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Longeveron® Lomecel-B™ Data in Alzheimer’s Disease Selected for Late Breaking Poster Presentation at the Clinical Trials on Alzheimer’s Disease Conference (CTAD24)

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Longeveron Inc. (NASDAQ: LGVN) announced that its submission on Lomecel-B™ has been selected for a late breaking poster presentation at the 17th Clinical Trials on Alzheimer's Disease Conference (CTAD24) in Madrid, Spain. The presentation, titled 'Lomecel-B inhibition of MMP14 activity predicts Lomecel-B bioactivity in the treatment of mild Alzheimer's disease', will be held on October 29-30, 2024.

CEO Wa'el Hashad expressed excitement about presenting important Lomecel-B™ data at this leading Alzheimer's research forum, stating that the findings offer potential mechanistic and clinical insights for developing cellular-based therapy for Alzheimer's disease. The abstract will also be included in the special CTAD edition of the Journal of Prevention of Alzheimer's Disease (JPAD), the official journal of the CTAD conference.

Longeveron Inc. (NASDAQ: LGVN) ha annunciato che la sua presentazione su Lomecel-B™ è stata selezionata per una presentazione poster in ritardo alla 17ª Conferenza Clinica sulle Malattie di Alzheimer (CTAD24) a Madrid, Spagna. La presentazione, intitolata 'L'inibizione dell'attività di MMP14 da parte di Lomecel-B predice la bioattività di Lomecel-B nel trattamento della malattia di Alzheimer lieve', si terrà il 29-30 ottobre 2024.

Il CEO Wa'el Hashad ha espresso entusiasmo per la presentazione di importanti dati su Lomecel-B™ in questo forum di ricerca di punta sulle malattie di Alzheimer, affermando che i risultati offrono potenziali intuizioni meccanicistiche e cliniche per lo sviluppo di una terapia cellulare per la malattia di Alzheimer. L'abstract sarà inoltre incluso nell'edizione speciale del CTAD del Journal of Prevention of Alzheimer's Disease (JPAD), la rivista ufficiale della conferenza CTAD.

Longeveron Inc. (NASDAQ: LGVN) anunció que su presentación sobre Lomecel-B™ ha sido seleccionada para una presentación de póster de última hora en la 17ª Conferencia de Ensayos Clínicos sobre la Enfermedad de Alzheimer (CTAD24) en Madrid, España. La presentación, titulada 'La inhibición de la actividad de MMP14 por Lomecel-B predice la bioactividad de Lomecel-B en el tratamiento de la enfermedad de Alzheimer leve', se llevará a cabo el 29 y 30 de octubre de 2024.

El CEO Wa'el Hashad expresó su entusiasmo por presentar datos importantes sobre Lomecel-B™ en este destacado foro de investigación sobre el Alzheimer, afirmando que los hallazgos ofrecen posibles conocimientos mecanicistas y clínicos para el desarrollo de terapia celular para la enfermedad de Alzheimer. El resumen también se incluirá en la edición especial del CTAD del Journal of Prevention of Alzheimer's Disease (JPAD), la revista oficial de la conferencia CTAD.

Longeveron Inc. (NASDAQ: LGVN)는 Lomecel-B™에 대한 제출물이 스페인 마드리드에서 열리는 제17회 알츠하이머병 임상 시험 회의(CTAD24)에서 지연된 포스터 발표로 선정되었다고 발표했습니다. 이 발표의 제목은 'Lomecel-B가 MMP14 활동을 억제하여 경증 알츠하이머병 치료의 Lomecel-B 생리활성을 예측한다'로, 2024년 10월 29일부터 30일까지 진행될 예정입니다.

CEO인 Wa'el Hashad는 이 주요 알츠하이머 연구 포럼에서 중요한 Lomecel-B™ 데이터를 발표하게 되어 매우 기쁘다고 밝혔으며, 이 결과는 알츠하이머병에 대한 세포 기반 치료 개발을 위한 잠재적인 기전적 및 임상적 통찰력을 제공한다고 언급했습니다. 초록은 또한 CTAD 회의의 공식 저널인 Alzheimer’s Disease 예방 저널(JPAD)의 특별 CTAD판에 포함될 것입니다.

Longeveron Inc. (NASDAQ: LGVN) a annoncé que sa soumission concernant Lomecel-B™ a été choisie pour une présentation d'affiche lors de la 17e Conférence sur les essais cliniques sur la maladie d'Alzheimer (CTAD24) à Madrid, en Espagne. La présentation, intitulée 'L'inhibition de l'activité MMP14 par Lomecel-B prédit la bioactivité de Lomecel-B dans le traitement de la maladie d'Alzheimer légère', se tiendra du 29 au 30 octobre 2024.

Le PDG Wa'el Hashad a exprimé son enthousiasme à présenter des données importantes sur Lomecel-B™ dans ce forum de recherche majeur sur la maladie d'Alzheimer, affirmant que les résultats offrent des perspectives mécanistiques et cliniques potentielles pour le développement de thérapies cellulaires contre la maladie d'Alzheimer. Le résumé sera également inclus dans l'édition spéciale du CTAD du Journal of Prevention of Alzheimer's Disease (JPAD), la revue officielle de la conférence CTAD.

