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Cartesian Therapeutics to Present Updated Data from Phase 2b Trial of Descartes-08 in Patients with Myasthenia Gravis at the 2nd Annual Cell Therapy for Autoimmune Disease Summit

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Cartesian Therapeutics (NASDAQ: RNAC) announced it will present updated efficacy and safety data from its Phase 2b trial of Descartes-08 in patients with generalized myasthenia gravis at the 2nd Annual Cell Therapy for Autoimmune Disease Summit in Philadelphia. The presentation, titled 'Perspectives on Bringing Cell Therapies to the Autoimmune Space: From Concept to Clinic,' will be delivered by Chief Medical Officer Miloš Miljković on December 3, 2024. The company will host a conference call and webcast with key opinion leader Dr. James F. Howard Jr. to discuss the updated data and planned Phase 3 trial design.

Cartesian Therapeutics (NASDAQ: RNAC) ha annunciato che presenterà dati aggiornati sull'efficacia e la sicurezza del suo trial di Fase 2b di Descartes-08 in pazienti con miastenia gravis generalizzata durante il 2° Summit Annuale sulle Terapie Cellulari per le Malattie Autoimmuni a Philadelphia. La presentazione, intitolata 'Prospettive sul Trasferimento delle Terapie Cellulari nello Spazio Autoimmune: Dal Concetto alla Clinica', sarà tenuta dal Direttore Medico Miloš Miljković il 3 dicembre 2024. L'azienda sarà inoltre presente con una conferenza telefonica e un webcast con il leader di opinione Dr. James F. Howard Jr. per discutere i dati aggiornati e il design del trial di Fase 3 previsto.

Cartesian Therapeutics (NASDAQ: RNAC) anunció que presentará datos actualizados sobre la eficacia y seguridad de su ensayo de Fase 2b de Descartes-08 en pacientes con miastenia gravis generalizada en la 2ª Cumbre Anual de Terapias Celulares para Enfermedades Autoinmunes en Filadelfia. La presentación, titulada 'Perspectivas sobre la Introducción de Terapias Celulares en el Espacio Autoinmune: Del Concepto a la Clínica', será realizada por el Director Médico Miloš Miljković el 3 de diciembre de 2024. La empresa también llevará a cabo una conferencia telefónica y un webcast con el Dr. James F. Howard Jr., un líder de opinión clave, para discutir los datos actualizados y el diseño del ensayo de Fase 3 planeado.

카르테시안 테라퓨틱스 (NASDAQ: RNAC)는 필라델피아에서 열리는 제2회 자가면역질환 세포치료 서밋에서 Descartes-08의 2b상 시험에 대한 효능 및 안전성 데이터를 업데이트하여 발표할 것이라고 발표했습니다. '자가면역 분야에 세포 치료를 도입하는 관점: 개념에서 클리닉까지'라는 제목의 발표는 Miloš Miljković 최고 의학 책임자가 2024년 12월 3일에 진행할 예정입니다. 회사는 또한 주요 의견 선도자인 Dr. James F. Howard Jr.와 함께 업데이트된 데이터 및 계획된 3상 시험 설계에 대해 논의하기 위해 전화 회의 및 웹캐스트를 개최할 것입니다.

Cartesian Therapeutics (NASDAQ: RNAC) a annoncé qu'il présentera des données d'efficacité et de sécurité mises à jour de son essai de Phase 2b concernant Descartes-08 chez des patients atteints de myasthénie grave généralisée lors du 2ème Sommet Annuel sur la Thérapie Cellulaire pour les Maladies Auto-immunes à Philadelphie. La présentation, intitulée 'Perspectives pour l'Intégration des Thérapies Cellulaires dans le Domaine Auto-immun: Du Concept à la Clinique', sera donnée par le Directeur Médical Miloš Miljković le 3 décembre 2024. L'entreprise organisera également une téléconférence et un webinaire avec le leader d'opinion Dr. James F. Howard Jr. pour discuter des données mises à jour et de la conception de l'essai de Phase 3 prévue.

