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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独家直播投资者网络研讨会和2024年11月7日问答环节
GlobeNewswire ·  2024/10/23 05:00

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.

内华达州卡森城,2024年10月23日(GLOBE NEWSWIRE) —biovie(纳斯达克:BIVI)公司,(“BioVie”或“公司”),一家正在开发创新药物治疗神经和神经退行性疾病以及先进肝病的临床阶段公司,诚邀投资者参加2024年11月7日晚上4:15,Et举办的网络研讨会。

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.

独家活动由RedChip公司主办,将由biovie的总裁兼首席执行官Cuong Do主持,他将分享有关该公司在帕金森病(PD)、长期新冠病毒病(LC)、阿尔茨海默病(AD)和先进肝病相关腹水中中晚期临床项目的见解和进展。

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的主要资产,贝齐替林(NE3107),已证明能够调节TNFα的产生,导致显著的临床改善。在临床研究中,接受贝齐替林治疗的患者经历了炎症和胰岛素抵抗力的减少,PD中的改善运动控制和“清晨运动”症状,以及AD中认知衰退的减缓和更好的脑部成像扫描,同时减少了DNA甲基化水平。公司的战略重点包括在2024年底或2025年初启动PD的第20亿阶段试验,在2025年初启动由美国国防部(DOD)的资助启动的LC的探索性第2期试验,以及在2025年底使用贝齐替林新的每日一次配方启动AD的第3期试验。公司还在继续就贝齐替林的地理权利进行合作伙伴讨论,并计划在确定合适合作伙伴后开始BIV201(持续输注替利普脑)治疗腹水的第三期试验。

To register for the free webinar, please visit:

要注册免费的网络研讨会,请访问:

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

问题可以在直播活动期间通过BIVI@redchip.com或在线预先提交。

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

关于BioVie Inc.
biovie公司(纳斯达克股票代码:BIVI)是一家临床阶段公司,致力于开发创新的药物疗法,用于治疗神经系统和神经退行性疾病(长期COVID、阿尔茨海默病和帕金森病)以及先进肝脏疾病。在神经退行性疾病中,公司的药物候选化合物bezisterim抑制了细胞外信号调节激酶和转录因子核因子- kb的炎症激活,以及相关的神经炎症和胰岛素抵抗,但不影响ERk和NFkb的稳态功能(例如胰岛素信号传导和神经元生长与存活)。神经炎症和胰岛素抵抗都是阿尔茨海默病和帕金森病的发动机。持续系统性炎症和神经炎症是长期COVID患者神经症状的关键特征。在肝脏疾病中,公司的孤儿药物候选化合物BIV201(连续静脉注射替利普普胺),拥有FDA快速通道地位,正在根据FDA的指导评估和讨论设计BIV201用于减少参与者肝硬化和腹水进一步恶化的3期临床试验的。这种活性药物在美国和大约40个国家已经获得批准,用于治疗先进肝硬化的相关并发症。更多信息,请访问

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.

前瞻性声明
本新闻稿包含前瞻性声明,可能会被诸如“预计”,“期待”,“预测”,“打算”,“计划”,“相信”,“谋求”,“估计”,“将”,“项目”或类似含义的词所确定。虽然BioVie Inc.认为这些前瞻性声明基于合理的假设,但不能保证其预期将实现。由于公司成功以合理条件或根本无法成功筹集足够资本,手头现金毫无保留地并合同和法定限制可能会损害我们支付未来股息的能力,能否完成我们的临床前或临床研究以及获得我们的产品候选人的批准,我们能否成功辩护未来潜在诉讼,以及本地或全国经济情况的变化以及各种其他风险,其中许多现在尚不知晓且通常不受公司所控制,并且通常会在时间内报告由公司向SEC提交的报告中定期披露,包括Form 10-Q季度报告,Form 8-K报告和Form 10-K年度报告。BioVie Inc.不承担任何更新此处所包含的任何声明(包括任何前瞻性声明)的责任,除非法律另有规定。

Contact:

联系方式:

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

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

For Investor Relations Inquiries:

投资者关系查询:

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

Brian Siegel,IRC,MBA-高级管理董事,Hayden IR,电话:(346)396-8696,ir@zedge.net
布鲁斯·马克尔。
董事总经理
LifeSci Advisors, LLC
bmackle@lifesciadvisors.com

For Media Inquiries:

媒体查询:

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

联系方式:
电话:+1 201-723-5705
管理合伙人
Elixir Health Public Relations
电话:+1 201-723-5705
mweible@elixirhealthpr.com


声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
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