Longeveron Inc. (NASDAQ: LGVN) gab bekannt, dass ihre Einreichung zu Lomecel-B™ für eine spontane Poster-Präsentation auf der 17. Konferenz zu klinischen Prüfungen bei Alzheimer-Krankheit (CTAD24) in Madrid, Spanien, ausgewählt wurde. Die Präsentation mit dem Titel 'Die Hemmung der MMP14-Aktivität durch Lomecel-B sagt die Bioaktivität von Lomecel-B bei der Behandlung leichter Alzheimer-Krankheit voraus' findet am 29. und 30. Oktober 2024 statt.

CEO Wa'el Hashad äußerte sich begeistert über die Präsentation wichtiger Lomecel-B™-Daten auf diesem führenden Forschungsforum zur Alzheimer-Krankheit und erklärte, dass die Ergebnisse potenzielle mechanistische und klinische Erkenntnisse für die Entwicklung einer zellulären Therapie bei Alzheimer-Krankheit bieten. Das Abstract wird auch in der speziellen CTAD-Ausgabe des Journal of Prevention of Alzheimer's Disease (JPAD), der offiziellen Zeitschrift der CTAD-Konferenz, veröffentlicht.

Positive
  • Lomecel-B™ data selected for presentation at a major Alzheimer's disease conference
  • Potential insights into cellular-based therapy for Alzheimer's disease
  • Abstract to be published in the Journal of Prevention of Alzheimer's Disease
Negative
  • None.

MIAMI, Oct. 14, 2024 (GLOBE NEWSWIRE) -- Longeveron Inc. (NASDAQ: LGVN), a clinical stage biotechnology company developing regenerative medicines, today announced that its submission entitled “Lomecel-B inhibition of MMP14 activity predicts Lomecel-B bioactivity in the treatment of mild Alzheimer’s disease” has been selected for a late breaking poster presentation at the 17th edition of the Clinical Trials on Alzheimer’s Disease Conference (CTAD24) to be held October 29 -November 1, 2024 in Madrid, Spain.

“We are excited to have been selected to present important Lomecel-B™ data at a leading forum for Alzheimer’s research and clinical investigation,” said Wa’el Hashad, CEO of Longeveron. “We believe the findings offer potential mechanistic and clinical insights in the development of cellular-based therapy for Alzheimer’s disease.”

Late Breaking Poster Presentation

Date: Tuesday, October 29, 2024, 3:00 p.m. CEST to Wednesday, October 30, 5:00 p.m. CEST
Theme: 11. New Therapies and Clinical Trials
Title: LP029 “Lomecel-B inhibition of MMP14 activity predicts Lomecel-B bioactivity in the treatment of mild Alzheimer’s”
 

The abstract of the poster will also be included in the special CTAD edition of the Journal of Prevention of Alzheimer’s Disease (JPAD), the official journal of the CTAD conference.

About Lomecel-B™
Lomecel-B™ is a living cell product made from specialized cells isolated from the bone marrow of young healthy adult donors. These specialized cells, known as medicinal signaling cells (MSCs), are essential to our endogenous biological repair mechanism. MSCs have been shown to perform a number of complex functions in the body, including the formation of new tissue. They also have been shown to respond to sites of injury or disease and secrete bioactive factors that are immunomodulatory and regenerative. We believe that Lomecel-B™ may have multiple potential mechanisms of action that may lead to anti-inflammatory, pro-vascular regenerative responses, and therefore may have broad application for a range of rare and aging related diseases.

About Longeveron Inc.

Longeveron is a clinical stage biotechnology company developing regenerative medicines to address unmet medical needs. The Company’s lead investigational product is Lomecel-B™, an allogeneic medicinal signaling cell (MSC) therapy product isolated from the bone marrow of young, healthy adult donors. Lomecel-B™ has multiple potential mechanisms of action encompassing pro-vascular, pro-regenerative, anti-inflammatory, and tissue repair and healing effects with broad potential applications across a spectrum of disease areas. Longeveron is currently pursuing three pipeline indications: hypoplastic left heart syndrome (HLHS), Alzheimer’s disease (AD), and Aging-related Frailty. Lomecel-B™ development programs have received five distinct and important U.S. FDA designations: for the HLHS program - Orphan Drug designation, Fast Track designation, and Rare Pediatric Disease designation; and, for the AD program - Regenerative Medicine Advanced Therapy (RMAT) designation and Fast Track designation. For more information, visit www.longeveron.com or follow Longeveron on LinkedIn, X, and Instagram.

