EpiVax Drives Immunogenicity Innovation in 2024: Year in Review
EpiVax Drives Immunogenicity Innovation in 2024: Year in Review
PROVIDENCE, R.I., Dec. 6, 2024 /PRNewswire/ -- EpiVax, Inc., a leader in preclinical immunogenicity risk assessment for biologic and peptide therapeutics, celebrates a productive 2024 marked by scientific innovation, service diversification, and corporate growth.
罗德岛州普罗vidence,2024年12月6日 /PRNewswire/ -- EpiVax,Inc. 是生物制药和肽类治疗的临床前免疫原性风险评估领域的领先者,庆祝2024年富有成效的一年,标志着科学创新、服务多样化和公司增长。
This year, EpiVax expanded the breadth of its immunogenicity risk assessment services with the launch of many new capabilities in the ISPRI (Immunogenicity Screening and Protein Re-engineering Interface) Toolkit and many new assessment offerings.
今年,EpiVax 扩展了其免疫原性风险评估服务的广度,推出了ISPRI中的许多新功能(I免疫原性 S筛选和 P蛋白质 R电子工程 Interface) 工具包和许多新评估产品。
Notably, EpiVax released the ISPRI Downselect, Quantify, Analyze, Evaluate, Complete, Optimize, and Design fee-for-service analyses – options that assess biologic modalities at different stages of preclinical development, enabling the ranking of individual candidates, modality-specific benchmarking, sequence optimization and in-depth risk analyses with enhanced accuracy, and more. Class I analysis was also added to the ISPRI toolkit this year for selected gene therapy and CAR-T clients.
值得注意的是,EpiVax发布了ISPRI Downselect, Quantify, Analyze, Evaluate, Complete, Optimize和Design按服务收费分析——这些选项评估不同阶段的生物制剂,在临床前开发过程中,能够对个体候选者进行排名、针对特定方式进行基准测试、序列优化和深入风险分析,提高准确性,等等。今年,对选定的基因治疗和CAR-t客户的ISPRI工具包还增加了I类分析。
Further, EpiVax advanced its PANDA Screening program to support sponsors entering the FDA's Abbreviated New Drug Application (ANDA) pathway for generic peptides and their impurities. Key updates included the release of enhanced adaptive in vitro assay offerings and the Innate Immune Response Assay, establishing EpiVax as a "one stop shop" (featuring in silico, in vitro and innate assessment) for generic drug developers. Additionally, EpiVax and FDA-initiated a new contract to develop standardized controls for T cell assays which will help to improve the specificity and sensitivity of such assays industry-wide.
此外,EpiVax推进了其PANDA筛查程序,以支持进入FDA的简化新药申请(ANDA)途径的赞助商,针对生物肽及其杂质。关键更新包括发布增强型自适应体外检测产品,以及 先天免疫反应检测,使EpiVax成为生物药开发者的“一个站式商店”(包括计算机模拟、体外和先天评估)。此外,EpiVax和 FDA启动了一项新合同 开发针对t细胞测试的标准化控制,这将有助于提高该测试的特异性和灵敏性,覆盖整个行业。
This work was accompanied by notable contributions to the field with the publication of several highly cited articles by the EpiVax team in 2024.
这项工作伴随着EpiVax团队在2024年发表的几篇高引用文章,为该领域做出了显著贡献。
As a result of the expanded offerings, EpiVax immunogenicity risk assessment bookings surged nearly 60% over 2023, driven by a doubling of new clientele across the ISPRI Access, ISPRI Fee-for-Service, and PANDA service verticals. This success supported an 18% headcount expansion, including strategic leadership additions to continue driving the company's new offerings.
由于扩展了服务,EpiVax的免疫原性风险评估预订在2023年几乎激增了60%,这得益于ISPRI访问、ISPRI收费服务和PANDA服务垂直领域新客户数量的翻倍。这一成功支持了18%的员工扩张,包括战略领导的新增,以继续推动公司的新服务。
Looking to 2025, guided by nearly three decades of "fearless science", EpiVax is prepared to build on this year's achievements by further integrating artificial intelligence and machine learning enhancements to existing platforms, expanding laboratory capability, and adding scientific expertise that will be announced later in the new year.
展望2025年,在近三十年的"无畏科学"的指导下,EpiVax准备在今年的成就基础上,进一步整合人工智能和机器学习的增强功能,以扩展现有平台、实验室能力,并增加将在新年晚些时候宣布的科学专业知识。
About EpiVax
EpiVax is a leader in preclinical immunogenicity assessment and sequence optimization for peptide therapeutics, biologic therapeutics, and vaccines. EpiVax partners with a global roster of companies, agencies, and academics to accelerate immunogenicity risk assessment, immune modulation and rapid vaccine design.
关于EpiVax
EpiVax是临床前免疫原性评估和肽治疗药物、生物治疗药物及生物-疫苗序列优化的领导者。EpiVax与全球一系列公司、机构和学术界合作,加速免疫原性风险评估、免疫调节和快速的生物-疫苗设计。
Press Contact
Sarah Moniz
Director, Business Development
EpiVax
[email protected]
新闻媒体联系人:
Sarah Moniz
业务发展董事
EpiVax
[email protected]
SOURCE EpiVax, Inc.
来源 EpiVax, Inc.