Allogene Q2 Cash Tops $300 Million: A Strategic Inflection Point
PorAinvest
viernes, 15 de agosto de 2025, 1:49 am ET2 min de lectura
ALLO--
Key highlights from the quarter include significant progress in the ALPHA3 trial, the initiation of the ALLO-329 autoimmune study, and the advancement of the ALLO-316 solid tumor program. The ALPHA3 trial, which is evaluating cemacabtagene ansegedleucel (Cema-Cel) in first-line consolidation in large B-cell lymphoma (LBCL), has been streamlined to proceed as a randomized study with two arms, comparing Cema-Cel after standard fludarabine and cyclophosphamide (FC) lymphodepletion to observation [1]. This trial is expected to provide MRD conversion rates between the two arms in the first half of 2026 [1].
The ALLO-329 study, which launched in the second quarter of 2025, is a Phase 1 RESOLUTION basket trial in rheumatology, evaluating CAR T therapy across multiple autoimmune conditions [1]. This trial features two lymphodepletion arms and aims to provide biomarker and proof-of-concept data in the first half of 2026 [1]. The ALLO-316 trial, which is the only allogeneic CAR T therapy to show potential in solid tumors, has completed enrollment in its Phase 1b cohort and presented updated data at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting [1]. The company has met with the FDA to align on the design of a pivotal trial for ALLO-316, laying the groundwork for potential partnership discussions [1].
Research and development expenses for the second quarter of 2025 totaled $40.2 million, while general and administrative expenses amounted to $14.3 million [1]. The company expects an expected decrease in cash, cash equivalents, and investments of approximately $150 million for 2025 and GAAP operating expenses of approximately $230 million, including estimated non-cash stock-based compensation expense of approximately $45 million [1].
Allogene Therapeutics will host a live conference call and webcast today at 2:00 p.m. PT / 5:00 p.m. ET to discuss financial results and provide a business update [1]. The listen-only webcast will be available on the Company's website at www.allogene.com under the Investors tab in the News and Events section [1].
References:
[1] Allogene Therapeutics, Inc. (2025). Allogene Therapeutics Reports Second Quarter 2025 Financial Results and Strategic Advancements. Retrieved from https://ir.allogene.com/news-releases/news-release-details/allogene-therapeutics-reports-second-quarter-2025-financial
Allogene Therapeutics reported Q2 2025 results with $302.6 million in cash and investments, a GAAP net loss of $50.9 million, and a projected cash runway into H2 2027. The company streamlined the ALPHA-three trial, advanced the ALLO-316 solid tumor program, and initiated the ALLO-329 autoimmune study. These developments signal critical strategic inflection points for its allogeneic CAR T cell pipeline, positioning Allogene as a leader in the nascent allogeneic CAR T solid tumor domain.
Allogene Therapeutics, Inc. (Nasdaq: ALLO), a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T™) products for cancer and autoimmune disease, reported its second-quarter 2025 financial results and strategic advancements. The company announced a cash balance of $302.6 million, a GAAP net loss of $50.9 million, and a projected cash runway extending into the second half of 2027 [1].Key highlights from the quarter include significant progress in the ALPHA3 trial, the initiation of the ALLO-329 autoimmune study, and the advancement of the ALLO-316 solid tumor program. The ALPHA3 trial, which is evaluating cemacabtagene ansegedleucel (Cema-Cel) in first-line consolidation in large B-cell lymphoma (LBCL), has been streamlined to proceed as a randomized study with two arms, comparing Cema-Cel after standard fludarabine and cyclophosphamide (FC) lymphodepletion to observation [1]. This trial is expected to provide MRD conversion rates between the two arms in the first half of 2026 [1].
The ALLO-329 study, which launched in the second quarter of 2025, is a Phase 1 RESOLUTION basket trial in rheumatology, evaluating CAR T therapy across multiple autoimmune conditions [1]. This trial features two lymphodepletion arms and aims to provide biomarker and proof-of-concept data in the first half of 2026 [1]. The ALLO-316 trial, which is the only allogeneic CAR T therapy to show potential in solid tumors, has completed enrollment in its Phase 1b cohort and presented updated data at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting [1]. The company has met with the FDA to align on the design of a pivotal trial for ALLO-316, laying the groundwork for potential partnership discussions [1].
Research and development expenses for the second quarter of 2025 totaled $40.2 million, while general and administrative expenses amounted to $14.3 million [1]. The company expects an expected decrease in cash, cash equivalents, and investments of approximately $150 million for 2025 and GAAP operating expenses of approximately $230 million, including estimated non-cash stock-based compensation expense of approximately $45 million [1].
Allogene Therapeutics will host a live conference call and webcast today at 2:00 p.m. PT / 5:00 p.m. ET to discuss financial results and provide a business update [1]. The listen-only webcast will be available on the Company's website at www.allogene.com under the Investors tab in the News and Events section [1].
References:
[1] Allogene Therapeutics, Inc. (2025). Allogene Therapeutics Reports Second Quarter 2025 Financial Results and Strategic Advancements. Retrieved from https://ir.allogene.com/news-releases/news-release-details/allogene-therapeutics-reports-second-quarter-2025-financial

Divulgación editorial y transparencia de la IA: Ainvest News utiliza tecnología avanzada de Modelos de Lenguaje Largo (LLM) para sintetizar y analizar datos de mercado en tiempo real. Para garantizar los más altos estándares de integridad, cada artículo se somete a un riguroso proceso de verificación con participación humana.
Mientras la IA asiste en el procesamiento de datos y la redacción inicial, un miembro editorial profesional de Ainvest revisa, verifica y aprueba de forma independiente todo el contenido para garantizar su precisión y cumplimiento con los estándares editoriales de Ainvest Fintech Inc. Esta supervisión humana está diseñada para mitigar las alucinaciones de la IA y garantizar el contexto financiero.
Advertencia sobre inversiones: Este contenido se proporciona únicamente con fines informativos y no constituye asesoramiento profesional de inversión, legal o financiero. Los mercados conllevan riesgos inherentes. Se recomienda a los usuarios que realicen una investigación independiente o consulten a un asesor financiero certificado antes de tomar cualquier decisión. Ainvest Fintech Inc. se exime de toda responsabilidad por las acciones tomadas con base en esta información. ¿Encontró un error? Reportar un problema

Comentarios
Aún no hay comentarios