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OmniScience Inc. and INmune Bio Inc. Partner to Accelerate a Phase 2 Alzheimer's Trial With Vivo, a Novel GenAI Clinical Trial Control Tower

OmniScience Inc. and INmune Bio Inc. Partner to Accelerate a Phase 2 Alzheimer's Trial With Vivo, a Novel GenAI Clinical Trial Control Tower

OmniScience公司和INmune Bio公司合作,加速一项第二阶段阿尔茨海默病临床试验,采用Vivo,一种新型GenAI临床试验控制塔架
GlobeNewswire ·  12/04 06:00

Vivo Empowers Clinical Development Teams to Accelerate Decision-making and Analyses in Clinical Trials for Improved Outcomes

Vivo赋予临床开发团队加速决策和分析的能力,在临床试验中取得改善的结果

HOUSTON and BOCA RATON, Fla., Dec. 04, 2024 (GLOBE NEWSWIRE) -- OmniScience and INmune Bio (NASDAQ: INMB) today announced a pioneering partnership to revolutionize operations for INmune Bio's global Phase 2 Alzheimer's disease (AD) clinical trial (the "AD02 trial") using OmniScience's flagship product, Vivo, an industry-first, genAI-powered control tower designed specifically for centralizing and analyzing vast clinical data in real time. This solution represents a innovative approach to clinical research, delivering immediate insights that enhance decision-making and transform traditional, time-consuming trial management.

休斯顿和佛罗里达州博卡拉顿,2024年12月04日(环球新闻通讯社)-- OmniScience和inmune bio(纳斯达克:INMB)今天宣布了一项开创性的合作伙伴关系,以革命性地改进inmune bio全球第二期阿尔茨海默病(AD)临床试验(“AD02试验”)的运营,利用OmniScience的旗舰产品Vivo,这是第一个专为实时集中和分析庞大的临床数据而设计的人工智能驱动控件。这项解决方案代表了一种创新的临床研究方法,提供及时的洞察,增强决策能力,转变传统的耗时试验管理。

Vivo securely unifies data across sources including electronic data capture (EDC), clinical trial management systems (CTMS), patient-reported outcomes (PROs)/clinical outcome assessments (COAs), labs, sensors/wearables, safety databases, and more. With fully integrated data, Vivo goes beyond dashboard visualizations to enable clinical trial teams to improve their decision-making, accelerate timelines, enhance patient safety, and ultimately improve health outcomes. Designed with explainability and interpretability at its core, Vivo ensures that every generated insight is supported by clear, traceable rationale grounded in data and clinical context. Its advanced cognitive architecture combines ontological knowledge of trial protocols with domain-specific clinical expertise, enabling qualitative and quantitative reasoning at scale.

Vivo 安全地统一了来自各个来源的数据,包括电子数据捕捉(EDC)、临床试验管理系统(CTMS)、患者报告结果(PROs)/临床结果评估(COAs)、实验室、传感器/可穿戴设备、安全数据库等。通过完全集成的数据,Vivo 不仅仅限于仪表盘可视化,还可让临床试验团队改善他们的决策能力,加快时间表,增强患者安全性,并最终改善健康结果。Vivo 的先进认知架构将试验方案的本体知识与领域特定的临床专业知识相结合,实现了定性和定量推理的规模化。

INmune Bio recently announced it completed randomization of patients for its blinded AD02 trial for patients with early AD and biomarkers of elevated neuroinflammation. The trial overenrolled with a total of 208 patients, 56% of whom were categorized as mild AD and 44% as mild cognitive impairment. INmune Bio plans to release top-line cognitive results in the second quarter of 2025.

inmune bio最近宣布已完成早期AD和升高神经炎症生物标志物患者的盲法AD02试验的患者随机分组。试验超额招生,共有208名患者,其中56%被归类为轻度AD,44%被归类为轻度认知障碍。inmune bio计划在2025年第二季度发布顶线认知结果。

"A global trial of this size is vast, and Vivo will be critical in our ability to analyze cognitive results," stated Tara Lehner, INmune Bio's VP of Clinical Operations. "With genAI provided by Vivo, we can amplify our clinical teams' capabilities, turning complex data into actionable insights at unprecedented speed, which means we can get answers—and treatments—to patients faster."