Forward-Looking Statements
Certain statements in this press release that are not historical facts are forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, which reflect management’s current expectations, assumptions, and estimates of future operations, performance and economic conditions, and involve risks and uncertainties that could cause actual results to differ materially from those anticipated by the statements made herein. Forward-looking statements are generally identifiable by the use of forward-looking terminology such as “believe,” “expects,” “may,” “looks to,” “will,” “should,” “plan,” “intend,” “on condition,” “target,” “see,” “potential,” “estimates,” “preliminary,” or “anticipates” or the negative thereof or comparable terminology, or by discussion of strategy or goals or other future events, circumstances, or effects and include, but are not limited to, the anticipated use of proceeds from recent offerings. Factors that could cause actual results to differ materially from those expressed or implied in any forward-looking statements in this release include, but are not limited to, market and other conditions, our limited operating history and lack of products approved for commercial sale; adverse global conditions, including macroeconomic uncertainty; inability to raise additional capital necessary to continue as a going concern; our history of losses and inability to achieve profitability going forward; the absence of FDA-approved allogenic, cell-based therapies for Aging-related Frailty, Alzheimer’s disease, or other aging-related conditions, or for HLHS or other cardiac-related indications; ethical and other concerns surrounding the use of stem cell therapy or human tissue; our exposure to product liability claims arising from the use of our product candidates or future products in individuals, for which we may not be able to obtain adequate product liability insurance; the adequacy of our trade secret and patent position to protect our product candidates and their uses: others could compete against us more directly, which could harm our business and have a material adverse effect on our business, financial condition, and results of operations; if certain license agreements are terminated, our ability to continue clinical trials and commercially market products could be adversely affected; the inability to protect the confidentiality of our proprietary information, trade secrets, and know-how; third-party claims of intellectual property infringement may prevent or delay our product development efforts; intellectual property rights do not necessarily address all potential threats to our competitive advantage; the inability to successfully develop and commercialize our product candidates and obtain the necessary regulatory approvals; we cannot market and sell our product candidates in the U.S. or in other countries if we fail to obtain the necessary regulatory approvals; final marketing approval of our product candidates by the FDA or other regulatory authorities for commercial use may be delayed, limited, or denied, any of which could adversely affect our ability to generate operating revenues; we may not be able to secure and maintain research institutions to conduct our clinical trials; ongoing healthcare legislative and regulatory reform measures may have a material adverse effect on our business and results of operations; if we receive regulatory approval of Lomecel-B™ or any of our other product candidates, we will be subject to ongoing regulatory requirements and continued regulatory review, which may result in significant additional expense; being subject to penalties if we fail to comply with regulatory requirements or experience unanticipated problems with our therapeutic candidates; reliance on third parties to conduct certain aspects of our preclinical studies and clinical trials; interim, “topline” and preliminary data from our clinical trials that we announce or publish from time to time may change as more data become available and are subject to audit and verification procedures that could result in material changes in the final data; the volatility of the price of our Class A common stock; we could lose our listing on the Nasdaq Capital Market; provisions in our certificate of incorporation and bylaws and Delaware law might discourage, delay or prevent a change in control of our company or changes in our management and, therefore, depress the market price of our Class A common stock; we have never commercialized a product candidate before and may lack the necessary expertise, personnel and resources to successfully commercialize any products on our own or together with suitable collaborators; and in order to successfully implement our plans and strategies, we will need to grow our organization, and we may experience difficulties in managing this growth. Further information relating to factors that may impact the Company’s results and forward-looking statements are disclosed in the Company’s filings with the Securities and Exchange Commission, including Longeveron’s Annual Report on Form 10-K for the year ended December 31, 2023, filed with the Securities and Exchange Commission on February 27, 2024, as amended by the Annual Report on Form 10-K/A filed March 11, 2024, its Quarterly Reports on Form 10-Q, and its Current Reports on Form 8-K. The forward-looking statements contained in this press release are made as of the date of this press release, and the Company disclaims any intention or obligation, other than imposed by law, to update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise.

Investor and Media Contact:
Derek Cole
Investor Relations Advisory Solutions
derek.cole@iradvisory.com

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/cfb4911d-2b0b-4c52-b2fa-b6982947155d


FAQ

What is the title of Longeveron's presentation at CTAD24?

Longeveron's presentation at CTAD24 is titled 'Lomecel-B inhibition of MMP14 activity predicts Lomecel-B bioactivity in the treatment of mild Alzheimer's disease'.

When and where will Longeveron (LGVN) present its Lomecel-B data?

Longeveron (LGVN) will present its Lomecel-B data at the Clinical Trials on Alzheimer's Disease Conference (CTAD24) in Madrid, Spain, from October 29 to November 1, 2024.

What potential benefits does Longeveron's Lomecel-B offer for Alzheimer's treatment?

According to Longeveron's CEO, the Lomecel-B findings offer potential mechanistic and clinical insights in the development of cellular-based therapy for Alzheimer's disease.

Will Longeveron's (LGVN) research be published in a scientific journal?

Yes, the abstract of Longeveron's (LGVN) poster presentation will be included in the special CTAD edition of the Journal of Prevention of Alzheimer's Disease (JPAD).

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