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Park Hotels & Resorts Inc.

15.16

-0.0550-0.36%

Volume:1.17M

Turnover:17.83M

Market Cap:3.05B

PE:-18.34

High:15.37

Open:15.27

Low:15.11

Close:15.21

52wk High:16.20

52wk Low:9.84

Shares:201.40M

Float Shares:195.63M

Volume Ratio:0.58

T/O Rate:0.60%

Dividend:1

Dividend Rate:6.60%

EPS(TTM):-0.8265

EPS(LYR):-1.4300

ROE:-4.86%

ROA:2.75%

PB:0.99

PE(LYR):-10.60

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Overview Company News Filings

Park Hotels & Resorts (PK) Is Up 9.1% After Strong Q1 RevPAR Beat And Non-Core Asset Sale

Simply Wall St.

Park Hotels & Resorts Is Maintained at Hold by Truist Securities

RenovoRx Announces Promising Pharmacokinetic Data Using the TAMP™ Platform Presented at the 2026 ASCO Annual Meeting

Truist Raises Price Target on Park Hotels & Resorts to $13 From $12, Keeps Hold Rating

MT Newswires Live

Agios’ PYRUKYND® (mitapivat) Approved in the European Union for Adults with Thalassemia

Syndax Announces Four Revuforj® (revumenib) Abstracts Accepted for ASCO 2026, Including an Oral Presentation of Post-Transplant Data

Amplia Therapeutics Launches First Stage of Registration-Enabling Trial of Narmafotinib

Propanc Biopharma Provides Corporate Update and Reports Third Quarter 2025/26 Results

Press Release: Alpha Cognition Inc. Reports First Quarter 2026 Financial Results and Provides Operational Update

Galmed reports results from first-in-man PK study of Aramchol Meglumine

Press Release: Oruka Therapeutics Reports First Quarter 2026 Financial Results and Provides Corporate Update

Park Hotels & Resorts Price Target Maintained With a $12.00/Share by Cantor Fitzgerald

Atea Pharmaceuticals Reports First Quarter 2026 Financial Results and Provides Business Update

Park Hotels & Resorts Is Maintained at Equal-Weight by Morgan Stanley

Agios Submits sNDA to FDA for U.S. Accelerated Approval of Mitapivat in Sickle Cell Disease

Ovid Therapeutics Reports Business Updates and First Quarter 2026 Financial Results

Press Release: Sionna Therapeutics Reports First Quarter 2026 Financial Results

Erasca Reports First Quarter 2026 Business Updates and Financial Results

MBX Biosciences Provides Obesity Portfolio Update Including Initial Phase 1 Data for MBX 4291 Supporting Potential for Once-Monthly Dosing

Press Release: Actuate Therapeutics Announces FDA Clearance of IND for Oral Elraglusib and Strategic Initiatives to Advance the Elraglusib Development Program

