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Checkpoint Therapeutics, Inc.

4.04

+0.0000

Post-market: 4.040.00000.00%16:05 EDT

Volume:3.95M

Turnover:15.85M

Market Cap:338.41M

PE:-2.85

High:4.05

Open:3.99

Low:3.98

Close:4.04

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Overview Company News Filings

Unusually active option classes on open December 16th

Checkpoint Therapeutics Shares Rise 5.7% After US FDA Approves Co's Skin Cancer Drug

THOMSON REUTERS

FDA Approves Checkpoint Therapeutics' Skin Cancer Drug One Year After Rejection

Pre-Bell｜U.S. Futures Rise; Tesla Gains 1%; Broadcom and MicroStrategy Jump 3%; Super Micro Plunges 13%

Tiger Newspress

Checkpoint Therapeutics Price Target Maintained With a $20.00/Share by HC Wainwright & Co.

Analysts Offer Insights on Healthcare Companies: Checkpoint Therapeutics (CKPT) and Roche Holding AG (OtherRHHVF)

BUZZ-Checkpoint Therapeutics rises after FDA approval of co's skin cancer drug

Checkpoint Therapeutics Shares Rise 9.3% Premarket After US FDA Approves Co's Skin Cancer Drug

THOMSON REUTERS

Checkpoint Therapeutics' Shares Rise After Securing First FDA Approval

Checkpoint Therapeutics trading resumes

Checkpoint Therapeutics confirms FDA approval of unloxcyt

Checkpoint Therapeutics Gets Its First FDA Approval

BRIEF-Checkpoint Therapeutics Announces FDA Approval Of Unloxcyt (Cosibelimab-Ipdl)

US FDA approves Checkpoint's skin cancer drug

FDA Approves Cosibelimab-Ipdl for Metastatic or Locally Advanced Cutaneous Squamous Cell Carcinoma - Website

THOMSON REUTERS

FDA: Approval of Cosibelimab-Ipdl (Unloxcyt) Granted to Checkpoint Therapeutics

THOMSON REUTERS

Checkpoint Therapeutics trading halted, news pending

Checkpoint Therapeutics Price Target Maintained With a $20.00/Share by HC Wainwright & Co.

Checkpoint Therapeutics Third Quarter 2024 Earnings: US$0.23 loss per share (vs US$0.29 loss in 3Q 2023)

Simply Wall St.

