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Join BioVie's Exclusive Live Investor Webinar and Q&A Session on November 7th, 2024

Join BioVie's Exclusive Live Investor Webinar and Q&A Session on November 7th, 2024

加入biovie獨家線上投資者研討會,並參加2024年11月7日的問答環節
GlobeNewswire ·  10/23 20:00

CARSON CITY, Nev., Oct. 23, 2024 (GLOBE NEWSWIRE) -- BioVie Inc. (NASDAQ: BIVI), ("BioVie" or the "Company"), a clinical-stage company developing innovative drug therapies for the treatment of neurological and neurodegenerative disorders and advanced liver disease, is pleased to invite investors to a webinar on November 7, 2024, at 4:15 p.m. ET.

內華達州卡森城,2024年10月23日(GLOBE NEWSWIRE) —biovie(納斯達克:BIVI)公司,(「BioVie」或「公司」),一家正在開發創新藥物治療神經和神經退行性疾病以及先進肝病的臨床階段公司,誠邀投資者參加2024年11月7日晚上4:15,Et舉辦的網絡研討會。

The exclusive event, hosted by RedChip Companies, will feature Cuong Do, President and CEO of BioVie, who will share insights and developments on the Company's pipeline mid-to-late-stage clinical programs in Parkinson's disease (PD), long COVID (LC), Alzheimer's disease (AD), and ascites associated with advanced liver disease.

獨家活動由RedChip公司主辦,將由biovie的總裁兼首席執行官Cuong Do主持,他將分享有關該公司在帕金森病(PD)、長期新冠病毒病(LC)、阿爾茨海默病(AD)和先進肝病相關腹水中中晚期臨床項目的見解和進展。

BioVie's lead asset, bezisterim (formerly NE3107), has demonstrated the ability to modulate TNFα production, leading to significant clinical improvements. In clinical studies, patients treated with bezisterim experienced reduced inflammation and insulin resistance, improved motor control and "morning on" symptoms in =PD, and slowing of cognitive decline and better brain imaging scans in AD as well as reduced DNA methylation levels. The Company's strategic priorities include launching a Phase 2b trial for PD in late 2024 or early 2025, launching an exploratory Phase 2 trial that has been fully funded by a grant from the U.S. Department of Defense (DOD) in LC in early 2025 and initiating a Phase 3 trial for AD in late 2025 with a new once-daily formulation of bezisterim. The Company is also continuing partnering discussions for bezisterim's geographic rights, and plans to commence an ascites Phase 3 trial for BIV201 (continuous infusion terlipressin) upon identifying a suitable partner.

biovie的主要資產,貝齊替林(NE3107),已證明能夠調節TNFα的產生,導致顯著的臨床改善。在臨床研究中,接受貝齊替林治療的患者經歷了炎症和胰島素抵抗力的減少,PD中的改善運動控制和「清晨運動」症狀,以及AD中認知衰退的減緩和更好的腦部成像掃描,同時減少了DNA甲基化水平。公司的戰略重點包括在2024年底或2025年初啓動PD的第20億階段試驗,在2025年初啓動由美國國防部(DOD)的資助啓動的LC的探索性第2期試驗,以及在2025年底使用貝齊替林新的每日一次配方啓動AD的第3期試驗。公司還在繼續就貝齊替林的地理權利進行合作伙伴討論,並計劃在確定合適合作伙伴後開始BIV201(持續輸注替利普腦)治療腹水的第三期試驗。

To register for the free webinar, please visit:

要註冊免費的網絡研討會,請訪問:

Questions can be pre-submitted to BIVI@redchip.com or online during the live event.

問題可以在直播活動期間通過BIVI@redchip.com或在線預先提交。

About BioVie Inc.
BioVie Inc. (NASDAQ: BIVI) is a clinical-stage company developing innovative drug therapies for the treatment of neurological and neurodegenerative disorders (Long COVID, Alzheimer's disease and Parkinson's disease) and advanced liver disease. In neurodegenerative disease, the Company's drug candidate bezisterim inhibits inflammatory activation of extracellular signal-regulated kinase and the transcription factor, Nuclear factor- kB, and the associated neuroinflammation and insulin resistance but not ERK and NFkB homeostatic functions (e.g., insulin signaling and neuron growth and survival). Both neuroinflammation and insulin resistance are drivers of AD and PD. Persistent systematic inflammation and neuroinflammation are key features in patients with neurological symptoms of Long COVID. In liver disease, the Company's Orphan drug candidate BIV201 (continuous infusion terlipressin), with FDA Fast Track status, is being evaluated and discussed with guidance received from the FDA regarding the design of Phase 3 clinical testing of BIV201 for the reduction of further decompensation in participants with liver cirrhosis and ascites. The active agent is approved in the U.S. and in about 40 countries for related complications of advanced liver cirrhosis. For more information, visit

