share_log

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公司與INmune Bio公司合作,加速一項使用Vivo的二期阿爾茨海默症臨床試驗,這是一種新型GenAI臨床試驗塔架。
GlobeNewswire ·  2024/12/04 14:00

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

Vivo賦予臨床開發團隊權力,加快決策和分析在臨床試驗中,以提高結果

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.

休斯頓和佛羅里達博卡拉頓,2024年12月04日(全球新聞專線)- OmniScience和inmune bio(納斯達克:INMB)今天宣佈開展開創性合作伙伴關係,革新inmune bio全球阿爾茨海默病(AD)第二期臨床試驗(「AD02試驗」)的控制塔,採用了OmniScience的旗艦產品Vivo,這是業內首創的基於genAI的控制塔,專爲將大量臨床數據集中分析實時數據而設計。該解決方案代表了臨床研究的創新方法,提供即時見解,增強決策能力,並改變傳統耗時的試驗管理。

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安全地統一了來自源數據的數據,包括電子數據捕獲(EDC),臨床試驗管理系統(CTMS),患者彙報結果(PROs)/臨床結果評估(COAs),實驗室,傳感器/可穿戴設備,安全數據庫等。憑藉完全集成的數據,Vivo不僅限於儀表板可視化,還能使臨床試驗團隊改善其決策能力,加快時間表,增強患者安全性,並最終改善健康結果。Vivo設計以解釋性和可解釋性爲核心,確保每個生成的見解都有清晰,可追溯的基於數據和臨床背景的理由支持。其先進的認知架構將試驗方案的本體知識與領域特定的臨床專業知識相結合,使定性和定量推理規模化。

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最近宣佈完成了早期AD和神經炎症標誌物患者在其盲目AD02試驗中的隨機分組。該試驗超額招募了共208名患者,其中56%被歸類爲輕度AD,44%被歸類爲輕度認知障礙。inmune bio計劃於2025年第二季度發佈頂級認知結果。

"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."

「這樣規模的全球試驗是巨大的,Vivo在分析認知結果方面將起到關鍵作用,」 inmune bio的臨時代碼首席臨床操作官Tara Lehner表示。「通過Vivo提供的genAI,我們可以增強臨床團隊的能力,將複雜數據轉化爲行動洞察,以前所未有的速度做出決策,這意味着我們可以更快地回答問題併爲患者提供治療。」

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 bio和OmniScience在Vivo的產品開發過程中合作,並已完成Vivo的首階段推出,面向inmune的臨床開發團隊。在最初的推出過程中,一些重要的有益發現包括:

  • 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
  • 通過Vivo自動識別數據差異,數據質量得到提高
  • COAs的增強可視化,支持識別異常值,更好地了解人群分佈
  • 實時回答,支持在患者仍在診所時即可制定患者入組標準的決策
  • 減少對耗時的基於電子表格的數據分析的依賴,提高臨床團隊和管理團隊之間的協作

"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分享了一個願景,即改變臨床試驗團隊與數據互動的方式,將數據實時轉化爲知識,併爲增加成功概率的決策提供信息,OmniScience的首席執行官Angela Holmes分享道:「隨着合作的深入,我們從inmune團隊獲得了更多的見解,可以融入Vivo的路線圖。期待我們繼續取得共同成功。」

"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."

「臨床試驗的未來需要更智能的解決方案,而Vivo體現了這種轉變,」 OmniScience產品副總裁Michael Bell解釋道。「通過這種合作,inmune bio提供持續反饋,使OmniScience的開發團隊能夠發展Vivo。這種親身參與的方式增強了用戶信心,用戶可以親眼看到genAI如何迅速將數據轉化爲答案,並轉變他們的日常工作流程。」

About OmniScience Inc.

關於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是領先的生命科學組織值得信賴的合作伙伴,通過在臨床數據科學領域的卓越專長推動臨床研發任務。我們相信未來所有臨床試驗數據可以統一併實時轉化爲知識。

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.

