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Park Hotels & Resorts Inc.

9.98

-0.1700-1.67%

Volume:1.81M

Turnover:18.04M

Market Cap:2.01B

PE:9.88

High:10.20

Open:10.04

Low:9.90

Close:10.15

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Overview Company News Filings

Press Release: InflaRx Reports Full Year 2024 Results and Highlights Key Achievements and Expected Milestones

Press Release: Sionna Therapeutics Reports Fourth Quarter and Full Year 2024 Financial Results

Acumen Pharmaceuticals Announces Topline Results from Phase 1 Study of Subcutaneous Formulation of Sabirnetug in Healthy Volunteers

Park Hotels & Resorts Inc. Announces First Quarter 2025 Earnings Conference Call on May 5, 2025

Press Release: Protalix BioTherapeutics Reports Fiscal Year 2024 Financial and Business Results

Neurizon moves to lift FDA clinical hold on motor neurone drug

Scholar Rock Presents New Phase 3 SAPPHIRE Data at the 2025 Muscular Dystrophy Association Clinical & Scientific Conference

Race gets ethics nod for Phase I trial in solid tumour patients

Press Release: Rallybio Reports Fourth Quarter and Full Year 2024 Financial Results and Provides Business Updates

TransCode Therapeutics Announces Safety Review Committee Approval to Open Fourth Cohort in Phase I/II Clinical Trial

Press Release: Vigil Neuroscience Reports Fourth Quarter and Full Year 2024 Financial Results and Provides Recent Business Updates

Press Release: Ovid Therapeutics Reports Business Updates and Fourth Quarter and Full Year 2024 Financial Results

Design Therapeutics Highlights Progress Across Lead GeneTAC® Programs and Reports Fourth Quarter and Full Year 2024 Financial Results

CING: April Pre-NDA Meeting

Zacks Small Cap Research

Q32 Bio Presents Results from SIGNAL-AA Part A Clinical Trial Evaluating Bempikibart in Patients with Alopecia Areata at the 2025 American Academy of Dermatology Meeting

Oruka Therapeutics Announces Preclinical Data for ORKA-002 at the 2025 American Academy of Dermatology Annual Meeting

InflaRx Showcases Vilobelimab’s Role in Immuno-Dermatology at the 2025 AAD Annual Meeting

Agios Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) to Newly Appointed Chief Corporate Development & Strategy Officer

ARS Pharmaceuticals Announces FDA Approval of neffy® 1 mg (epinephrine nasal spray) for Type I Allergic Reactions, Including Anaphylaxis, in Pediatric Patients Weighing 15 to < 30 Kilograms

Zymeworks Provides Corporate Update and Reports Fourth Quarter and Full Year 2024 Financial Results

