Actuate Therapeutics to Be Added to Russell 2000 Index
Actuate Therapeutics to Be Added to Russell 2000 Index
CHICAGO and FORT WORTH, Texas, Nov. 26, 2024 (GLOBE NEWSWIRE) -- Actuate Therapeutics, Inc. (NASDAQ: ACTU) ("Actuate" or the "Company"), a clinical-stage biopharmaceutical company focused on developing therapies for the treatment of high-impact, difficult-to-treat cancers announced today that the Company will be added to the Russell 2000 Index as part of the planned fourth quarter IPO additions effective after the U.S market opens on December 23, 2024.
芝加哥和德克薩斯州沃斯堡,2024年11月26日(環球新聞) -- Actuate Therapeutics, Inc.(納斯達克:ACTU)("Actuate"或"公司"),是一家臨床階段的生物製藥公司,專注於開發用於治療高影響、難治性癌症的療法,今天宣佈公司將作爲計劃中的第四季度已上市新股添加到羅素2000指數,該變動將在2024年12月23日美國市場開盤後生效。
The Russell 2000 Index measures the performance of the small-cap segment of the US equity market. The Russell 2000 Index is a subset of the Russell 3000 Index representing approximately 10% of the total market capitalization of that index. It includes approximately 2,000 of the smallest securities based on a combination of their market cap and current index membership. Initial public offerings (IPOs) are added to the Russell US indexes on a quarterly basis. For more information on the Russell 2000 Index and the Preliminary List of IPO Additions: Russell US Index IPO additions and reports | LSEG
羅素2000指數衡量美國股市小盤股市場的表現。羅素2000指數是羅素3000指數的一個子集,代表該指數總市值的約10%。它包括約2000個最小的證券,這些證券是基於其市值和當前指數成員資格的組合。已上市新股(IPOs)每季度添加到羅素美國指數。有關羅素2000指數和已上市新股添加初步名單的更多信息:羅素美國指數已上市新股添加和報告 | LSEG
About Actuate Therapeutics, Inc.
關於Actuate Therapeutics,Inc。
Actuate is a clinical-stage biopharmaceutical company focused on developing therapies for the treatment of high-impact, difficult-to-treat cancers. Actuate's lead investigational drug product, elraglusib (a novel GSK-3β inhibitor), targets molecular pathways in cancer that are involved in promoting tumor growth and resistance to conventional cancer drugs such as chemotherapy including several DDR pathways. Elraglusib is designed to act as a mediator of anti-tumor immunity through the inhibition of NF-kB and regulates multiple immune checkpoints and immune cell function. For additional information, please visit the Company's website at .
Actuate 是一家專注於開發治療高影響力、難以治療的癌症的臨床階段生物製藥公司。Actuate 的首個研發藥物產品 elraglusib(一種新型 GSk-3β 抑制劑)針對癌症中涉及促進腫瘤生長和抗藥性的分子途徑,包括幾種 DNA 損傷應答 (DDR) 途徑。Elraglusib 被設計爲通過抑制 NF-kb,調節多重免疫檢查點和免疫細胞功能,以充當抗腫瘤免疫的中介物。有關詳情,請訪問該公司網站。
Forward-Looking Statements
前瞻性聲明
This press release contains forward-looking statements about us, including our clinical trials, development plans, industry, and our planned addition of the Russell 2000 Index. The words "anticipate," "believe," "continue," "could," "estimate," "expect," "intend," "may," "might," "ongoing," "plan," "potential," "predict," "project," "should," "target," "will," "would," or the negative of these terms or other comparable terminology are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. All statements, other than statements related to present facts or current conditions or of historical facts, contained in this press release are forward-looking statements. Accordingly, these statements involve estimates, assumptions, substantial risks and uncertainties which could cause actual results to differ materially from those expressed in them, including but not limited to the potential benefits of and continued