我們的專家團隊創建了Vivo,這是世界上第一家也是唯一一家可以將GenAI作爲控制塔的公司,爲實時統一臨床試驗數據提供即時洞察。沒有電子表格,沒有SQL查詢,沒有電子郵件。Vivo徹底改變了製藥行業管理臨床試驗的方式,並運用生成式人工智能,擁有行業首款用於臨床試驗操作的基因AI助手。Vivo不僅僅是一個平台-它是您新的最喜愛的臨床開發同事,旨在改變臨床試驗操作團隊的日常工作流程,並通過生成式AI優化試驗洞察的能力。Vivo最近 榮獲2024年11月CNS峯會創新展示會以及2024年創新網絡聚會鯨魚池比賽的最高榮譽 。要討論OmniScience如何支持您的臨床試驗,請訪問網站或通過hello@omniscience.bio或LinkedIn聯繫我們。

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

要討論OmniScience如何支持您的臨床試驗,請訪問 或通過hello@omniscience.bio或LinkedIn聯繫我們。

About INmune Bio Inc.

關於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公司是一家在納斯達克上市(納斯達克:INMB),專注於開發針對先天免疫系統的治療方法的臨床階段生物技術公司。inmune bio擁有兩個處於臨床試驗中的產品平台:主導陰性腫瘤壞死因子(DN-TNF)產品平台利用主導陰性技術選擇性中和可溶性TNF,TNF是先天免疫功能障礙的關鍵驅動因素,也是許多疾病的機械驅動因素。 DN-TNF產品候選藥正在臨床試驗中,以確定它們是否可以治療癌症(INB03)、輕度阿爾茨海默病、輕度認知障礙和治療耐藥抑鬱(XPro)。自然殺傷細胞激活平台包括開發的INKmune,用於激活患者的Nk細胞,以消除患有癌症的患者中的微小殘留疾病。inmune bio的產品平台採用精準醫學方法治療各種血液學和實體瘤惡性腫瘤以及慢性炎症。要了解更多信息,請訪問。

Forward Looking Statements

前瞻性聲明

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.

臨床試驗處於早期階段,不能保證實現任何具體的結果。本新聞稿中包含的任何不描述歷史事實的聲明可能構成前瞻性聲明,如1995年《私人證券訴訟改革法》中所定義。本新聞稿中包含的任何不描述歷史事實的聲明可能構成前瞻性聲明,如1995年《私人證券訴訟改革法》中所定義。任何此類前瞻性聲明均基於目前的期望,但由於這些風險和不確定性的存在,實際結果和某些事件和情況的時間可能因這些風險和不確定性而有所不同。 INB03、XPro1595(XPro)和INKmune仍處於臨床試驗階段或正在準備開始臨床試驗,尚未獲得美國食品和藥物管理局(FDA)或任何監管機構的批准,不能確保將獲得FDA或任何監管機構的批准或實現任何具體的結果。可能導致實際未來結果有所不同的因素有很多,但不限於,與公司爲臨床試驗生產更多藥物的能力有關的風險和不確定性; 爲了繼續其業務並進行研究和開發、臨床研究和未來產品商業化活動所需的大量額外資金的可用性; 以及公司的業務、研究、產品開發、監管批准、市場營銷和分銷計劃和策略。這些和其他因素在公司提交給證券和交易委員會的文件中有更詳細的描述,包括公司的年度報告提交的10-k,公司提交的季度報告提交的10-Q以及公司提交的當前報告提交的8-k。公司假定沒有任何義務更新任何前瞻性聲明以反映可能在本發行日期之後出現的任何事件或情況。

For OmniScience:

對於OmniScience:

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

媒體聯繫:
Sean Leous
ICR 醫療保健
Sean.leous@icrhealthcare.com
646-866-4012

For INmune Bio Inc.:

對於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
聯合創始人和致富金融(臨時代碼)官員
(858)964-3720
info@inmunebio.com

丹尼爾·卡爾森
投資者關係主管
(415) 509-4590
dcarlson@inmunebio.com

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

投資者聯繫人:
邁克·莫迪爾
董事總經理 – LifeSci Advisors
mmoyer@lifesciadvisors.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。
    搶先評論

    聲明

    本頁的譯文內容由軟件翻譯。富途將竭力但卻不能保證翻譯內容之準確和可靠,亦不會承擔因任何不準確或遺漏而引起的任何損失或損害。