Checkpoint Therapeutics Q3 2024 GAAP EPS $(0.23) Misses $(0.16) Estimate

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commercial-stage company, with the opportunity to compete in a U.S. market estimated to exceed $1 billion annually, where we believe Unloxcyt offers a differentiated treatment option versus available therapies,” said James Oliviero, President and Chief Executive Officer of Checkpoint.FDA approval for Unloxcyt was granted based ","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/Yojrtf9mwvY24CWG5yK_2A--~B/aD01NjM7dz0xMDAwO2FwcGlkPXl0YWNoeW9u/https://media.zenfs.com/en/Benzinga/6697296d010bda0215dda8265751ec8f","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/Yojrtf9mwvY24CWG5yK_2A--~B/aD01NjM7dz0xMDAwO2FwcGlkPXl0YWNoeW9u/https://media.zenfs.com/en/Benzinga/6697296d010bda0215dda8265751ec8f"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/fda-approves-checkpoint-therapeutics-skin-142201452.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":["BK4530","BK4139","BK4585","CRL","BK4588","LU0390134368.USD","BK4121","CKPT","LENZ"],"gpt_icon":0},{"id":"1169868872","title":"Pre-Bell｜U.S. Futures Rise; Tesla 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after FDA approval of co's skin cancer drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2491661366","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2491661366?lang=en_us&edition=fundamental","pubTime":"2024-12-16 19:25","pubTimestamp":1734348321,"startTime":"0","endTime":"0","summary":"BUZZ-Checkpoint Therapeutics rises after FDA approval of co's skin cancer drug ** Shares of drug developer Checkpoint Therapeutics CKPT.O rise 8.9% to $4 in premarket trading** The U.S. FDA, on Friday, approved company's drug for treatment of a type of cancer of the outer layer of the skin** The drug to be marketed under the brand name Unloxcyt is the company's first drug that has received approval** Unloxcyt is part of a class of drugs, PD-L1 antibody, which works by binding to a protein called programmed death-ligand 1 that helps the body's immune system in killing cancer cells** Company said it is \"currently developing a commercial launch plan\" for the drug ** Up to last close, stock up 60.3% YTD   ","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:20241216:nL4N3NH0QI: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":["CKPT","BK4139","FBIO"],"gpt_icon":0},{"id":"2491466994","title":"Checkpoint Therapeutics Shares Rise 9.3% Premarket After US FDA Approves Co's Skin Cancer Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2491466994","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2491466994?lang=en_us&edition=fundamental","pubTime":"2024-12-16 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08:09","pubTimestamp":1734134940,"startTime":"0","endTime":"0","summary":"Shares of Checkpoint Therapeutics rose 4.6% to $3.84 in post-market trading after the Food and Drug Administration approved Unloxcyt  for advanced cutaneous squamous cell carcinoma, the first-ever approval for the company.Checkpoint said in July the FDA accepted for review its resubmission of the Biologics License Application and set a Prescription Drug User Fee Act goal date of Dec. 28.The agency issued a Complete Response Letter for the application in December 2023. The letter cited findings that arose during a multi-sponsor inspection of Checkpoint's third-party contract manufacturer. The letter didn't state any concerns about the clinical data package, safety, or labeling for the approvability of cosibelimab, the company said at the time.Checkpoint said it believes Unloxcyt offers a differentiated treatment option versus available therapies by binding to PD-L1, rather than PD-1, to release the inhibitory effects of PD-L1 as part of the anti-tumor immune response.The approval provid","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","LENZ","CKPT"],"gpt_icon":1},{"id":"2491873065","title":"Checkpoint Therapeutics trading 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fina...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/checkpoint-therapeutics-trading-resumes?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/checkpoint-therapeutics-trading-resumes?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":["BK4139","CKPT","LENZ"],"gpt_icon":0},{"id":"2491587302","title":"Checkpoint Therapeutics confirms FDA approval of unloxcyt","url":"https://stock-news.laohu8.com/highlight/detail?id=2491587302","media":"TIPRANKS","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2491587302?lang=en_us&edition=fundamental","pubTime":"2024-12-14 07:35","pubTimestamp":1734132925,"startTime":"0","endTime":"0","summary":"Checkpoint Therapeutics (CKPT) announced that the U.S. FDA has approved unloxcyt for the treatment of adults with metastatic cutaneous squamous cel...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/checkpoint-therapeutics-confirms-fda-approval-of-unloxcyt?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/checkpoint-therapeutics-confirms-fda-approval-of-unloxcyt?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":["BK4139","LENZ","CKPT"],"gpt_icon":0},{"id":"2491192582","title":"Checkpoint Therapeutics Gets Its First FDA Approval","url":"https://stock-news.laohu8.com/highlight/detail?id=2491192582","media":"Dow Jones","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2491192582?lang=en_us&edition=fundamental","pubTime":"2024-12-14 07:29","pubTimestamp":1734132540,"startTime":"0","endTime":"0","summary":"Checkpoint Therapeutics said the Food and Drug Administration approved Unloxcyt  for advanced cutaneous squamous cell carcinoma, the company's first approval.Checkpoint said in July that the FDA accepted for review its resubmission of the Biologics License Application for the drug and set a Prescription Drug User Fee Act goal date of Dec. 28.Shares were up 3.3% to $3.79 after hours prior to being halted due to pending news.","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LENZ","CKPT","BK4139"],"gpt_icon":0},{"id":"2491828785","title":"BRIEF-Checkpoint Therapeutics Announces FDA Approval Of Unloxcyt (Cosibelimab-Ipdl)","url":"https://stock-news.laohu8.com/highlight/detail?id=2491828785","media":"Reuters","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2491828785?lang=en_us&edition=fundamental","pubTime":"2024-12-14 07:17","pubTimestamp":1734131825,"startTime":"0","endTime":"0","summary":"BRIEF-Checkpoint Therapeutics Announces FDA Approval Of UnloxcytDec 13  - Checkpoint Therapeutics Inc CKPT.O:CHECKPOINT THERAPEUTICS ANNOUNCES FDA APPROVAL OF UNLOXCYT Source text: nGNX3Mnqk6Further company coverage: CKPT.O ","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:20241213:nTUA2K6LJS:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["FBIO","BK4139","CKPT"],"gpt_icon":0},{"id":"2491780584","title":"US FDA approves Checkpoint's skin cancer drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2491780584","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2491780584?lang=en_us&edition=fundamental","pubTime":"2024-12-14 07:11","pubTimestamp":1734131475,"startTime":"0","endTime":"0","summary":"Dec 13 (Reuters) - The U.S Food and Drug Administration said on Friday it has approved Checkpoint Therapeutics'    drug for treatment of two types of skin cancer. (Reporting by Leroy Leo in Bengaluru; Editing by Krishna Chandra Eluri)((Leroy.Dsouza@thomsonreuters.com;))","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":"2","news_top_title":"US FDA approves Checkpoint's skin cancer drug","news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CKPT","BK4139"],"gpt_icon":0},{"id":"2491841985","title":"FDA Approves Cosibelimab-Ipdl for Metastatic or Locally Advanced Cutaneous Squamous Cell Carcinoma - Website","url":"https://stock-news.laohu8.com/highlight/detail?id=2491841985","media":"THOMSON 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