Cartesian Therapeutics (NASDAQ: RNAC) gab bekannt, dass es aktualisierte Wirksamkeits- und Sicherheitsdaten aus seiner Phase 2b-Studie zu Descartes-08 bei Patienten mit generalisierter Myasthenia gravis auf dem 2. jährlichen Gipfel für Zelltherapien bei Autoimmunerkrankungen in Philadelphia präsentieren wird. Die Präsentation mit dem Titel 'Perspektiven zur Einführung von Zelltherapien im Bereich Autoimmunität: Vom Konzept zur Klinik' wird am 3. Dezember 2024 von Chief Medical Officer Miloš Miljković gehalten. Das Unternehmen wird auch eine Telefonkonferenz und einen Webcast mit dem führenden Meinungsführer Dr. James F. Howard Jr. veranstalten, um die aktualisierten Daten und das geplante Design der Phase-3-Studie zu besprechen.

Positive
  • Company advancing to Phase 3 trial planning stage for Descartes-08
  • Scheduled presentation of Phase 2b trial results at major industry summit
Negative
  • None.

Company to host conference call and webcast with key opinion leader on December 3, 2024, at 7:30 a.m. ET

FREDERICK, Md., Nov. 21, 2024 (GLOBE NEWSWIRE) -- Cartesian Therapeutics, Inc. (NASDAQ: RNAC) (the “Company”), a clinical-stage biotechnology company pioneering mRNA cell therapy for autoimmune diseases, today announced that updated efficacy and safety data from the Phase 2b trial of Descartes-08 in patients with generalized myasthenia gravis will be presented at the 2nd Annual Cell Therapy for Autoimmune Disease Summit, being held December 2-4, 2024 in Philadelphia.

Details of the presentation are as follows:

  • Title: Perspectives on Bringing Cell Therapies to the Autoimmune Space: From Concept to Clinic
  • Session Name: Diving into Challenges & Successes in the Autoimmune Space to Direct Future Outcomes
  • Presenter: Miloš Miljković, M.D., M.Sc., Chief Medical Officer, Cartesian Therapeutics
  • Session Date/Time: Tuesday, December 3, 2024, 9:30-10:00 a.m. ET

Conference Call and Webcast

The Company will host a conference call and webcast to discuss the updated data, as well as details regarding the design of its planned Phase 3 trial, on Tuesday, December 3, 2024, at 7:30 a.m. ET. Joining members of the Cartesian management team will be key opinion leader James F. Howard Jr., M.D., Professor of Neurology, Medicine, and Allied Health at the University of North Carolina School of Medicine.

To access the conference call, please dial 1-800-715-9871 (toll-free) or 1-646-307-1963 (international) at least 10 minutes prior to the start time and ask to be joined into the Cartesian Therapeutics call. The live audio webcast, along with accompanying slides, can be accessed on the Events & Presentations section of Cartesian’s website at https://ir.cartesiantherapeutics.com/news-and-events/events-presentations. A replay of the webcast will be available for a limited time following the event on Cartesian’s website.

About Descartes-08

Descartes-08, Cartesian’s lead mRNA cell therapy candidate, is an autologous mRNA-engineered chimeric antigen receptor T-cell therapy (mRNA CAR-T) product targeting B-cell maturation antigen (BCMA) in clinical development for generalized myasthenia gravis (MG) and systemic lupus erythematosus. In contrast to conventional DNA-based CAR T-cell therapies, mRNA CAR-T administration is designed to not require preconditioning chemotherapy, can be administered in the outpatient setting, and does not carry the risk of genomic integration associated with cancerous transformation. Descartes-08 has been granted Orphan Drug Designation and Regenerative Medicine Advanced Therapy Designation by the U.S. Food and Drug Administration for the treatment of MG, and Rare Pediatric Disease Designation for the treatment of juvenile dermatomyositis.