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for adults with transfusion-dependent and non-transfusion-dependent alpha- or beta-thalassemiaMitapivat is now approved for thalassemia in the U.S., Sa","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2026/05/22/3300143/31990/en/Agios-PYRUKYND-mitapivat-Approved-in-the-European-Union-for-Adults-with-Thalassemia.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":null,"symbols":["BK4181","RBC","EC","LU2065731478.USD","EPV","BK4201","BK4161","IE00B64QTZ34.USD","PK","BK4156","BK4218","IE00BD6J9T35.USD","IE00BLDYK493.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2637357561","title":"Syndax Announces Four Revuforj® (revumenib) Abstracts Accepted for 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Cash and cash equivalents totaled $54 million as of March 31, 2026, supporting the Company's continued target of operating profitability in 2027. Company to host conference call and webcast today, May 14, at 4:30 p.m. ET. Alpha Cognition Inc.  , a biopharmaceutical company developing novel therapeutics for debilitating neurodegenerative disorders, today reported financial results for the first quarter ended March 31, 2026, and provided a business update.p","market":"other","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":"0","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","BK4218","ACOG","PK","BK4181"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635712585","title":"Galmed reports results from first-in-man PK study of Aramchol Meglumine","url":"https://stock-news.laohu8.com/highlight/detail?id=2635712585","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2635712585?lang=en_us&edition=fundamental","pubTime":"2026-05-14 19:53","pubTimestamp":1778759584,"startTime":"0","endTime":"0","summary":"Galmed (GLMD) announced milestone results from a Phase 1 PK study in healthy subjects. The overall objective of the study was to identify the dose ...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/galmed-reports-results-from-first-in-man-pk-study-of-aramchol-meglumine-thefly-news?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/galmed-reports-results-from-first-in-man-pk-study-of-aramchol-meglumine-thefly-news?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":["PK","GLMD","BK4139","BK4218","BK4181"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635941758","title":"Press Release: Oruka Therapeutics Reports First Quarter 2026 Financial Results and Provides Corporate Update","url":"https://stock-news.laohu8.com/highlight/detail?id=2635941758","media":"Dow Jones","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2635941758?lang=en_us&edition=fundamental","pubTime":"2026-05-14 04:03","pubTimestamp":1778702580,"startTime":"0","endTime":"0","summary":"ORKA-001 EVERLAST-A 16-week data showed 63.5% PASI 100 rate and a favorable tolerability profile, with longer-term data expected in 2H 2026. ORCA-SURGE Phase 2 trial of ORKA-002 in psoriasis initiated with data expected 2027. Post-offering cash, cash equivalents and marketable securities expected to fund Company through BLA for ORKA-001. MENLO PARK, Calif., May 13, 2026  -- Oruka Therapeutics, Inc.  , a clinical-stage biotechnology company developing novel biologics designed to set a new standard for the treatment of chronic skin diseases including plaque psoriasis , today reported first quarter 2026 financial results and provided a corporate update.\"This was an important period for our company as we saw interim data for ORKA-001 that hit the upper end of our expectations on all aspects,\" said Lawrence Klein, PhD, Chief Executive Officer of Oruka. \"Based on this data we were able to strengthen our balance sheet and provide runway through completion of late-stage development for that pr","market":"sg","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":"0","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["TM","BK4218","LU1169590202.USD","BK4604","BK4023","LU1169589451.USD","03160","LENZ","BK4585","BK4588","BK4555","BK4139","BK4099","BK4007","ORKA","PD","PK","BK4539","BK4181"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635378032","title":"Park Hotels & Resorts Price Target Maintained With a $12.00/Share by Cantor Fitzgerald","url":"https://stock-news.laohu8.com/highlight/detail?id=2635378032","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2635378032?lang=en_us&edition=fundamental","pubTime":"2026-05-13 21:17","pubTimestamp":1778678220,"startTime":"0","endTime":"0","summary":"Ratings actions from Benzinga: https://www.benzinga.com/quote/PK/analyst-ratings \n\n\n \n\n\n  (END) Dow Jones Newswires\n\n\n  May 13, 2026 09:17 ET (13:17 