Join Enlivex Therapeutics' Exclusive Live Investor Webinar and Q&A Session on December 3
Join Enlivex Therapeutics' Exclusive Live Investor Webinar and Q&A Session on December 3
NESS ZIONA, ISRAEL / ACCESSWIRE / November 26, 2024 / Enlivex Therapeutics Ltd. (Nasdaq:ENLV)(the "Company"), a clinical-stage macrophage reprogramming immunotherapy company, is pleased to invite investors to a webinar on December 3, 2024, at 11:00 a.m. ET.
NESS ZIONA,以色列/ ACCESSWIRE/2024年11月26日/ enlivex therapeutics有限公司(納斯達克:ENLV)("公司"),一家處於臨床階段的巨噬細胞重編程免疫療法公司,很高興邀請投資者參加2024年12月3日上午11:00看到的網絡研討會。
The exclusive event, hosted by RedChip Companies, will feature Enlivex Therapeutics Chief Executive Officer Oren Hershkovitz who will share insight into the Company's lead product, Allocetra, insight into the clinical status, and 2025 planned catalysts.
這個獨家活動由RedChip Companies主辦,將邀請 enlivex therapeutics 首席執行官 Oren Hershkovitz 分享公司的主打產品Allocetra、臨床狀態和2025年計劃的催化劑。
Allocetra is an off-the-shelf, cell therapy technology that reprograms non-homeostatic macrophages to their optimal functioning state, addressing critical unmet needs in conditions like osteoarthritis, sepsis, and psoriatic arthritis. With Phase I/II clinical trials showing promising results and targeting multi-billion-dollar markets, Allocetra has the potential to redefine treatment paradigms for inflammatory and autoimmune diseases.
Allocetra是一種現成、細胞療法技術,將非體內穩態巨噬細胞重編程爲最佳功能狀態,解決類似骨關節炎、敗血症和銀屑病等疾病的關鍵未滿足需求。通過I/II期臨床試驗顯示出有希望的結果,目標是現有的價值數十億美元市場,Allocetra有潛力重新定義炎症和自身免疫疾病的治療範式。
To register for the free webinar, please visit:
要註冊免費網絡研討會,請訪問:
A live Q&A session will follow the presentation. Questions can be pre-submitted to ENLV@redchip.com or online during the live event.
演示結束後將進行現場問答環節。問題可事先發送至ENLV@redchip.com或在線提交。
ABOUT ENLIVEX
關於Enlivex
Enlivex is a clinical stage macrophage reprogramming immunotherapy company developing Allocetra, a universal, off-the-shelf cell therapy designed to reprogram macrophages into their homeostatic state. Resetting non-homeostatic macrophages into their homeostatic state is critical for immune system rebalancing and resolution of life-threatening and life debilitating conditions. For more information, visit .
Enlivex是一家臨床階段的巨噬細胞重編程免疫療法公司,開發了Allocetra,一種旨在將巨噬細胞重編程爲其穩態狀態的通用、現貨細胞療法。將非穩態狀態的巨噬細胞重置爲其穩態狀態對於免疫系統的重新平衡和解決危及生命和導致生活無法自理的疾病至關重要。有關更多信息,請訪問。
Safe Harbor Statement: This press release contains forward-looking statements, which may be identified by words such as "expects," "plans," "projects," "will," "may," "anticipates," "believes," "should," "would", "could," "intends," "estimates," "suggests," "has the potential to" and other words of similar meaning, including statements regarding expected cash balances, market opportunities for the results of current clinical studies and preclinical experiments, the effectiveness of, and market opportunities for, ALLOCETRA TM programs. All such forward-looking statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Investors are cautioned that forward-looking statements involve risks and uncertainties that may affect Enlivex's business and prospects, including the risks that Enlivex may not succeed in generating any revenues or developing any commercial products; that the products in development may fail, may not achieve the expected results or effectiveness and/or may not generate data that would support the approval or marketing of these products for the indications being studied or for other indications; that ongoing studies may not continue to show substantial or any activity; and other risks and uncertainties that may cause results to differ materially from those set forth in the forward-looking statements. The results of clinical trials in humans may produce results that differ significantly from the results of clinical and other trials in animals. The results of early-stage trials may differ significantly from the results of more developed, later-stage trials. The development of any products using the ALLOCETRA TM product line could also be affected by a number of other factors, including unexpected safety, efficacy or manufacturing issues, additional time requirements for data analyses and decision making, the impact of pharmaceutical industry regulation, the impact of competitive products and pricing and the impact of patents and other proprietary rights held by competitors and other third parties. In addition to the risk factors described above, investors should consider the economic, competitive, governmental, technological and other factors discussed in Enlivex's filings with the Securities and Exchange Commission, including in the Company's most recent Annual Report on Form 20-F filed with the Securities and Exchange Commission. The forward-looking statements contained in this press release speak only as of the date the statements were made, and we do not undertake any obligation to update forward-looking statements, except as required under applicable law.
免責聲明:本新聞稿包含前瞻性聲明,可能被識別爲"期望"、"計劃"、"項目"、"將"、"可能"、"預期"、"相信"、"應該"、"將會"、"能夠"、"打算"、"估計"、"建議"、"具有潛力"等表達意思相近的詞語,包括關於預期現金餘額、當前臨床研究和臨床試驗結果的市場機會、ALLOECTRA Tm項目的有效性和市場機會的陳述。所有此類前瞻性聲明均根據1995年《私募證券訴訟改革法》的安全港規定發表。投資者應注意,前瞻性聲明涉及可能影響enlivex的業務和前景的風險和不確定性,包括enlivex可能無法實現任何收入或開發任何商業產品;開發中的產品可能失敗,可能不達到預期的結果或有效性,可能不產生支持這些產品獲得研究中或其他適應症批准或上市的數據;正在進行的研究可能不會繼續顯示出重大或任何活性;以及其他可能導致結果與前瞻性聲明中所述結果有實質差異的風險和不確定性。人類臨床試驗的結果可能導致與動物臨床和其他試驗結果顯著不同的結果。早期階段試驗的結果可能與更爲發展成熟的後期試驗的結果顯著不同。利用ALLOECTRA Tm產品系列開發任何產品還可能受到其他許多因素影響,包括意外的安全性、有效性或製造問題,數據分析和決策制定的額外時間需求,製藥行業規定的影響,競爭產品和定價的影響,以及由競爭對手和第三方持有的專利等專有權利的影響。除上述風險因素外,投資者還應考慮經濟、競爭、政府、技術和其他因素,這些因素已在enlivex向證券交易委員會提交的文件中進行了討論,包括公司最近一份提交的《20-F表》。本新聞稿中包含的前瞻性聲明僅針對發表聲明的日期,我們不承擔更新前瞻性聲明的任何義務,除非依法需要。
Contact:
Dave Gentry, CEO
RedChip Companies, Inc.
1-407-644-4256
ENLV@redchip.com
聯繫方式:
首席執行官Dave Gentry
RedChip Companies, Inc.
1-407-644-4256
ENLV@redchip.com
SOURCE: Enlivex Therapeutics Ltd.
來源: enlivex therapeutics有限公司。
譯文內容由第三人軟體翻譯。