Bolt Biotherapeutics Reports Q2 Financial Results, Cash Balance of $48.5mln
PorAinvest
jueves, 14 de agosto de 2025, 9:11 pm ET1 min de lectura
BOLT--
Q2 financial highlights include collaboration revenue of $1.8 million, reduced R&D expenses of $7.5 million (down from $15.4M in Q2 2024), and G&A expenses of $3.5 million (down from $4.9M). The company completed a 1:20 reverse stock split on June 6, 2025, regaining Nasdaq compliance. Bolt continues collaborations with Genmab and Toray while seeking a partner for BDC-3042, which showed partial response in lung cancer patients.
Bolt Biotherapeutics' Q2 results paint a picture of a biotech in transition, working to advance its lead candidate while managing a limited cash runway. The company's focus has shifted to BDC-4182, a next-generation claudin 18.2 ISAC now in Phase 1 for gastric and gastroesophageal cancers. This represents a pivot after discontinuing development of trastuzumab imbotolimod (formerly BDC-1001) in May 2024.
The financial position shows both challenges and prudent management. With $48.5 million in cash as of June 30, Bolt projects runway through mid-2026, which should cover initial data readouts from the BDC-4182 trial expected in H1 2026. However, this represents a relatively tight timeline for a clinical-stage biotech with multiple programs.
The 88% reduction in quarterly operating loss (from $22.6 million to $9.2 million year-over-year) demonstrates successful cost-cutting measures, including a significant restructuring in May 2024. R&D expenses decreased by 51% to $7.5 million, while G&A expenses dropped by 29% to $3.5 million.
Importantly, Bolt is seeking a partner for BDC-3042 (dectin-2 agonist antibody) after completing dose escalation, with early signs of efficacy including a partial response in lung cancer at the highest dose. The company also maintains collaborations with Genmab and Toray, which generated $1.8 million in revenue this quarter, up from $1.3 million in Q2 2024.
The 1:20 reverse stock split implemented in June 2025 helped Bolt regain Nasdaq compliance, avoiding a potential delisting scenario. This financial engineering, while necessary, signals the challenges the company has faced in maintaining investor confidence.
References:
[1] https://www.stocktitan.net/news/BOLT/bolt-biotherapeutics-reports-second-quarter-2025-financial-results-huqt80ia0u65.html
[2] https://www.globenewswire.com/news-release/2025/08/14/3133839/0/en/Bolt-Biotherapeutics-Reports-Second-Quarter-2025-Financial-Results-and-Provides-Business-Update.html
• Bolt Biotherapeutics reported Q2 2025 financial results. • BDC-4182, a next-gen Boltbody ISAC, is in Phase 1 dose-escalation study. • Cash balance is $48.5 million as of June 30, 2025, funding through mid-2026. • Focus on advancing BDC-4182 in gastric and gastroesophageal junction cancers.
Redwood City, Calif., Aug. 14, 2025 (GLOBE NEWSWIRE) – Bolt Biotherapeutics (Nasdaq: BOLT), a clinical-stage biopharmaceutical company developing novel immunotherapies for the treatment of cancer, today reported financial results for the second quarter ended June 30, 2025, and provided a business update. The company's lead candidate, BDC-4182, a next-generation claudin 18.2 ISAC, has entered Phase 1 dose-escalation studies for gastric and gastroesophageal cancer. The company reported $48.5 million in cash as of June 30, 2025, expected to fund operations through mid-2026.Q2 financial highlights include collaboration revenue of $1.8 million, reduced R&D expenses of $7.5 million (down from $15.4M in Q2 2024), and G&A expenses of $3.5 million (down from $4.9M). The company completed a 1:20 reverse stock split on June 6, 2025, regaining Nasdaq compliance. Bolt continues collaborations with Genmab and Toray while seeking a partner for BDC-3042, which showed partial response in lung cancer patients.
Bolt Biotherapeutics' Q2 results paint a picture of a biotech in transition, working to advance its lead candidate while managing a limited cash runway. The company's focus has shifted to BDC-4182, a next-generation claudin 18.2 ISAC now in Phase 1 for gastric and gastroesophageal cancers. This represents a pivot after discontinuing development of trastuzumab imbotolimod (formerly BDC-1001) in May 2024.
The financial position shows both challenges and prudent management. With $48.5 million in cash as of June 30, Bolt projects runway through mid-2026, which should cover initial data readouts from the BDC-4182 trial expected in H1 2026. However, this represents a relatively tight timeline for a clinical-stage biotech with multiple programs.
The 88% reduction in quarterly operating loss (from $22.6 million to $9.2 million year-over-year) demonstrates successful cost-cutting measures, including a significant restructuring in May 2024. R&D expenses decreased by 51% to $7.5 million, while G&A expenses dropped by 29% to $3.5 million.
Importantly, Bolt is seeking a partner for BDC-3042 (dectin-2 agonist antibody) after completing dose escalation, with early signs of efficacy including a partial response in lung cancer at the highest dose. The company also maintains collaborations with Genmab and Toray, which generated $1.8 million in revenue this quarter, up from $1.3 million in Q2 2024.
The 1:20 reverse stock split implemented in June 2025 helped Bolt regain Nasdaq compliance, avoiding a potential delisting scenario. This financial engineering, while necessary, signals the challenges the company has faced in maintaining investor confidence.
References:
[1] https://www.stocktitan.net/news/BOLT/bolt-biotherapeutics-reports-second-quarter-2025-financial-results-huqt80ia0u65.html
[2] https://www.globenewswire.com/news-release/2025/08/14/3133839/0/en/Bolt-Biotherapeutics-Reports-Second-Quarter-2025-Financial-Results-and-Provides-Business-Update.html
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