"这样规模的全球试验是庞大的,Vivo 将对我们分析认知结果的能力至关重要," inmune bio 的临床运营副总裁 Tara Lehner 表示。"借助 Vivo 提供的 genAI,我们可以增强临床团队的能力,将复杂数据转化为具有前所未有速度的可操作洞察力,这意味着我们可以更快地给患者提供答案和治疗。"

INmune and OmniScience partnered throughout Vivo's product development and have completed the first phase of Vivo's roll-out to INmune's clinical development team. Throughout the initial rollout, significant beneficial findings include:

INmune和OmniScience在Vivo产品开发中建立了合作伙伴关系,并已完成Vivo面向INmune临床开发团队的第一阶段推出。在初始推出期间,显著有益的发现包括:

  • Improved data quality through Vivo's automatic identification of data discrepancies
  • Enhanced visualization of COAs, supporting identification of outliers and better understanding of population distributions
  • Real-time answers, supporting decisions on patient enrollment criteria, even while the patient is in the clinic
  • Reduced reliance on time-consuming spreadsheet-based data analysis, improving collaboration between clinical and executive teams
  • 通过Vivo自动识别数据差异来改善数据质量
  • 增强COAs的可视化,支持异常值识别和更好的理解人口分布
  • 实时回答,支持对患者入组标准的决策,即使患者仍在诊所
  • 减少对耗时的基于电子表格的数据分析的依赖,改善临床和高层团队之间的协作

"OmniScience and INmune Bio share a vision to transform how clinical trial teams engage with data – transforming data into knowledge in real time and informing decisions that increase the probability of success," shared Angela Holmes, CEO of OmniScience. "As our partnership moves forward, we're gaining further insights from the INmune team that we can integrate into Vivo's roadmap. We look forward to our continued mutual success."

"OmniScience和INmune Bio一起分享将如何改变临床试验团队与数据互动的愿景 - 实时将数据转化为知识,并为提高成功概率的决策提供信息," OmniScience首席执行官安吉拉·霍尔姆斯分享道。"随着我们合作的深入,我们正在从INmune团队中获得进一步的见解,我们可以整合到Vivo的路线图中。我们期待我们持续的共同成功。"

"The future of clinical trials demands smarter solutions, and Vivo embodies this shift," explained Michael Bell, VP of Product, OmniScience. "Through this collaboration, INmune Bio provides continuous feedback that enables OmniScience's development team to evolve Vivo. This hands-on approach builds confidence among users, who see firsthand how genAI can rapidly turn data into answers and transform their day-to-day workflows."

"临床试验的未来需要更智能的解决方案,而Vivo体现了这种转变," OmniScience产品副总裁迈克尔·贝尔解释道。"通过这种合作,INmune Bio提供持续的反馈,使OmniScience的开发团队能够发展Vivo。这种亲身参与的方法在用户之间建立了信心,他们亲眼看到genAI如何快速将数据转化为答案,并转变他们的日常工作流程。"

About OmniScience Inc.

关于OmniScience Inc。

OmniScience is a trusted partner to leading life science organizations, advancing clinical R&D missions through unparalleled expertise in clinical data science. We believe in a future where all clinical trial data can be unified and translated into knowledge in real time.

OmniScience 是领先生命科学组织信赖的合作伙伴,通过卓越的临床数据科学推动临床研发任务。我们相信,未来所有的临床试验数据都可以统一并实时转化为知识。

Our expert team has created Vivo, the first and only company in the world to enable GenAI as a control tower, offering on demand insights into live unified clinical trial data. No spreadsheets, no SQL queries, no emails. Vivo revolutionizes the way pharma manages clinical trials and employs generative AI, with the industry's first gen AI assistant for clinical trial operations. Vivo is more than just a platform – it's your new favorite clinical development colleague, poised to transform clinical trial operation teams' day-to-day workflow and ability to optimize trial insights with generative AI. Vivo was recently awarded top honors at the Innovation Showcase at the November 2024 CNS Summit as well as the 2024 Innovation Network Gathering Whale Tank competition.

我们的专家团队创造了Vivo,这是全球首家公司能够将人工智能作为控件,提供实时统一临床试验数据的按需洞察。没有电子表格,没有SQL查询,没有电子邮件。Vivo彻底改变了制药行业管理临床试验的方式,并采用了针对临床试验操作的行业首个人工智能助手。Vivo不仅仅是一个平台-它是您新的最爱临床开发同事,准备转变临床试验操作团队的日常工作流程,并利用人工智能优化试验洞察。Vivo最近在 awarded top honors 2024年11月CNS峰会的创新展示和2024年创新网络Gathering Whale Tank竞赛中。

To discuss how OmniScience can support your clinical trials, please visit or reach us at hello@omniscience.bio or on LinkedIn.

要讨论OmniScience如何支持您的临床试验,请访问或通过hello@omniscience.bio或在LinkedIn上与我们联系。

About INmune Bio Inc.

