Join Calidi Biotherapeutics’ Exclusive Live Investor Webinar and Q&A Session on July 24
Calidi Biotherapeutics (NYSE American: CLDI) will host an investor webinar on July 24, 2025, at 4:15 p.m. ET featuring CEO Eric Poma. The presentation will highlight their RedTail™ platform, an engineered viral therapy system designed to deliver genetic medicines to metastatic tumors.
The company's lead candidate, CLD-401, has shown promising preclinical results at AACR and ASCO, demonstrating tumor elimination and immune memory development. The targeted oncology market is projected to reach $560 billion by 2033. Calidi is progressing toward IND filing while seeking strategic pharma partnerships for global commercialization.
Calidi Biotherapeutics (NYSE American: CLDI) terrà un webinar per investitori il 24 luglio 2025 alle 16:15 ET, con la partecipazione del CEO Eric Poma. La presentazione metterà in luce la loro piattaforma RedTail™, un sistema di terapia virale ingegnerizzato progettato per veicolare medicinali genetici ai tumori metastatici.
Il candidato principale dell'azienda, CLD-401, ha mostrato risultati preclinici promettenti durante AACR e ASCO, dimostrando l'eliminazione del tumore e lo sviluppo della memoria immunitaria. Il mercato oncologico mirato è previsto raggiungere 560 miliardi di dollari entro il 2033. Calidi sta avanzando verso la presentazione dell'IND mentre cerca partnership strategiche con aziende farmaceutiche per la commercializzazione globale.
Calidi Biotherapeutics (NYSE American: CLDI) realizará un seminario web para inversores el 24 de julio de 2025 a las 4:15 p.m. ET, con la participación del CEO Eric Poma. La presentación destacará su plataforma RedTail™, un sistema de terapia viral diseñado para entregar medicamentos genéticos a tumores metastásicos.
El candidato principal de la compañía, CLD-401, ha mostrado resultados preclínicos prometedores en AACR y ASCO, demostrando la eliminación del tumor y el desarrollo de memoria inmunológica. Se proyecta que el mercado oncológico dirigido alcance 560 mil millones de dólares para 2033. Calidi avanza hacia la presentación del IND mientras busca asociaciones estratégicas con farmacéuticas para la comercialización global.
Calidi Biotherapeutics (NYSE American: CLDI)는 2025년 7월 24일 오후 4시 15분 ET에 CEO Eric Poma가 참여하는 투자자 웨비나를 개최할 예정입니다. 이번 발표에서는 전이성 종양에 유전자 약물을 전달하기 위해 설계된 바이러스 치료 시스템인 RedTail™ 플랫폼을 소개합니다.
회사의 주요 후보물질인 CLD-401은 AACR 및 ASCO에서 종양 제거 및 면역 기억 형성을 입증하는 유망한 전임상 결과를 보였습니다. 표적 암 시장은 2033년까지 5600억 달러에 이를 것으로 예상됩니다. Calidi는 IND 제출을 진행 중이며, 글로벌 상용화를 위한 전략적 제약 파트너십을 모색하고 있습니다.
Calidi Biotherapeutics (NYSE American : CLDI) organisera un webinaire pour investisseurs le 24 juillet 2025 à 16h15 ET, avec la participation du PDG Eric Poma. La présentation mettra en avant leur plateforme RedTail™, un système de thérapie virale conçu pour délivrer des médicaments génétiques aux tumeurs métastatiques.
Le candidat principal de la société, CLD-401, a présenté des résultats précliniques prometteurs lors des conférences AACR et ASCO, démontrant l’élimination des tumeurs et le développement de la mémoire immunitaire. Le marché ciblé de l’oncologie devrait atteindre 560 milliards de dollars d’ici 2033. Calidi progresse vers le dépôt d’une demande d’IND tout en recherchant des partenariats stratégiques avec des laboratoires pharmaceutiques pour une commercialisation mondiale.
Calidi Biotherapeutics (NYSE American: CLDI) veranstaltet am 24. Juli 2025 um 16:15 Uhr ET ein Webinar für Investoren mit CEO Eric Poma. Die Präsentation stellt ihre RedTail™-Plattform vor, ein entwickeltes virales Therapiesystem zur gezielten Abgabe genetischer Medikamente an metastasierende Tumore.
