Immunic, Inc. to Participate in Investor Conference in December
Immunic, Inc. to Participate in Investor Conference in December
NEW YORK, Nov. 26, 2024 /PRNewswire/ -- Immunic, Inc. (Nasdaq: IMUX), a biotechnology company developing a clinical pipeline of orally administered, small molecule therapies for chronic inflammatory and autoimmune diseases, today announced that Daniel Vitt, Ph.D., Chief Executive Officer of Immunic, will participate in a fireside chat on Thursday, December 5, 2024, at 11:30 am ET, during the Piper Sandler 36th Annual Healthcare Conference, taking place December 3-5, 2024, in New York.
紐約,2024年11月26日 /PRNewswire/ -- Immunic, Inc.(納斯達克:IMUX)是一家開發口服小分子療法以治療慢性炎症和自身免疫疾病的生物技術公司,今天宣佈首席執行官Daniel Vitt博士將參加2024年12月5日東部時間11:30的爐邊對話,活動將在2024年12月3日至5日的派傑投資第36屆年度醫療會議上進行,地點在紐約。
Dr. Vitt, Glenn Whaley, Chief Financial Officer, and Jessica Breu, Vice President Investor Relations and Communications, will also participate in one-on-one investor meetings at the conference. To schedule a meeting, please contact your Piper Sandler representative or Jessica Breu at: [email protected].
Vitt博士、首席財務官Glenn Whaley和投資者關係及通信副總裁Jessica Breu也將參加會議上的一對一投資者會議。如需安排會議,請聯繫您的派傑投資代表或Jessica Breu,郵箱:[email protected]。
A webcast of the event will be available on the "Events and Presentations" section of Immunic's website at: . An archived replay will be available on the company's website for a period of 90 days after the conference.
活動的網絡直播將可在Immunic網站的「活動和演示」部分找到。會議結束後,公司網站上將提供90天的存檔回放。
About Immunic, Inc.
Immunic, Inc. (Nasdaq: IMUX) is a biotechnology company developing a clinical pipeline of orally administered, small molecule therapies for chronic inflammatory and autoimmune diseases. The company's lead development program, vidofludimus calcium (IMU-838), is currently in phase 3 and phase 2 clinical trials for the treatment of relapsing and progressive multiple sclerosis, respectively, and has shown therapeutic activity in phase 2 clinical trials in patients suffering from relapsing-remitting multiple sclerosis, progressive multiple sclerosis and moderate-to-severe ulcerative colitis. Vidofludimus calcium combines neuroprotective effects, through its mechanism as a first-in-class nuclear receptor related 1 (Nurr1) activator, with additional anti-inflammatory and anti-viral effects, by selectively inhibiting the enzyme dihydroorotate dehydrogenase (DHODH). IMU-856, which targets the protein Sirtuin 6 (SIRT6), is intended to restore intestinal barrier function and regenerate bowel epithelium, which could potentially be applicable in numerous gastrointestinal diseases, such as celiac disease, for which it is currently in preparations for a phase 2 clinical trial. IMU-381, which currently is in preclinical testing, is a next generation molecule being developed to specifically address the needs of gastrointestinal diseases. For further information, please visit: .
關於IMMUNIC, Inc.
Immunic, Inc. (納斯達克: IMUX) 是一家生物技術公司,開發口服小分子治療劑,用於慢性炎症和自身免疫性疾病的臨床流水線。該公司的主要開發計劃vidofludimus calcium (IMU-838) 目前處於3期和2期臨床試驗中,用於治療複發性和進展性多發性硬化症,並在復發緩解性多發性硬化症、進展性多發性硬化症和中至重度潰瘍性結腸炎患者中的2期臨床試驗中表現出治療活性。 Vidofludimus calcium通過其作爲一種核受體相關1(Nurr1)激活劑的機制,結合了神經保護作用,並通過選擇性抑制酶二氫硝酸還原酶(DHODH)而具有額外的抗炎症和抗病毒作用。 目標蛋白質Sirtuin 6 (SIRT6) 的IMU-856,旨在恢復腸道屏障功能和再生腸上皮,可能適用於多種胃腸疾病,如乳糜瀉,目前正在準備進行2期臨床試驗。當前正在進行預臨床測試的IMU-381是一種下一代分子,專門針對胃腸道疾病的需求。如需更多信息,請訪問: .
