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TRAWS PHARMA

1.99

-0.0052-0.26%

Volume:2.92K

Turnover:5.82K

Market Cap:15.94M

PE:-1.10

High:1.99

Open:1.99

Low:1.99

Close:2.00

52wk High:3.27

52wk Low:0.9700

Shares:7.99M

Float Shares:5.93M

Volume Ratio:0.40

T/O Rate:0.05%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-1.8200

EPS(LYR):-35.2126

ROE:-1059.63%

ROA:-92.29%

PB:3.51

PE(LYR):-0.06

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News

BUZZ-Traws Pharma falls after FDA puts flu drug application on clinical hold

BRIEF-Traws Pharma Completes Analysis Of Ratutrelvir Clinical Study In Paxlovid®-Eligible And Ineligible Covid-19 Patients

Traws Pharma reports Phase 2 ratutrelvir study results versus Paxlovid in COVID-19 patients

Traws Pharma Completes Analysis of Ratutrelvir Clinical Study in Paxlovid®-Eligible and Ineligible Covid-19 Patients and Provides Updates for Additional Indication for Tivoxavir Marboxil as a Prophylactic Treatment for Seasonal Influenza

THOMSON REUTERS

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Pharma falls after FDA puts flu drug application on clinical hold","url":"https://stock-news.laohu8.com/highlight/detail?id=2612400625","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2612400625?lang=en_us&edition=fundamental","pubTime":"2026-02-19 21:17","pubTimestamp":1771507073,"startTime":"0","endTime":"0","summary":"BUZZ-Traws Pharma falls after FDA puts flu drug application on clinical hold** Shares of Traws Pharma TRAW.O down 20.81% at $1.58 premarket** Co says the U.S. FDA placed on clinical hold its investigational new drug application for tivoxavir marboxil, a single oral tablet for prevention of seasonal influenza** Adds that FDA flagged concerns \"with the mutagenicity data package\" for drug in application** Also says it filed the application to allow the government's biomedical research unit to fully review its bid for inclusion in the strategic stockpile for avianflu treatment** Clinical hold does not directly impact ongoing and planned studies outside of the United States; working to mitigate issue in clinical development plan - TRAW  ** TRAW shares up 74.3% YTD       ","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260219:nL4N3ZF0XW:1","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":null,"symbols":["BK4007","TRAW"],"gpt_icon":0},{"id":"2612140749","title":"BRIEF-Traws Pharma Completes Analysis Of Ratutrelvir Clinical Study In Paxlovid®-Eligible And Ineligible Covid-19 Patients","url":"https://stock-news.laohu8.com/highlight/detail?id=2612140749","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2612140749?lang=en_us&edition=fundamental","pubTime":"2026-02-19 20:58","pubTimestamp":1771505921,"startTime":"0","endTime":"0","summary":"BRIEF-Traws Pharma Completes Analysis Of Ratutrelvir Clinical Study In Paxlovid-Eligible And Ineligible Covid-19 Patients Feb 19 (Reuters) - Traws Pharma Inc TRAW.O:TRAWS PHARMA COMPLETES ANALYSIS OF 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clinical analysis from a 90-patient, open-label Phase 2 study evaluating ratutrelvir, an investigational oral ritonavir-free Mpro/3CL protease inhibitor, versus PAXLOVID in mild-to-moderate COVID-19 patients, including a separate single-arm cohort of PAXLOVID-ineligible patients. The company said the analysis found fewer treatment-related adverse events and no viral rebound events in ratutrelvir-treated patients, with equivalent time to sustained symptom resolution versus PAXLOVID; in PAXLOVID-ineligible patients, it reported a shorter time to symptom resolution compared with PAXLOVID. The company also provided preclinical and development updates on tivoxavir marboxil tablets for once-monthly influenza prophylaxis, including plans for a PK study under an open IND in Australia and preparations for a human influenza prophylaxis challenge study in the UK. 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