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In December 2024, InflaRx announced that the first patient had been dosed in its Phase 2a basket study with INF904 in CSU and HS. This is a multi-center, open-label study evaluating multiple INF904 dosing regimens over 4 weeks of treatment in a total of 75 patients . The goal of the trial is to generate additional safety and pharmacokinetic  data and to provide signs of clinical benefit. After the 4-week treatment period, patients will be follow","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://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":["LU0094547139.USD","IE000M9KFDE8.USD","LU2242652126.USD","BK4022","LU1868837136.USD","IE00BWXC8680.SGD","LU0323591593.USD","BK4567","BK4585","LU0640476718.USD","LU0098860793.USD","IE00B3T34201.USD","SG9999015341.SGD","LU1929549753.HKD","SG9999002232.USD","IE00BLSP4452.SGD","BK4559","LU0061475181.USD","LU1430594728.SGD","LU0234570918.USD","BK4588","LU1868837300.USD","ARDS","PK","R","LU0124676726.USD","LU2552382132.HKD","LU1868836757.USD","LU1585245621.USD","LU0096364046.USD","BK4181","LU0689626769.HKD","BK4218","BK4139","BK4201","LU0868494617.USD","LU2129689431.USD","LU0320765646.SGD","EC","BK4018","LU0234572021.USD","LU1914381329.SGD","LU1162221912.USD","SG9999014567.USD","SG9999002224.SGD","LU0237698245.USD","PG","IE00B1XK9C88.USD","IFRX"],"gpt_icon":0},{"id":"2520437381","title":"Press Release: Sionna Therapeutics Reports Fourth Quarter and Full Year 2024 Financial Results","url":"https://stock-news.laohu8.com/highlight/detail?id=2520437381","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520437381?lang=en_us&edition=fundamental","pubTime":"2025-03-20 19:00","pubTimestamp":1742468400,"startTime":"0","endTime":"0","summary":"Phase 1 MAD dosing completed for SION-451 and final MAD cohort of SION-719 planned; Interim data in healthy volunteers show potential to provide clinically meaningful benefit to CF patients. Topline data anticipated in first half of 2025. On track to initiate NBD1 Phase 2a proof-of-concept trial in combination with SOC in CF patients and combination MAD trials of an NBD1 stabilizer with a complementary modulator in healthy volunteers in the second half of 2025, with topline data for both anticipated in mid-2026. Completed upsized IPO with gross proceeds of approximately $219 million, extending runway into 2028","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4093","BK4218","BK4588","BK4213","BK4139","SOC","CF","SION","PK","BK4585","BK4181"],"gpt_icon":0},{"id":"2520185769","title":"Acumen Pharmaceuticals Announces Topline Results from Phase 1 Study of Subcutaneous Formulation of Sabirnetug in Healthy Volunteers","url":"https://stock-news.laohu8.com/highlight/detail?id=2520185769","media":"GlobeNewswire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520185769?lang=en_us&edition=fundamental","pubTime":"2025-03-19 20:00","pubTimestamp":1742385600,"startTime":"0","endTime":"0","summary":"Weekly subcutaneous administration of sabirnetug was well-tolerated in the Phase 1 study. Systemic exposure following subcutaneous administration supports further clinical development. Development of sabirnetug delivered subcutaneously has the potential for decreased treatment burden and increased patient convenience. Sabirnetug is the first humanized monoclonal antibody to clinically demonstrate selective target engagement of AβOs in patients with AD. The SC formulation of sabirnetug is co-formulated with Halozyme’s proprietary ENHANZE drug delivery technology  that enables large volume SC injection with increased dispersion and absorption of co-administered therapies. ENHANZE has been commercially validated as a component of nine approved therapies.Sabirnetug  is a humanized monoclonal antibody  discovered and developed based on its selectivity for soluble amyloid beta oligomers , which are a highly toxic and pathogenic form of Aβ, relative to Aβ monomers and amyloid plaques. Soluble","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/acumen-pharmaceuticals-announces-topline-results-120000503.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":["ABOS","PK","BK4139","BK4539","BK4181","BK4218"],"gpt_icon":0},{"id":"2520934430","title":"Park Hotels & Resorts Inc. Announces First Quarter 2025 Earnings Conference Call on May 5, 2025","url":"https://stock-news.laohu8.com/highlight/detail?id=2520934430","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520934430?lang=en_us&edition=fundamental","pubTime":"2025-03-19 04:15","pubTimestamp":1742328900,"startTime":"0","endTime":"0","summary":"TYSONS, Va., March 18, 2025----Park Hotels & Resorts Inc.   today announced that it will release its financial results for the first quarter 2025 before the stock market opens on Monday, May 5, 2025. Park will hold a conference call at 10:00 a.m. Eastern Time  that same morning to discuss its earnings results, current operational environment and business outlook.The conference call will be accessible by telephone and through the internet. Interested individuals are invited to participate by following these steps:. Telephone:Please dial  451-6152, or  389-0879 for international participants, and request Park Hotels & Resorts’ First Quarter 2025 Earnings Conference Call. It is recommended that participants dial 10 minutes ahead of the scheduled start time.","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/park-hotels-resorts-inc-announces-201500966.