About Cartesian Therapeutics

Cartesian Therapeutics is a clinical-stage company pioneering mRNA cell therapies for the treatment of autoimmune diseases. The Company’s lead asset, Descartes-08, is an mRNA CAR-T in Phase 2b clinical development for patients with generalized myasthenia gravis and Phase 2 development for systemic lupus erythematosus, with a Phase 2 basket trial planned in additional autoimmune indications. The Company’s clinical-stage pipeline also includes Descartes-15, a next-generation, autologous anti-BCMA mRNA CAR-T. For more information, please visit www.cartesiantherapeutics.com or follow the Company on LinkedIn or X, formerly known as Twitter.

Forward Looking Statements

Any statements in this press release about the future expectations, plans and prospects of the Company, including without limitation, statements regarding observations and data from the myasthenia gravis Phase 2b trial, the ability of the Company’s product candidates to be administered in an outpatient setting or without the need for preconditioning lymphodepleting chemotherapy, the potential of Descartes-08, Descartes-15, or any of the Company’s other product candidates to treat myasthenia gravis, systemic lupus erythematosus, juvenile dermatomyositis, or any other disease, the anticipated timing or the outcome of ongoing and planned clinical trials, studies and data readouts, the anticipated timing or the outcome of the FDA’s review of the Company’s regulatory filings, the Company’s ability to conduct its clinical trials and preclinical studies, the timing or making of any regulatory filings, the novelty of treatment paradigms that the Company is able to develop, the potential of any therapies developed by the Company to fulfill unmet medical needs, and enrollment in the Company’s clinical trials and other statements containing the words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “hypothesize,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “would,” and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including, but not limited to, the following: the uncertainties inherent in the initiation, completion and cost of clinical trials including proof of concept trials, including uncertain outcomes, the availability and timing of data from ongoing and future clinical trials and the results of such trials, whether preliminary results from a particular clinical trial will be predictive of the final results of that trial and whether results of early clinical trials will be indicative of the results of later clinical trials, the ability to predict results of studies performed on human beings based on results of studies performed on non-human subjects, the unproven approach of the Company’s technology, potential delays in enrollment of patients, undesirable side effects of the Company’s product candidates, its reliance on third parties to conduct its clinical trials, the Company’s inability to maintain its existing or future collaborations, licenses or contractual relationships, its inability to protect its proprietary technology and intellectual property, potential delays in regulatory approvals, the availability of funding sufficient for its foreseeable and unforeseeable operating expenses and capital expenditure requirements, the Company’s recurring losses from operations and negative cash flows, substantial fluctuation in the price of the Company’s common stock, risks related to geopolitical conflicts and pandemics and other important factors discussed in the “Risk Factors” section of the Company’s most recent Annual Report on Form 10-K and subsequently filed Quarterly Reports on Form 10-Q, and in other filings that the Company makes with the Securities and Exchange Commission. In addition, any forward-looking statements included in this press release represent the Company’s views only as of the date of its publication and should not be relied upon as representing its views as of any subsequent date. The Company specifically disclaims any intention to update any forward-looking statements included in this press release, except as required by law.

Investor Contact

Blaine Davis
Chief Financial Officer
blaine@cartesiantx.com

Media Contact

David Rosen
Argot Partners
david.rosen@argotpartners.com


FAQ

When will Cartesian Therapeutics (RNAC) present Phase 2b trial data for Descartes-08?

Cartesian Therapeutics will present the data on December 3, 2024, at 9:30 AM ET during the 2nd Annual Cell Therapy for Autoimmune Disease Summit in Philadelphia.

What is the purpose of Cartesian Therapeutics' (RNAC) December 3, 2024 conference call?

The conference call will discuss updated Phase 2b trial data for Descartes-08 and details of the planned Phase 3 trial design, featuring key opinion leader Dr. James F. Howard Jr.

What disease is Cartesian Therapeutics' (RNAC) Descartes-08 treating in clinical trials?

Descartes-08 is being tested for the treatment of generalized myasthenia gravis, an autoimmune disease.

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