Cautionary Statement Regarding Forward-Looking Statements
This press release contains "forward-looking statements" that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical facts, included in this press release regarding strategy, future operations, future financial position, future revenue, projected expenses, sufficiency of cash and cash runway, expected timing, development and results of clinical trials, prospects, plans and objectives of management are forward-looking statements. Examples of such statements include, but are not limited to, statements relating to management's and employee's participation in investor conferences. Immunic may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in the forward-looking statements and you should not place undue reliance on these forward-looking statements. Such statements are based on management's current expectations and involve substantial risks and uncertainties. Actual results and performance could differ materially from those projected in the forward-looking statements as a result of many factors, including, without limitation, the COVID-19 pandemic, increasing inflation, impacts of the Ukraine – Russia conflict and the conflict in the Middle East on planned and ongoing clinical trials, risks and uncertainties associated with the ability to project future cash utilization and reserves needed for contingent future liabilities and business operations, the availability of sufficient financial and other resources to meet business objectives and operational requirements, including the ability to satisfy the minimum average price and trading volume conditions required to receive funding in tranche 2 and 3 of the January 2024 private placement, the fact that the results of earlier preclinical studies and clinical trials may not be predictive of future clinical trial results, the protection and market exclusivity provided by Immunic's intellectual property, risks related to the drug development and the regulatory approval process and the impact of competitive products and technological changes. A further list and descriptions of these risks, uncertainties and other factors can be found in the section captioned "Risk Factors," in the company's Annual Report on Form 10-K for the fiscal year ended December 31, 2023, filed with the SEC on February 22, 2024, and in the company's subsequent filings with the Securities and Exchange Commission. Copies of these filings are available online at www.sec.gov or ir.imux.com/sec-filings. Any forward-looking statement made in this release speaks only as of the date of this release. Immunic disclaims any intent or obligation to update these forward-looking statements to reflect events or circumstances that exist after the date on which they were made. Immunic expressly disclaims all liability in respect to actions taken or not taken based on any or all the contents of this press release.
關於前瞻性聲明的警示聲明
本新聞稿包含涉及重大風險和不確定性的「前瞻性陳述」,以符合1995年《私人證券訴訟改革法案》所提供的安全港的目的。除歷史事實陳述外,本新聞稿中包含的所有與策略、未來運營、未來財務狀況、未來營業收入、預計開支、現金及現金持續能力的充足性、預期時間、臨床試驗的發展和結果、管理層的前景、計劃和目標有關的陳述均爲前瞻性陳述。這類陳述的示例包括,但不限於,涉及管理層和員工參與投資者會議的陳述。Immunic可能實際上無法實現計劃、實施意圖或滿足前瞻性陳述中披露的期望或預測,且您不應對這些前瞻性陳述過度依賴。這些陳述基於管理層當前的期望,並涉及重大風險和不確定性。實際結果和表現可能因多種因素而與前瞻性陳述中預測的結果有重大差異,包括但不限於,COVID-19大流行、通貨膨脹上升、烏克蘭-俄羅斯衝突及中東衝突對計劃和正在進行的臨床試驗的影響,與預測未來現金利用和應對未來潛在負債和業務運營需要的儲備的能力相關的風險和不確定性,滿足業務目標和運營要求所需的足夠財務和其他資源的可用性,包括滿足2024年1月定向增發第二和第三輪融資所需的最低平均價格和成交量條件的能力,早期臨床前研究和臨床試驗結果可能無法預測未來臨床試驗結果的事實,Immunic的知識產權所提供的保護和市場獨佔性,藥物開發及監管批准過程相關的風險,以及競爭產品和技術變革的影響。這些風險、不確定性和其他因素的進一步列表和描述可以在公司於2024年2月22日提交給美國證券交易委員會的2023財年10-k表格的「風險因素」一節中找到,以及公司隨後向證券交易委員會提交的文件。這些文件的副本可以在www.sec.gov或ir.imux.com/sec-filings上在線獲得。本發佈中所作的任何前瞻性陳述僅代表發佈之日的觀點。Immunic不承諾或有義務更新這些前瞻性陳述,以反映在作出之日之後存在的事件或情況。Immunic明確否認對於基於本新聞稿的任何或所有內容採取或不採取行動的責任。
Contact Information
聯繫信息
Immunic, Inc.
Jessica Breu
Vice President Investor Relations and Communications
+49 89 2080 477 09
[email protected]
Immunic, Inc.
傑西卡·布魯(Jessica Breu)
投資者關係和溝通副總裁
+49 89 2080 477 09
[email protected]
US IR Contact
Rx Communications Group
Paula Schwartz
+1 917 633 7790
[email protected]
美國IR聯繫人
Rx Communications Group
Paula Schwartz
+1 917 633 7790
[email protected]
US Media Contact
KCSA Strategic Communications
Caitlin Kasunich
+1 212 896 1241
[email protected]
美國媒體聯繫人
KCSA戰略傳播
Caitlin Kasunich
+1 212 896 1241
[email protected]
SOURCE Immunic, Inc.
數據來源:Immunic,Inc。
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