GMT)","market":"sg","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["PK","BK4181","BK4218"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635240589","title":"Atea Pharmaceuticals Reports First Quarter 2026 Financial Results and Provides Business Update","url":"https://stock-news.laohu8.com/highlight/detail?id=2635240589","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2635240589?lang=en_us&edition=fundamental","pubTime":"2026-05-13 04:05","pubTimestamp":1778616300,"startTime":"0","endTime":"0","summary":"C-BEYOND Phase 3 North American Trial for Treatment of Hepatitis C Virus (HCV) Remains on Track with Topline Results Expected Mid-2026 C-FORWARD Phase 3 Trial Outside North America for Treatment of HC","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2026/05/12/3293389/0/en/Atea-Pharmaceuticals-Reports-First-Quarter-2026-Financial-Results-and-Provides-Business-Update.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["SOF","BK4218","BK4007","PK","BK4181","AVIR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635249185","title":"Park Hotels & Resorts Is Maintained at Equal-Weight by Morgan Stanley","url":"https://stock-news.laohu8.com/highlight/detail?id=2635249185","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2635249185?lang=en_us&edition=fundamental","pubTime":"2026-05-13 01:15","pubTimestamp":1778606100,"startTime":"0","endTime":"0","summary":"Ratings actions from Benzinga: https://www.benzinga.com/quote/PK/analyst-ratings \n\n\n \n\n\n  (END) Dow Jones Newswires\n\n\n  May 12, 2026 13:15 ET (17:15 GMT)","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://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":["BK4218","BK4181","PK"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634217337","title":"Agios Submits sNDA to FDA for U.S. Accelerated Approval of Mitapivat in Sickle Cell Disease","url":"https://stock-news.laohu8.com/highlight/detail?id=2634217337","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2634217337?lang=en_us&edition=fundamental","pubTime":"2026-05-12 21:31","pubTimestamp":1778592660,"startTime":"0","endTime":"0","summary":"sNDA submission follows agreement with FDA on confirmatory trial, a requirement of the accelerated approval pathway Confirmatory trial designed to demonstrate clinical benefit of mitapivat on reducing","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2026/05/12/3293011/31990/en/Agios-Submits-sNDA-to-FDA-for-U-S-Accelerated-Approval-of-Mitapivat-in-Sickle-Cell-Disease.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":null,"symbols":["BK4218","BK4585","LABU","BK4588","BK4181","PK"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634721329","title":"Ovid Therapeutics Reports Business Updates and First Quarter 2026 Financial Results","url":"https://stock-news.laohu8.com/highlight/detail?id=2634721329","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2634721329?lang=en_us&edition=fundamental","pubTime":"2026-05-12 19:00","pubTimestamp":1778583600,"startTime":"0","endTime":"0","summary":"Dosed first participant with OV4071, the first-ever oral potassium-chloride cotransporter 2 (KCC2) direct activator, in May 2026 in a Phase 1 study with healthy volunteersOV329 showed favorable safety","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2026/05/12/3292680/0/en/Ovid-Therapeutics-Reports-Business-Updates-and-First-Quarter-2026-Financial-Results.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4097","BK4218","BK4539","BK4585","BK4007","IS","BK4139","LENZ","APA","LU0256331488.USD","BK4213","BK4181","PK","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634218216","title":"Press Release: Sionna Therapeutics Reports First Quarter 2026 Financial Results","url":"https://stock-news.laohu8.com/highlight/detail?id=2634218216","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2634218216?lang=en_us&edition=fundamental","pubTime":"2026-05-12 19:00","pubTimestamp":1778583600,"startTime":"0","endTime":"0","summary":"Enrollment completed in the PreciSION CF Phase 2a proof-of-concept trial evaluating NBD1 stabilizer SION-719 as an add-on to standard of care in participants with cystic fibrosis; topline data on track for the summer of 2026. Ongoing Phase 1 trial evaluating NBD1 stabilizer SION-451 in proprietary dual combinations with SION-2222 and with SION-109 in healthy volunteers is also on track for topline data in the summer of 2026. Maintained strong cash position with approximately $289.9 million in cash and cash equivalents, expected to fund operations into 2028. \"We entered 2026 with strong execution across our programs, highlighted by the recent completion of enrollment in our proof-of-concept Phase 2a trial of SION-719, an important milestone for