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NEC Announces Interim Results from Phase 1 Clinical Trial of NECVAX-NEO1, an AI-Driven Personalized Oral Cancer Vaccine, at ESMO Immuno-Oncology Congress 2024 By Investing.com
TOKYO, Dec 12, 2024 - (JCN Newswire) - - NEC Bio Therapeutics today presents 24-week promising interim results from an ongoing Phase 1 basket clinical trial of an orally administered cancer vaccine, NECVAX-NEO1, used in combination with checkpoint inhibitors (CPI) for treating patients with solid tumors. The findings are being presented in a poster at the ESMO Immuno-Oncology Congress in Geneva, Switzerland from December 11 to 13, 2024. NECVAX-NEO1 is a personalized bacteria-based oral DNA therapeutic vaccine, developed using AI prediction of the most immunogenic patient-specific neoepitopes. This vaccine is designed to activate the patient's immune system, prompting a T-cell response that can precisely target and eliminate tumor cells based on the individual's unique neoantigens. In the phase 1 study, 5 patients with melanoma, renal cell cancer, or head and neck cancer, who have been on CPI treatment for at least three months, were treated with NECVAX-NEO1. The safety run-in phase showed no treatment-related toxicities, allowing a dose increase. An ELISPOT response was induced by 68% of neoepitopes, with 40% of patients showing significant neoantigen-specific signals. After a 24-week treatment period, 80% of patients had a stable disease status, indicating a high disease control rate. On the results of the clinical study, Dr. Heinz Lubenau, CEO of NEC Bio Therapeutics, commented, "We are very excited about our first proof-of-concept data showing signs of promising immunogenicity and associated biomarker changes in patients. This is very encouraging, especially in light of new clinical trials currently ongoing at various locations in early and late-stage cancer patients. We are looking forward to generating more data for NECVAX-NEO1 as an additional treatment option for patients with difficult to treat cancer in the future." Motoo Nishihara, Corporate Executive Vice President and CTO of NEC Corporation, further commented, "We are certainly excited to present the progress of the NECVAX-NEO1 trial demonstrating safety and signs of immunogenicity. NECVAX-NEO1 is the first cancer vaccine asset to be clinically developed at NEC. This development ties in with the larger NEC mission of providing healthcare solutions globally using the state of art technologies developed in-house." Details of the poster are below: Poster title: Oral DNA vaccination targeting personalised neoantigens in immune checkpoint inhibitor treated solid tumor patients - Interim results. Authors: Domas Vaitiekus, E. Juozaityte, L. Puzauskienė, S. Tulyte, L. Gatijatullin, M. Platten, I. Poschke, I.Hulsmeyer, A. Kuhn, A. Aranguren, H. Lubenau, H. Fontenelle, B. Simovski, Y. Yamashita, C.Chaput, A. Meiser, V. Urbonas The poster may also be found here: Link to NEC Bio website. Trial details can also be viewed at: NCT05354323 NECVAX-NEO1 is currently under evaluation at additional clinical trial sites in Lithuania, Germany, and Spain. These sites are actively recruiting patients and are open for enrollment. About NEC Bio Therapeutics NEC Bio Therapeutics, established in Mannheim, Germany, focuses on the clinical strategy and development, as well as planning and execution of clinical trials in the oncology area. It is a subsidiary of NEC Bio, the biotech arm of NEC Corporation. NEC Bio is located in the Netherlands and dedicated to the development of innovative biotechnological solutions to tackle some of the most pressing health challenges. NEC Bio's research and development efforts are focused on creating personalized therapies that improve the quality of life for patients worldwide. NEC OncoImmunity in Oslo, Norway, is also a subsidiary of NEC Bio. For more information, visit: www.nec-bio.com About NEC Corporation NEC Corporation has established itself as a leader in the integration of IT and network technologies while promoting the brand statement of "Orchestrating a brighter world." NEC enables businesses and communities to adapt to rapid changes taking place in both society and the market as it provides for the social values of safety, security, fairness and efficiency to promote a more sustainable world where everyone has the chance to reach their full potential. For more information, visit NEC at https://www.nec.com.