關於BioVie Inc.
biovie公司(納斯達克股票代碼:BIVI)是一家臨床階段公司,致力於開發創新的藥物療法,用於治療神經系統和神經退行性疾病(長期COVID、阿爾茨海默病和帕金森病)以及先進肝臟疾病。在神經退行性疾病中,公司的藥物候選化合物bezisterim抑制了細胞外信號調節激酶和轉錄因子核因子- kb的炎症激活,以及相關的神經炎症和胰島素抵抗,但不影響ERk和NFkb的穩態功能(例如胰島素信號傳導和神經元生長與存活)。神經炎症和胰島素抵抗都是阿爾茨海默病和帕金森病的發動機。持續系統性炎症和神經炎症是長期COVID患者神經症狀的關鍵特徵。在肝臟疾病中,公司的孤兒藥物候選化合物BIV201(連續靜脈注射替利普普胺),擁有FDA快速通道地位,正在根據FDA的指導評估和討論設計BIV201用於減少參與者肝硬化和腹水進一步惡化的3期臨床試驗的。這種活性藥物在美國和大約40個國家已經獲得批准,用於治療先進肝硬化的相關併發症。更多信息,請訪問

Forward-Looking Statements
This press release contains forward-looking statements, which may be identified by words such as "expect," "look forward to," "anticipate" "intend," "plan," "believe," "seek," "estimate," "will," "project" or words of similar meaning. Although BioVie Inc. believes such forward-looking statements are based on reasonable assumptions, it can give no assurance that its expectations will be attained. Actual results may vary materially from those expressed or implied by the statements herein due to the Company's ability to successfully raise sufficient capital on reasonable terms or at all, available cash on hand and contractual and statutory limitations that could impair our ability to pay future dividends, our ability to complete our pre-clinical or clinical studies and to obtain approval for our product candidates, our ability to successfully defend potential future litigation, changes in local or national economic conditions as well as various additional risks, many of which are now unknown and generally out of the Company's control, and which are detailed from time to time in reports filed by the Company with the SEC, including quarterly reports on Form 10-Q, reports on Form 8-K and annual reports on Form 10-K. BioVie Inc. does not undertake any duty to update any statements contained herein (including any forward-looking statements), except as required by law.

前瞻性聲明
本新聞稿包含前瞻性聲明,可能會被諸如「預計」,「期待」,「預測」,「打算」,「計劃」,「相信」,「謀求」,「估計」,「將」,「項目」或類似含義的詞所確定。雖然BioVie Inc.認爲這些前瞻性聲明基於合理的假設,但不能保證其預期將實現。由於公司成功以合理條件或根本無法成功籌集足夠資本,手頭現金毫無保留地併合同和法定限制可能會損害我們支付未來股息的能力,能否完成我們的臨床前或臨床研究以及獲得我們的產品候選人的批准,我們能否成功辯護未來潛在訴訟,以及本地或全國經濟情況的變化以及各種其他風險,其中許多現在尚不知曉且通常不受公司所控制,並且通常會在時間內報告由公司向SEC提交的報告中定期披露,包括Form 10-Q季度報告,Form 8-K報告和Form 10-K年度報告。BioVie Inc.不承擔任何更新此處所包含的任何聲明(包括任何前瞻性聲明)的責任,除非法律另有規定。

Contact:

聯繫方式:

Dave Gentry, CEO
RedChip Companies, Inc.
1-407-644-4256
BIVI@redchip.com

首席執行官Dave Gentry
RedChip Companies, Inc.
1-407-644-4256
BIVI@redchip.com

For Investor Relations Inquiries:

投資者關係查詢:

Contact:
Bruce Mackle
Managing Director
LifeSci Advisors, LLC
bmackle@lifesciadvisors.com

Brian Siegel,IRC,MBA-高級管理董事,Hayden IR,電話:(346)396-8696,ir@zedge.net
布魯斯·馬克爾。
董事總經理
LifeSci Advisors, LLC
bmackle@lifesciadvisors.com

For Media Inquiries:

媒體查詢:

Contact:
Melyssa Weible
Managing Partner
Elixir Health Public Relations
Ph: +1 201-723-5705
mweible@elixirhealthpr.com

聯繫方式:
電話:+1 201-723-5705
管理合夥人
Elixir Health Public Relations
電話:+1 201-723-5705
mweible@elixirhealthpr.com


譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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