK4W5M84.HKD","LU2089984988.USD","LU2491050071.SGD","LU0708995401.HKD","LU2361045086.USD","LU0471298777.SGD","LU0466842654.USD","LU1069344957.HKD","LU1804176565.USD","SG9999001176.SGD","LU1064131342.USD"],"gpt_icon":1},{"id":"2493750633","title":"Nuvation Bio's Lung Cancer Drug Candidate Taletrectinib Gets FDA Priority Review","url":"https://stock-news.laohu8.com/highlight/detail?id=2493750633","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493750633?lang=en_us&edition=fundamental","pubTime":"2024-12-23 21:37","pubTimestamp":1734961072,"startTime":"0","endTime":"0","summary":"Nuvation Bio  said Monday the US Food and Drug Administration has accepted its new drug application for drug candidate taletrectinib intended for the treatment of non-small cell lung cancer.The FDA granted priority review and set a Prescription Drug User Fee Act goal date of June 23, Nuvation said.Nuvation stock was up more than 4% in recent premarket activity.Price: 2.80, Change: +0.12, Percent Change: +4.48","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4007","NUVB"],"gpt_icon":0},{"id":"2493757970","title":"FDA accepts Nuvation Bio’s NDA  for taletrectinib to treat ROS1+NSCLC","url":"https://stock-news.laohu8.com/highlight/detail?id=2493757970","media":"TIPRANKS","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493757970?lang=en_us&edition=fundamental","pubTime":"2024-12-23 21:10","pubTimestamp":1734959439,"startTime":"0","endTime":"0","summary":"Nuvation Bio (NUVB) announced that the U.S. FDA has accepted the company’s NDA for taletrectinib, an investigational next-generation ROS1 tyrosine ...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/fda-accepts-nuvation-bios-nda-for-taletrectinib-to-treat-ros1nsclc?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/fda-accepts-nuvation-bios-nda-for-taletrectinib-to-treat-ros1nsclc?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["BK4007","NUVB"],"gpt_icon":0},{"id":"2493525557","title":"Nuvation Bio Inc - FDA Assigns Target Action Date of June 23, 2025","url":"https://stock-news.laohu8.com/highlight/detail?id=2493525557","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493525557?lang=en_us&edition=fundamental","pubTime":"2024-12-23 21:00","pubTimestamp":1734958802,"startTime":"0","endTime":"0","summary":null,"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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20241223:nTUA8WMN5G:2","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":"reuters_en_live","symbols":["NUVB","BK4007"],"gpt_icon":0},{"id":"2493375258","title":"U.S. Food and Drug Administration Accepts for Priority Review Nuvation Bio’s New Drug Application for Taletrectinib for the Treatment of Advanced Ros1-Positive Non-Small Cell Lung Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2493375258","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493375258?lang=en_us&edition=fundamental","pubTime":"2024-12-23 21:00","pubTimestamp":1734958802,"startTime":"0","endTime":"0","summary":null,"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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20241223:nTUA8WMN5G:1","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":"reuters_en_live","symbols":["BK4007","NUVB"],"gpt_icon":0},{"id":"2493752770","title":"U.S. Food and Drug Administration Accepts for Priority Review Nuvation Bio’s New Drug Application for Taletrectinib for the Treatment of Advanced ROS1-positive Non-Small Cell Lung Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2493752770","media":"Business Wire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493752770?lang=en_us&edition=fundamental","pubTime":"2024-12-23 21:00","pubTimestamp":1734958800,"startTime":"0","endTime":"0","summary":"New Drug Application  is based on pooled data from the pivotal Phase 2 TRUST-I and TRUST-II studies of taletrectinib that demonstrated durable responses and prolonged progression-free survival in patients with advanced ROS1-positive  non-small cell lung cancer . If approved, taletrectinib represents a potential best-in-class treatment option for patients with advanced ROS1+ NSCLC. U.S. Food and Drug Administration  has assigned a target action date of June 23, 2025. Dr. Hung continued, \"Since acquiring AnHeart Therapeutics earlier this year, including taletrectinib, we have executed on our plan to advance taletrectinib toward a full U.S. regulatory approval. The FDA’s Priority Review reflects the strength of our clinical data and the promise taletrectinib holds for patients. 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