Der führende Kandidat des Unternehmens, CLD-401, zeigte bei AACR und ASCO vielversprechende präklinische Ergebnisse mit Tumoreliminierung und Entwicklung immunologischen Gedächtnisses. Der adressierbare Onkologiemarkt wird bis 2033 voraussichtlich 560 Milliarden US-Dollar erreichen. Calidi arbeitet auf die IND-Einreichung hin und sucht strategische Pharma-Partnerschaften für die globale Vermarktung.
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SAN DIEGO, July 22, 2025 (GLOBE NEWSWIRE) -- Calidi Biotherapeutics, Inc. (“Calidi” or the “Company”) (NYSE American: CLDI), a clinical-stage biotechnology company pioneering the development of targeted therapies with the potential to deliver genetic medicines to distal sites of disease, is pleased to invite investors to a webinar on July 24, 2025, at 4:15 p.m. ET.
The exclusive event, hosted by RedChip Companies, will feature Calidi’s CEO, Eric Poma, Ph.D. Attendees will gain insights into Calidi’s pioneering approach to precision genetic medicine, enabled by its proprietary RedTail™ platform—an engineered, systemically delivered viral therapy designed to reach metastatic and difficult-to-treat tumors. The platform cloaks potent genetic payloads, such as IL-15 superagonist, within a human-derived envelope, allowing the virus to evade immune detection and circulate throughout the body. Preclinical data showcased at AACR and ASCO demonstrated that a single dose of Calidi’s lead candidate, CLD-401, not only eliminated metastatic tumors but also primed immune memory, offering the potential to prevent recurrence. With its scalable, non-integrating viral backbone and ability to deliver multiple genetic payloads, RedTail positions Calidi to address a vast oncology market projected to exceed
A live question and answer session will follow the presentation.
To register for the free webinar, please visit: https://www.redchip.com/webinar/CLDI/83183638975
Questions can be pre-submitted to CLDI@redchip.com or online during the live event.
About Calidi Biotherapeutics
Calidi Biotherapeutics (NYSE American: CLDI) is a clinical-stage biotechnology company pioneering the development of targeted therapies that can deliver genetic medicines to sites of disease. The company's proprietary Redtail platform represents a decade of development and expertise in designing viral vectors that can evade immune detection allowing for systemic delivery and distal sites of disease in oncology and, potentially, other indications. This advanced enveloped technology is intended to shield the virus from immune clearance, allowing virotherapy to effectively reach tumor sites, induce tumor lysis, and deliver potent gene therapies to metastatic locations.
The lead candidate from the Redtail platform, currently in IND-enabling studies, targets non-small cell lung cancer, ovarian cancer, and other tumor types with high unmet medical need. Additionally, Calidi is developing protected virotherapies, in clinical-stage, for intratumoral and localized administration, focusing on a subset of injectable cancer indications.
Calidi Biotherapeutics is headquartered in San Diego, California. For more information, please visit www.calidibio.com.
Forward-Looking Statements
This press release may contain forward-looking statements for purposes of the “safe harbor” provisions under the United States Private Securities Litigation Reform Act of 1995. Terms such as “anticipates,” “believe,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible,” “potential,” “predicts,” “project,” “should,” “towards,” “would” as well as similar terms, are forward-looking in nature, but the absence of these words does not mean that a statement is not forward-looking. These forward looking statements include, but are not limited to, statements concerning use of proceeds from the offering, that the closing of offering will occur or will occur on the anticipated closing date, upcoming key milestones, planned clinical trials, and statements relating to the safety and efficacy of Calidi’s therapeutic candidates in development. Any forward-looking statements contained in this discussion are based on Calidi’s current expectations and beliefs concerning future developments and their potential effects and are subject to multiple risks and uncertainties that could cause actual results to differ materially and adversely from those set forth or implied in such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that Calidi is not able to raise sufficient capital to support its current and anticipated clinical trials, the risk that early results of clinical trials do not necessarily predict final results and that one or more of the clinical outcomes may materially change following more comprehensive review of the data, and as more patient data becomes available, the risk that Calidi may not receive FDA approval for some or all of its therapeutic candidates. Other risks and uncertainties are set forth in the section entitled “Risk Factors” and “Cautionary Note Regarding Forward-Looking Statements” in the Company’s Form 10-K filed on March 31, 2025 and Form 10-Q filed on May 14, 2025. These reports may be amended or supplemented by other reports we file with the SEC from time to time.
Contact:
Dave Gentry
RedChip Companies, Inc.
1-407-644-4256
CLDI@redchip.com
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