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":["PK"],"gpt_icon":0},{"id":"2520512546","title":"Press Release: Protalix BioTherapeutics Reports Fiscal Year 2024 Financial and Business Results","url":"https://stock-news.laohu8.com/highlight/detail?id=2520512546","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520512546?lang=en_us&edition=fundamental","pubTime":"2025-03-17 18:50","pubTimestamp":1742208600,"startTime":"0","endTime":"0","summary":"Company to host conference call and webcast today at 8:30 a.m. EDT. \"2024 was a record year in revenues from selling goods for Protalix, as we experienced increases in all three of our revenue streams, Chiesi, Pfizer and Brazil,\" said Dror Bashan, Protalix's President and Chief Executive Officer. \"We are pleased with the promising results from our first-in-human study of our gout candidate, PRX-115, in adult volunteers with elevated uric acid levels, and hope to build on this momentum with the goal of initiating a phase II clinical trial in patients with gout during the second half of 2025. At the same time, we continued to evaluate additional pipeline candidates, including PRX-119, for potential further development. Now that our debt is fully repaid and we no longer have outstanding warrants, our balance sheet is stronger and we are well-positioned to continue executing on our strategy through 2025 and beyond.\"","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":["LU0321505868.SGD","IE00B19Z3B42.SGD","BK4581","PK","LU0225771236.USD","PLX","LU0225284248.USD","LU0058720904.USD","LU0170899867.USD","SGXZ57979304.SGD","BK4599","LU1057294990.SGD","IE00B19Z3581.USD","LU1066053197.SGD","LU0306807586.USD","LU1883839398.USD","BK4110","LU1894683264.USD","LU0456855351.SGD","SG9999002232.USD","BK4585","LU1894683348.USD","BK4215","SG9999001176.SGD","BK4232","SG9999003800.SGD","LU0289739699.SGD","BK4218","BK4534","BK4592","MAA","SG9999002224.SGD","LU0868494617.USD","R","SG9999001176.USD","LU0306806265.USD","ACR","IE0002270589.USD","IE00BLSP4452.SGD","BK4139","BK4588","SG9999011175.SGD","BK4022","LU0234572021.USD","IE00BBT3K403.USD","LU0122379950.USD","LU1023059063.AUD","IE00BLSP4239.USD","SG9999013999.USD"],"gpt_icon":1},{"id":"2520550989","title":"Neurizon moves to lift FDA clinical hold on motor neurone drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2520550989","media":"Stockheads","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520550989?lang=en_us&edition=fundamental","pubTime":"2025-03-17 13:20","pubTimestamp":1742188832,"startTime":"0","endTime":"0","summary":"Neurizon submits formal request to US FDA for clarification on pharmacokinetic studies needed to lift hold on its IND application for NUZ-001. FDA expected to issue formal response to request within 60 days. Neurizon to proactively start pharmacokinetic studies required to generate additional animal exposure data","market":"us","thumbnail":"https://stockhead.com.au/wp-content/uploads/2025/03/image-1200x675-2025-03-17T121621.237-640x360.jpg","type":0,"news_type":0,"thumbnails":["https://stockhead.com.au/wp-content/uploads/2025/03/image-1200x675-2025-03-17T121621.237-640x360.jpg"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://stockhead.com.au/health/neurizon-moves-to-lift-fda-clinical-hold-on-motor-neurone-drug/","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":"stockheads_stock","symbols":["BK4181","PK","BK4218"],"gpt_icon":0},{"id":"2520965587","title":"Scholar Rock Presents New Phase 3 SAPPHIRE Data at the 2025 Muscular Dystrophy Association Clinical & Scientific Conference","url":"https://stock-news.laohu8.com/highlight/detail?id=2520965587","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520965587?lang=en_us&edition=fundamental","pubTime":"2025-03-17 07:00","pubTimestamp":1742166000,"startTime":"0","endTime":"0","summary":"Primary endpoint showed clinically meaningful improvement in patients with SMA receiving apitegromab as measured by gold standard Hammersmith Functional Motor Scale Expanded  versus placebo , with consistent outcomes across all major sub-groups including age, SMN-targeted background therapy, and age at initiation of SMN-targeted therapy. Pre-specified secondary endpoint showed that 30.4% of patients receiving apitegromab had ≥ 3-point improvement in HFMSE versus 12.5% of patients on placebo , despite all study patients receiving ongoing SMN-targeted background therapy. During this week’s 2025 MDA Conference, the SAPPHIRE trial presentations highlight new data including secondary endpoint analyses. In addition to achieving the SAPPHIRE trial’s primary endpoint as previously announced in October 2024, apitegromab demonstrated a clinically meaningful and consistent benefit in motor function across pre-specified patient subgroups . Efficacy was also consistent across patient outcome measur","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/scholar-rock-presents-phase-3-230000179.