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NEC Announces Interim Results from Phase 1 Clinical Trial of NECVAX-NEO1, an AI-Driven Personalized Oral Cancer Vaccine, at ESMO Immuno-Oncology Congress 2024
Interim results from an ongoing clinical trial of NECVAX-NEO1 highlight its safety and immunogenicity. These results are NEC's first proof-of-concept for an investigational oral DNA vaccine administered in patients with solid tumors. TOKYO, Dec 12, 2024 - (JCN Newswire) - NEC Bio Therapeutics today presents 24-week promising interim results from an ongoing Phase 1 basket clinical trial of an orally administered cancer vaccine, NECVAX-NEO1, used in combination with checkpoint inhibitors (CPI) for treating patients with solid tumors. The findings are being presented in a poster at the ESMO Immuno-Oncology Congress in Geneva, Switzerland from December 11 to 13, 2024. NECVAX-NEO1 is a personalized bacteria-based oral DNA therapeutic vaccine, developed using AI prediction of the most immunogenic patient-specific neoepitopes. This vaccine is designed to activate the patient's immune system, prompting a T-cell response that can precisely target and eliminate tumor cells based on the individual's unique neoantigens. In the phase 1 study, 5 patients with melanoma, renal cell cancer, or head and neck cancer, who have been on CPI treatment for at least three months, were treated with NECVAX-NEO1. The safety run-in phase showed no treatment-related toxicities, allowing a dose increase. An ELISPOT response was induced by 68% of neoepitopes, with 40% of patients showing significant neoantigen-specific signals. After a 24-week treatment period, 80% of patients had a stable disease status, indicating a high disease control rate. On the results of the clinical study, Dr. Heinz Lubenau, CEO of NEC Bio Therapeutics, commented, "We are very excited about our first proof-of-concept data showing signs of promising immunogenicity and associated biomarker changes in patients. This is very encouraging, especially in light of new clinical trials currently ongoing at various locations in early and late-stage cancer patients. We are looking forward to generating more data for NECVAX-NEO1 as an additional treatment option for patients with difficult to treat cancer in the future." Motoo Nishihara, Corporate Executive Vice President and CTO of NEC Corporation, further commented, "We are certainly excited to present the progress of the NECVAX-NEO1 trial demonstrating safety and signs of immunogenicity. NECVAX-NEO1 is the first cancer vaccine asset to be clinically developed at NEC. This development ties in with the larger NEC mission of providing healthcare solutions globally using the state of art technologies developed in-house." Details of the poster are below: Poster title: Oral DNA vaccination targeting personalised neoantigens in immune checkpoint inhibitor treated solid tumor patients - Interim results. Authors: Domas Vaitiekus, E. Juozaityte, L. Puzauskienė, S. Tulyte, L. Gatijatullin, M. Platten, I. Poschke, I.Hulsmeyer, A. Kuhn, A. Aranguren, H. Lubenau, H. Fontenelle, B. Simovski, Y. Yamashita, C.Chaput, A. Meiser, V. Urbonas Poster Number: 160P Date: 12 December 2024 The poster may also be found here: Link to NEC Bio website. Trial details can also be viewed at: NCT05354323 NECVAX-NEO1 is currently under evaluation at additional clinical trial sites in Lithuania, Germany, and Spain. These sites are actively recruiting patients and are open for enrollment. About NEC Bio Therapeutics NEC Bio Therapeutics, established in Mannheim, Germany, focuses on the clinical strategy and development, as well as planning and execution of clinical trials in the oncology area. It is a subsidiary of NEC Bio, the biotech arm of NEC Corporation. NEC Bio is located in the Netherlands and dedicated to the development of innovative biotechnological solutions to tackle some of the most pressing health challenges. NEC Bio's research and development efforts are focused on creating personalized therapies that improve the quality of life for patients worldwide. NEC OncoImmunity in Oslo, Norway, is also a subsidiary of NEC Bio. For more information, visit: www.nec-bio.com About NEC Corporation NEC Corporation has established itself as a leader in the integration of IT and network technologies while promoting the brand statement of "Orchestrating a brighter world." NEC enables businesses and communities to adapt to rapid changes taking place in both society and the market as it provides for the social values of safety, security, fairness and efficiency to promote a more sustainable world where everyone has the chance to reach their full potential. For more information, visit NEC at https://www.nec.com. Source: NEC Corporation Copyright 2024 JCN Newswire . All rights reserved. Market News and Data brought to you by Benzinga APIs
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NEC Bio Therapeutics announces encouraging interim results from a Phase 1 clinical trial of NECVAX-NEO1, an AI-driven personalized oral cancer vaccine, at the ESMO Immuno-Oncology Congress 2024. The vaccine shows promising safety and immunogenicity in patients with solid tumors.
NEC Bio Therapeutics, a subsidiary of NEC Corporation, has unveiled promising interim results from its ongoing Phase 1 clinical trial of NECVAX-NEO1, an innovative AI-driven personalized oral cancer vaccine. The findings were presented at the ESMO Immuno-Oncology Congress 2024 in Geneva, Switzerland, marking a significant milestone in the field of personalized cancer immunotherapy 12.
NECVAX-NEO1 represents a cutting-edge approach to cancer treatment, combining artificial intelligence with personalized medicine. The vaccine is a bacteria-based oral DNA therapeutic, designed using AI to predict the most immunogenic patient-specific neoepitopes. This tailored approach aims to activate the patient's immune system, triggering a precise T-cell response against tumor cells based on the individual's unique neoantigens 12.
The Phase 1 basket trial involved five patients with melanoma, renal cell cancer, or head and neck cancer, who had been receiving checkpoint inhibitor (CPI) treatment for at least three months. Key findings from the 24-week interim results include:
Dr. Heinz Lubenau, CEO of NEC Bio Therapeutics, expressed enthusiasm about the results, stating, "We are very excited about our first proof-of-concept data showing signs of promising immunogenicity and associated biomarker changes in patients." He emphasized the potential of NECVAX-NEO1 as an additional treatment option for patients with difficult-to-treat cancers 12.
Motoo Nishihara, Corporate Executive Vice President and CTO of NEC Corporation, highlighted the significance of NECVAX-NEO1 as NEC's first clinically developed cancer vaccine asset. He noted that this development aligns with NEC's broader mission of providing global healthcare solutions using state-of-the-art technologies 12.
The clinical trial for NECVAX-NEO1 is expanding, with additional sites in Lithuania, Germany, and Spain actively recruiting patients. This expansion aims to generate more comprehensive data on the vaccine's efficacy and safety profile 12.
The poster presentation at the ESMO Immuno-Oncology Congress, titled "Oral DNA vaccination targeting personalised neoantigens in immune checkpoint inhibitor treated solid tumor patients - Interim results," provides detailed insights into the study's methodology and findings 12.
As NEC continues to advance its research in personalized cancer therapies, NECVAX-NEO1 represents a promising step towards more effective and tailored treatment options for cancer patients. The integration of AI in predicting patient-specific neoepitopes showcases the potential of technology in revolutionizing cancer treatment approaches.
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