inclusion of the Company in the Russell 2000 Index, that clinical and preclinical drug development involves a lengthy and expensive process with uncertain timelines and outcomes, results of prior preclinical studies and early clinical trials are not necessarily predictive of future results, and elraglusib may not achieve favorable results in clinical trials or preclinical studies or receive regulatory approval on a timely basis, if at all; that we may not successfully enroll additional patients or establish or advance plans for further development; that elraglusib could be associated with side effects, adverse events or other properties or safety risks, which could delay or preclude regulatory approval, cause us to suspend or discontinue clinical trials or result in other negative consequences; our reliance on third parties to conduct our non-clinical studies and our clinical trials; our reliance on third-party licensors and ability to preserve and protect our intellectual property rights; that we face significant competition from other biotechnology and pharmaceutical companies; and our ability to fund development activities. In addition, any forward-looking statements are qualified in their entirety by reference to the factors discussed under the heading "Item 1A. Risk Factors" in our Quarterly Report on Form 10-Q for the quarter ended June 30, 2024 filed with the SEC on November 13, 2024 and other filings with the SEC. Because the risk factors referred to above could cause actual results or outcomes to differ materially from those expressed in any forward-looking statements made by us or on our behalf, you should not place undue reliance on any forward-looking statements. Further, any forward-looking statement speaks only as of the date on which it is made. New factors emerge from time to time, and it is not possible for us to predict which factors will arise. In addition, we cannot assess the impact of each factor on our business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements. Unless legally required, we do not undertake any obligation to release publicly any revisions to such forward-looking statements to reflect events or circumstances after the date of this press release or to reflect the occurrence of unanticipated events.
本新聞稿包含關於我們的前瞻性聲明,包括我們的臨床試驗、開發計劃、行業以及我們計劃將納入羅素2000指數。"預期"、"相信"、"繼續"、"可能"、"估計"、"期望"、"打算"、"可能"、"會"、"進行中"、"計劃"、"潛在"、"預測"、"項目"、"應該"、"目標"、"將"、"會"或這些術語的否定形式或其他可比術語旨在識別前瞻性聲明,儘管並非所有前瞻性聲明都包含這些識別詞。除與當前事實或條件或歷史事實相關的聲明外,本新聞稿中所有聲明均爲前瞻性聲明。因此,這些聲明涉及估計、假設、重大風險和不確定性,這可能導致實際結果與其所表達的結果存在重大差異,包括但不限於公司在羅素2000指數中的持續納入的潛在利益,臨床和臨床前藥物開發涉及一個漫長且昂貴的過程,時間和結果不確定,先前臨床前研究和早期臨床試驗的結果不一定能預測未來的結果,elraglusib可能無法在臨床試驗或臨床前研究中獲得良好的結果,或不能及時獲得監管批准(如果能獲得的話);我們可能無法成功招募額外的患者或建立或推進進一步發展的計劃;elraglusib可能與副作用、不良事件或其他特性或安全風險相關,這可能延遲或阻止監管批准,導致我們暫停或終止臨床試驗或導致其他負面後果;我們依賴第三方進行非臨床研究和臨床試驗;我們依賴第三方許可方並有能力維護和保護我們的知識產權;我們面臨來自其他生物技術和藥品公司的顯著競爭;以及我們資助開發活動的能力。此外,任何前瞻性聲明都完全以我們在2024年6月30日結束的季度向SEC提交的10-Q表格的"第1A項。風險因素"標題下討論的因素爲依據進行限定,並且其他在SEC的提交中討論的因素。因爲上述風險因素可能導致實際結果或結果與我們或代表我們所做的任何前瞻性聲明中表達的結果存在重大差異,因此您不應對任何前瞻性聲明過度依賴。此外,任何前瞻性聲明僅在做出聲明的日期有效。新因素會不時出現,我們無法預測哪些因素會出現。此外,我們無法評估每個因素對我們業務的影響,或任何因素或因素組合可能導致實際結果與任何前瞻性聲明中包含的結果存在重大差異的程度。除非法律規定要求,否則我們不承擔公開發布對這些前瞻性聲明的任何修訂義務,以反映本新聞稿日期之後的事件或情況,或反映意外事件的發生。
Investor Contact
投資者聯繫方式
Mike Moyer
邁克·莫迪爾
Managing Director
常務董事
LifeSci Advisors, LLC
LifeSci Advisors, LLC
mmoyer@lifesciadvisors.com
mmoyer@lifesciadvisors.com
譯文內容由第三人軟體翻譯。