关于INmune Bio公司

INmune Bio Inc. is a publicly traded (NASDAQ: INMB), clinical-stage biotechnology company focused on developing treatments that target the innate immune system to fight disease. INmune Bio has two product platforms that are both in clinical trials: The Dominant-Negative Tumor Necrosis Factor (DN-TNF) product platform utilizes dominant-negative technology to selectively neutralize soluble TNF, a key driver of innate immune dysfunction and a mechanistic driver of many diseases. DN-TNF product candidates are in clinical trials to determine if they can treat cancer (INB03), Mild Alzheimer's disease, Mild Cognitive Impairment and treatment-resistant depression (XPro). The Natural Killer Cell Priming Platform includes INKmune developed to prime a patient's NK cells to eliminate minimal residual disease in patients with cancer. INmune Bio's product platforms utilize a precision medicine approach for the treatment of a wide variety of hematologic and solid tumor malignancies, and chronic inflammation. To learn more, please visit .

inmune bio公司是一家在纳斯达克上市(纳斯达克:INMB),专注于开发针对先天免疫系统的治疗方法的临床阶段生物技术公司。inmune bio拥有两个处于临床试验中的产品平台:主导阴性肿瘤坏死因子(DN-TNF)产品平台利用主导阴性技术选择性中和可溶性TNF,TNF是先天免疫功能障碍的关键驱动因素,也是许多疾病的机械驱动因素。 DN-TNF产品候选药正在临床试验中,以确定它们是否可以治疗癌症(INB03)、轻度阿尔茨海默病、轻度认知障碍和治疗耐药抑郁(XPro)。自然杀伤细胞激活平台包括开发的INKmune,用于激活患者的Nk细胞,以消除患有癌症的患者中的微小残留疾病。inmune bio的产品平台采用精准医学方法治疗各种血液学和实体瘤恶性肿瘤以及慢性炎症。要了解更多信息,请访问。

Forward Looking Statements

前瞻性声明

Clinical trials are in early stages and there is no assurance that any specific outcome will be achieved. Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any forward-looking statements contained herein are based on current expectations but are subject to a number of risks and uncertainties. Actual results and the timing of certain events and circumstances may differ materially from those described by the forward-looking statements as a result of these risks and uncertainties. INB03, XPro1595 (XPro), and INKmune are still in clinical trials or preparing to start clinical trials and have not been approved by the US Food and Drug Administration (FDA) or any regulatory body and there cannot be any assurance that they will be approved by the FDA or any regulatory body or that any specific results will be achieved. The factors that could cause actual future results to differ materially from current expectations include, but are not limited to, risks and uncertainties relating to the Company's ability to produce more drug for clinical trials; the availability of substantial additional funding for the Company to continue its operations and to conduct research and development, clinical studies and future product commercialization; and, the Company's business, research, product development, regulatory approval, marketing and distribution plans and strategies. These and other factors are identified and described in more detail in the Company's filings with the Securities and Exchange Commission, including the Company's Annual Report on Form 10-K, the Company's Quarterly Reports on Form 10-Q and the Company's Current Reports on Form 8-K. The Company assumes no obligation to update any forward-looking statements in order to reflect any event or circumstance that may arise after the date of this release.

临床试验处于早期阶段,不能保证实现任何具体的结果。本新闻稿中包含的任何不描述历史事实的声明可能构成前瞻性声明,如1995年《私人证券诉讼改革法》中所定义。本新闻稿中包含的任何不描述历史事实的声明可能构成前瞻性声明,如1995年《私人证券诉讼改革法》中所定义。任何此类前瞻性声明均基于目前的期望,但由于这些风险和不确定性的存在,实际结果和某些事件和情况的时间可能因这些风险和不确定性而有所不同。 INB03、XPro1595(XPro)和INKmune仍处于临床试验阶段或正在准备开始临床试验,尚未获得美国食品和药物管理局(FDA)或任何监管机构的批准,不能确保将获得FDA或任何监管机构的批准或实现任何具体的结果。可能导致实际未来结果有所不同的因素有很多,但不限于,与公司为临床试验生产更多药物的能力有关的风险和不确定性; 为了继续其业务并进行研究和开发、临床研究和未来产品商业化活动所需的大量额外资金的可用性; 以及公司的业务、研究、产品开发、监管批准、市场营销和分销计划和策略。这些和其他因素在公司提交给证券和交易委员会的文件中有更详细的描述,包括公司的年度报告提交的10-k,公司提交的季度报告提交的10-Q以及公司提交的当前报告提交的8-k。公司假定没有任何义务更新任何前瞻性声明以反映可能在本发行日期之后出现的任何事件或情况。

For OmniScience:

对于OmniScience:

Media Contact:
Sean Leous
ICR Healthcare
Sean.leous@icrhealthcare.com
646-866-4012

媒体联系:
Sean Leous
ICR 医疗保健
Sean.leous@icrhealthcare.com
646-866-4012

For INmune Bio Inc.:

对于inmune bio公司:

David Moss
Co-founder and Chief Financial Officer
(858) 964-3720
info@inmunebio.com

Daniel Carlson
Head of Investor Relations
(415) 509-4590
dcarlson@inmunebio.com

David Moss
联合创始人和致富金融(临时代码)官员
(858)964-3720
info@inmunebio.com

丹尼尔·卡尔森
投资者关系主管
(415) 509-4590
dcarlson@inmunebio.com

Investor Contact:
Mike Moyer
Managing Director – LifeSci Advisors
mmoyer@lifesciadvisors.com

投资者联系人:
迈克·莫迪尔
董事总经理 – LifeSci Advisors
mmoyer@lifesciadvisors.com


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