CervoMed Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
CervoMed Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
BOSTON, Dec. 12, 2024 (GLOBE NEWSWIRE) -- CervoMed Inc. (NASDAQ: CRVO) (the "Company"), a clinical stage company focused on developing treatments for age-related neurologic disorders, today announced that it has granted equity awards as a material inducement to the employment of two new employees.
波士頓,2024年12月12日(GLOBE NEWSWIRE)——專注於開發年齡相關神經系統疾病治療方法的臨床階段公司CervoMed Inc.(納斯達克股票代碼:CRVO)(「公司」)今天宣佈,它已授予股權獎勵,以此作爲僱用兩名新員工的實質性激勵。
On December 6, 2024, the Company granted options to purchase an aggregate of 14,753 shares of common stock to two new employees. Each option has an exercise price of $11.91, the closing price of the Company's common stock on the grant date, and each will vest in 36 equal installments on the last day of each month over a three-year period, subject to the employee's continued employment with the Company on each such date. The awards were approved by the Compensation Committee of the Company's Board of Directors as an inducement material to each new employee entering into employment with the Company in accordance with Nasdaq Listing Rule 5635(c)(4).
2024年12月6日,公司向兩名新員工授予了購買總計14,753股普通股的期權。每種期權的行使價爲11.91美元,即授予日公司普通股的收盤價,每份期權將在三年內在每個月的最後一天分36次等額分期歸屬,前提是員工在每個此類日期繼續在公司工作。根據納斯達克上市規則5635(c)(4),這些獎勵已獲得公司董事會薪酬委員會的批准,作爲激勵每位新員工在公司工作的激勵材料。
About CervoMed
CervoMed Inc. is a clinical-stage company focused on developing treatments for age-related neurologic disorders. The Company is currently developing neflamapimod, an investigational, orally administered small molecule brain penetrant designed to inhibit p38 mitogen-activated protein kinase alpha. Neflamapimod has the potential to treat synaptic dysfunction, the reversible aspect of the underlying neurodegenerative processes that causes disease in certain other major neurological disorders.
關於 CervoMed
CervoMed Inc. 是一家臨床階段的公司,專注於開發與年齡相關的神經系統疾病的治療方法。該公司目前正在開發奈弗拉匹莫德,這是一種在研的口服小分子腦穿透劑,旨在抑制p38絲裂原活化蛋白激酶α型。奈弗拉匹莫德有可能治療突觸功能障礙,突觸功能障礙是導致某些其他主要神經系統疾病疾病疾病疾病的潛在神經退行過程的可逆方面。
Forward-Looking Statements
This press release includes express and implied forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, regarding the intentions, plans, beliefs, expectations or forecasts for the future of the Company, including, but not limited to, the therapeutic potential of neflamapimod. Terms such as "believes," "estimates," "anticipates," "expects," "plans," "aims," "seeks," "intends," "may," "might," "could," "might," "will," "should," "approximately," "potential," "target," "project," "contemplate," "predict," "forecast," "continue," or other words that convey uncertainty of future events or outcomes (including the negative of these terms) may identify these forward-looking statements. Although there is believed to be reasonable basis for each forward-looking statement contained herein, forward-looking statements by their nature involve risks and uncertainties, known and unknown, many of which are beyond the Company's control and, as a result, actual results could differ materially from those expressed or implied in any forward-looking statement. Particular risks and uncertainties include, among other things, those related to: the Company's available cash resources and the availability of additional funds on acceptable terms; the results of the Company's clinical trials, including RewinD-LB; the likelihood and timing of any regulatory approval of neflamapimod or the nature of any feedback the Company may receive from the U.S. Food and Drug Administration; the ability to implement business plans, forecasts, and other expectations in the future; general economic, political, business, industry, and market conditions, inflationary pressures, and geopolitical conflicts; and the other factors discussed under the heading "Risk Factors" in the Company's Annual Report on Form 10-K for the year ended December 31, 2023 filed with the U.S. Securities and Exchange Commission (SEC) on March 29, 2024, and other filings that the Company may file from time to time with the SEC. Any forward-looking statements in this press release speak only as of the date hereof (or such earlier date as may be identified). The Company does not undertake any obligation to update such forward-looking statements to reflect events or circumstances after the date of this press release, except to the extent required by law.
前瞻性陳述
本新聞稿包括經修訂的1995年《私人證券訴訟改革法》所指的明示和暗示的前瞻性陳述,內容涉及公司未來的意圖、計劃、信念、預期或預測,包括但不限於奈弗拉馬莫德的治療潛力。諸如 「相信」、「估計」、「預期」、「預期」、「計劃」、「目標」、「尋求」、「打算」、「可能」、「可能」、「可能」、「將」、「應該」、「大約」、「潛在」、「目標」、「項目」、「考慮」、「預測」、「繼續」 等術語表達未來事件或結果不確定性的詞語(包括這些術語的負面內容)可以識別這些前瞻性陳述。儘管據信此處包含的每項前瞻性陳述都有合理的依據,但就其性質而言,前瞻性陳述涉及已知和未知的風險和不確定性,其中許多風險和不確定性是公司無法控制的,因此,實際結果可能與任何前瞻性陳述中表達或暗示的結果存在重大差異。除其他外,特定的風險和不確定性包括與以下方面相關的風險和不確定性:公司的可用現金資源和可接受條件的額外資金的可用性;公司臨床試驗的結果,包括Rewind-LB;監管部門批准奈弗拉馬莫德的可能性和時機或公司可能從美國食品藥品監督管理局收到的任何反饋的性質;未來實施業務計劃、預測和其他預期的能力;概述經濟、政治、商業、工業和市場狀況、通貨膨脹壓力和地緣政治衝突;以及公司於2024年3月29日向美國證券交易委員會(SEC)提交的截至2023年12月31日止年度的10-k表年度報告以及公司可能不時向美國證券交易委員會(SEC)提交的其他文件中,在 「風險因素」 標題下討論的其他因素。本新聞稿中的任何前瞻性陳述僅代表截至本新聞稿發佈之日(或可能確定的較早日期)。除非法律要求,否則公司不承擔任何義務更新此類前瞻性陳述以反映本新聞稿發佈之日之後的事件或情況。
Investor Contact:
PJ Kelleher
LifeSci Advisors
Investors@cervomed.com
617-430-7579
投資者聯繫方式:
PJ Kelleher
LifeSCI 顧問
Investors@cervomed.com
617-430-7579