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":["BK4213","PK","BK4218","MDA","LU1169590202.USD","BK4139","SRRK","BK4023","BK4181","SOC","LU1169589451.USD","PD"],"gpt_icon":0},{"id":"2519419548","title":"Race gets ethics nod for Phase I trial in solid tumour patients","url":"https://stock-news.laohu8.com/highlight/detail?id=2519419548","media":"Stockheads","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2519419548?lang=en_us&edition=fundamental","pubTime":"2025-03-14 14:06","pubTimestamp":1741932418,"startTime":"0","endTime":"0","summary":"Bellberry Human Research Ethics Committee approves a Phase I trial of RC220 bisantrene in adult solid tumour patients. Lead clinical site Southside Cancer Care Centre will start enrolling patients this month pending institutional approval and site activation. Up to nine other sites to follow with ethics approval sought in Hong Kong and South Korea","market":"nz","thumbnail":"https://stockhead.com.au/wp-content/uploads/2025/03/image-1200x765-3-640x408.jpg","type":0,"news_type":0,"thumbnails":["https://stockhead.com.au/wp-content/uploads/2025/03/image-1200x765-3-640x408.jpg"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://stockhead.com.au/health/race-gets-ethics-nod-for-phase-i-trial-in-solid-tumour-patients/","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":"stockheads_stock","symbols":["PK","BK4181","BK4218"],"gpt_icon":0},{"id":"2519944835","title":"Press Release: Rallybio Reports Fourth Quarter and Full Year 2024 Financial Results and Provides Business Updates","url":"https://stock-news.laohu8.com/highlight/detail?id=2519944835","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2519944835?lang=en_us&edition=fundamental","pubTime":"2025-03-13 20:00","pubTimestamp":1741867200,"startTime":"0","endTime":"0","summary":"-- Key Data Readouts from Sentinel Participant in RLYB212 Phase 2 Clinical Trial Expected in 2Q 2025 and 3Q 2025 --. -- Initiation of RLYB116 Confirmatory PK/PD Study Expected in 2Q 2025, with Data Anticipated in 2H 2025 --. -- $65.5 Million in Cash, Cash Equivalents, and Marketable Securities as of December 31, 2024 Provides Runway into 2H 2026 --. Rallybio Corporation , a clinical-stage biotechnology company translating scientific advances into transformative therapies for patients with devastating rare diseases, today reported financial results for the fourth quarter and full year ended December 31, 2024, and provided an update on recent company developments.-- In February 2025, Rallybio announced that the sentinel participant was. dosed in the Phase 2 trial investigating RLYB212 in pregnant women at. higher risk for HPA-1a alloimmunization and fetal and neonatal alloimmune. second trimester are expected in the second quarter of 2025, with PK and. safety data at the time of delivery","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4218","BK4194","BK4089","BK4109","ASH","BK4223","BK4139","TSAT","HPP","RLYB","PK","BK4539","BK4181","LU2463526074.USD"],"gpt_icon":0},{"id":"2519558835","title":"TransCode Therapeutics Announces Safety Review Committee Approval to Open Fourth Cohort in Phase I/II Clinical Trial","url":"https://stock-news.laohu8.com/highlight/detail?id=2519558835","media":"PR Newswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2519558835?lang=en_us&edition=fundamental","pubTime":"2025-03-13 19:47","pubTimestamp":1741866420,"startTime":"0","endTime":"0","summary":"Clinical trial Safety Review Committee  approved opening of Cohort 4 based on favorable safety data from the three patients comprising Cohort 3. No significant safety or dose limiting toxicities reported in Cohorts 1, 2, or 3. Patients currently being evaluated for Cohort 4 eligibility. \"SRC approval to open the fourth cohort and expand enrollment in Cohort 3 is an important advancement for the clinical trial. It will provide an opportunity to obtain additional safety and PK/PD data, inform the dose expansion stage of the clinical trial and may allow us to obtain initial evidence of clinical activity\" commented Sue Duggan, TransCode's Senior Vice President of Operations. Duggan added, \"Enrollment into the study continues based on the cumulative safety data review. Eligible subjects may now be screened and scheduled in Cohort 4 for treatment with the next dose level of TTX-MC138","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"yahoofinance","url":"https://finance.yahoo.com/news/transcode-therapeutics-announces-safety-review-114700704.html","rn_cache_url":null,"customStyle":"img, svg { display: none !important; }","selectors":"article","filters":"","directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/transcode-therapeutics-announces-safety-review-114700704.