Sionna,\" said Mike Cloonan, President and Chief Executive Officer of Sionna. \"With both of our clinical stage NBD1 stabilizer programs on track for topline readouts this summer, we remain focused on advancing these first-in-class product candidat","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://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":["SOC","BK4218","BK4585","BK4588","CF","SION","BK4139","BK4093","BK4213","BK4181","PK"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634232653","title":"Erasca Reports First Quarter 2026 Business Updates and Financial Results","url":"https://stock-news.laohu8.com/highlight/detail?id=2634232653","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2634232653?lang=en_us&edition=fundamental","pubTime":"2026-05-12 04:01","pubTimestamp":1778529660,"startTime":"0","endTime":"0","summary":"Robust monotherapy efficacy and generally well-tolerated safety results observed during dose escalation for ERAS-0015 in both KRAS G12X NSCLC and PDAC reinforce best-in-class potential across RAS-targ","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2026/05/11/3292285/0/en/Erasca-Reports-First-Quarter-2026-Business-Updates-and-Financial-Results.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4539","IE0031619046.USD","BK4218","IE00B66KJ199.SGD","IE00B7SZL793.SGD","LU1559883803.SGD","BK4139","ERAS","DCO","LU0566484027.USD","BK4187","PK","IE00B19Z4B17.USD","BK4181"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634928323","title":"MBX Biosciences Provides Obesity Portfolio Update Including Initial Phase 1 Data for MBX 4291 Supporting Potential for Once-Monthly Dosing","url":"https://stock-news.laohu8.com/highlight/detail?id=2634928323","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2634928323?lang=en_us&edition=fundamental","pubTime":"2026-05-11 19:00","pubTimestamp":1778497200,"startTime":"0","endTime":"0","summary":"Preliminary blinded data from ongoing Phase 1 trial demonstrated mean weight loss of 7% (range 0-16%) at 8 weeks in first MAD Part B cohort (n=8, including 2 placebo) MBX 4291 generally well tolerated","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2026/05/11/3291731/0/en/MBX-Biosciences-Provides-Obesity-Portfolio-Update-Including-Initial-Phase-1-Data-for-MBX-4291-Supporting-Potential-for-Once-Monthly-Dosing.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4567","MTD","BK4533","LU2413666426.HKD","MBX","BK4585","LU2413666699.HKD","LU2211817866.USD","IE00BFXG0V08.USD","LU1093756325.SGD","BK4218","LU1721428933.USD","BK4181","IE00BYQQ9H92.USD","PBH","BK4588","BK4007","LU0347712357.USD","IE00B5TLWC47.USD","PK","BK4548","BK4121","LU1093756168.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634828842","title":"Press Release: Actuate Therapeutics Announces FDA Clearance of IND for Oral Elraglusib and Strategic Initiatives to Advance the Elraglusib Development Program","url":"https://stock-news.laohu8.com/highlight/detail?id=2634828842","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2634828842?lang=en_us&edition=fundamental","pubTime":"2026-05-11 19:00","pubTimestamp":1778497200,"startTime":"0","endTime":"0","summary":"-- Elraglusib oral tablet formulation to drive next-phase clinical. -- FDA cleared IND for Phase 1/2 study of oral elraglusib in advanced cancer. patients, with focus on metastatic melanoma, NSCLC, colorectal, and. pancreatic cancers with initiation planned for 2H 2026. To support this initiative, the Company recently received Investigational New Drug  clearance from FDA to conduct a Phase 1/2 study designed to demonstrate that a higher overall exposure to elraglusib can be achieved with the oral formulation compared to the IV formulation. The study will evaluate the safety and potential efficacy of the oral formulation as a monotherapy in solid tumor patients, including those with metastatic melanoma, NSCLC, colorectal, and pancreatic cancers, based on evidence of efficacy of the IV formulation in prior clinical studies and machine learning therapeutic target analyses.\"Advancing the elraglusib oral tablet is an important element to the success of our overall development strategy,\" sai","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","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":["ACTU","BK4548","PK","IE00B5TLWC47.USD","IE00BFXG0V08.USD","BK4121","BK4588","LABU","LU1093756168.USD","BK4218","LU2413666426.HKD","BK4567","LU2413666699.HKD","BK4139","IE00BYQQ9H92.USD","LU1721428933.USD","BK4533","IND","EMA","BK4081","BK4181","LU0347712357.USD","LU2211817866.USD","BK4585","LU1093756325.SGD","MTD"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":8,"pageCount":6,"totalSize":153,"code":"91000000","status":"200"}]}}