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":["BK4139","LU1169590202.USD","PK","BK4181","RNAZ","SRC","BK4231","BK4539","BK4218","PD","LENZ","LU1169589451.USD","BK4080","BK4023"],"gpt_icon":0},{"id":"2519887161","title":"Press Release: Vigil Neuroscience Reports Fourth Quarter and Full Year 2024 Financial Results and Provides Recent Business Updates","url":"https://stock-news.laohu8.com/highlight/detail?id=2519887161","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2519887161?lang=en_us&edition=fundamental","pubTime":"2025-03-13 19:00","pubTimestamp":1741863600,"startTime":"0","endTime":"0","summary":"Vigil Neuroscience Reports Fourth Quarter and Full Year 2024 Financial Results and Provides Recent Business Updates. -- Announced positive data from Phase 1 clinical trial evaluating VG-3927 for potential treatment of Alzheimer's Disease ; plans to initiate Phase 2 clinical trial in Q3 2025 --. -- On track to report final analysis from IGNITE Phase 2 clinical trial evaluating iluzanebart in ALSP in Q2 2025 --. WATERTOWN, Mass., March 13, 2025  -- Vigil Neuroscience, Inc. , a clinical-stage biotechnology company committed to harnessing the power of microglia for the treatment of neurodegenerative diseases, today announced financial results for the fourth quarter and full year ended December 31, 2024, and provided updates on recent progress.Final analysis from IGNITE Phase 2 clinical trial planned for second quarter of 2025:. -- The Company plans to report the final analysis from the IGNITE Phase 2. clinical trial, including all patients at 12 months dosed with either 20. iluzanebart in ","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":["BK4604","BK4555","BK4139","PD","BK4023","PK","BK4213","LU1169589451.USD","03160","VIGL","VG","LU1169590202.USD","BK4585","CSF","TM","BK4181","BK4218","BK4588","BK4099"],"gpt_icon":0},{"id":"2518748696","title":"Press Release: Ovid Therapeutics Reports Business Updates and Fourth Quarter and Full Year 2024 Financial Results","url":"https://stock-news.laohu8.com/highlight/detail?id=2518748696","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518748696?lang=en_us&edition=fundamental","pubTime":"2025-03-11 20:00","pubTimestamp":1741694400,"startTime":"0","endTime":"0","summary":"-- Stelios Papadopolous, Ph.D., a pioneering leader in biotech, appointed to. Board of Directors; two industry veterans joined management team as Ovid. prepares to take OV329 into patient trials and move its first KCC2 direct. -- Topline results from Phase 1 study of OV329 expected in Q3 2025, which. will include biomarkers that measure clinical effect and target. -- OV350, Ovid's first program in its KCC2 direct activator library,Ovid expects its cash runway to support operations and clinical development programs into the second half of 2026, during which time multiple pipeline and regulatory milestones are anticipated. These anticipated milestones include: results for OV329 biomarker and safety data ; initiation of a Phase 2a patient study for OV329 in drug resistant epilepsies ; results from a first-in-human safety and exploratory biomarker study with OV350, our first KCC2 direct activator ; and initiation of human trials for the first oral KCC2 direct activator, OV4071 . 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As we move down the home stretch towards the FDA submission, Cingulate has a pre-new drug application  meeting scheduled for early April and anticipates filing its NDA with the agency by mid-2025. We also expect to see further safety data from the consolidated Phase III studies at an upcoming but as yet unidentified scientific conference.The pathway forward for FDA submission includes several parallel efforts which include updating stability data on 2024 batches of CTx-1301, completing the analysis of the fast fed study and attendance at the pre-NDA meeting with the FDA in early April. Notes from the meeting are expected about a month later, which will provide final details required for completing the NDA. NDA submission is expected by mid-2025. We anticipate a 10-to-12-month turnaround time by the agenc","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/cing-april-pre-nda-meeting-094000188.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":["API","BK4023","BK4181","PK","CINGW","CMAX","BK4218","BK4535","BK4007","BK4196","BK4551","BK4503","CING"],"gpt_icon":0},{"id":"2518440883","title":"Q32 Bio Presents Results from SIGNAL-AA Part A Clinical Trial Evaluating Bempikibart in Patients with Alopecia Areata at the 2025 American Academy of Dermatology Meeting","url":"https://stock-news.laohu8.com/highlight/detail?id=2518440883","media":"PR Newswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518440883?lang=en_us&edition=fundamental","pubTime":"2025-03-09 00:00","pubTimestamp":1741449600,"startTime":"0","endTime":"0","summary":"-- Results presented in AAD late-breaker demonstrate bempikibart's encouraging improvement on SALT reduction at week 24 and continued effects after dosing cessation in patients with severe and very severe alopecia areata  --. -- Durable, ongoing responses in multiple patients through week 36 follow-up period and beyond to week 55, despite only 24 weeks of dosing, suggestive of potential for remittive effect; multiple inbound patient requests to re-initiate dosing --. -- Bempikibart development program remains on track with open-label extension study to initiate in 1H'25; SIGNAL-AA Part B remains on track for initiation of dosing in 1H'25, with topline data expected in 1H'26 --. WALTHAM, Mass., March 8, 2025 /PRNewswire/ --Q32 Bio Inc.  , a clinical stage biotechnology company focused on developing biologic therapeutics to restore immune homeostasis, today announced additional results from Part A of its SIGNAL-AA Phase 2a clinical trial of bempikibart in patients with alopecia areata  a","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"yahoofinance","url":"https://finance.yahoo.com/news/q32-bio-presents-results-signal-160000777.html","rn_cache_url":null,"customStyle":"img, svg { display: none !important; }","selectors":"article","filters":"","directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/q32-bio-presents-results-signal-160000777.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":["BK4153","BK4139","BK4181","BK4117","AA","BK4218","AFG","BK4585","BK4107","BK4588","QTTB","PK"],"gpt_icon":0},{"id":"2517276438","title":"Oruka Therapeutics Announces Preclinical Data for ORKA-002 at the 2025 American Academy of Dermatology Annual Meeting","url":"https://stock-news.laohu8.com/highlight/detail?id=2517276438","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517276438?lang=en_us&edition=fundamental","pubTime":"2025-03-07 21:30","pubTimestamp":1741354200,"startTime":"0","endTime":"0","summary":"Half-life in non-human primates (NHP) of more than 30 days, over three times longer than bimekizumab and expected to support a dose interval of two to three times per year Equivalent potency to bimeki","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/2025/03/07/3038935/0/en/Oruka-Therapeutics-Announces-Preclinical-Data-for-ORKA-002-at-the-2025-American-Academy-of-Dermatology-Annual-Meeting.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":["PK","BK4218","AFG","ORKA","BK4139","BK4117","BK4181","BK4107"],"gpt_icon":0},{"id":"2517480505","title":"InflaRx Showcases Vilobelimab’s Role in Immuno-Dermatology at the 2025 AAD Annual Meeting","url":"https://stock-news.laohu8.com/highlight/detail?id=2517480505","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517480505?lang=en_us&edition=fundamental","pubTime":"2025-03-07 21:00","pubTimestamp":1741352400,"startTime":"0","endTime":"0","summary":"JENA, Germany, March  07, 2025  (GLOBE NEWSWIRE) -- InflaRxN.V.(Nasdaq:IFRX), a biopharmaceutical company pioneering anti-inflammatory therapeutics targeting the complement system, today announced the","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/2025/03/07/3038913/0/en/InflaRx-Showcases-Vilobelimab-s-Role-in-Immuno-Dermatology-at-the-2025-AAD-Annual-Meeting.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":["BK4139","LU2129689431.USD","BK4568","LU2552382215.SGD","PG","SG9999015358.SGD","IE00B3T34201.USD","IE00BWXC8680.SGD","IE00BBT3K403.USD","LU0094547139.USD","LU1868837136.USD","SG9999014575.USD","BK4181","BK4533","BK4558","ARDS","BK4504","LU1585245621.USD","LU1162221912.USD","LU1868836914.USD","LU1868837300.USD","SG9999001440.SGD","SG9999002224.SGD","SG9999014567.USD","LU1066053197.SGD","USA","BK4559","LU2129689514.USD","BK4581","SG9999014542.SGD","SG9999015341.SGD","LU0689626769.HKD","BK4535","LU1066051498.USD","LU0061475181.USD","IE00BLSP4239.USD","LU1169589451.USD","LU0868494617.USD","LU1868836591.USD","LU0234570918.USD","LU1430594728.SGD","BK4018","LU1929549753.HKD","BK4567","LU0234572021.USD","PK","BK4534","SG9999002232.USD","PD","BNTX"],"gpt_icon":0},{"id":"2517978319","title":"Agios Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) to Newly Appointed Chief Corporate Development & Strategy Officer","url":"https://stock-news.laohu8.com/highlight/detail?id=2517978319","media":"GlobeNewswire","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517978319?lang=en_us&edition=fundamental","pubTime":"2025-03-06 06:52","pubTimestamp":1741215120,"startTime":"0","endTime":"0","summary":"CAMBRIDGE, Mass., March  05, 2025  (GLOBE NEWSWIRE) -- Agios Pharmaceuticals, Inc. 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