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.
羅德島州普羅vidence,2024年12月6日 /PRNewswire/ -- EpiVax,Inc. 是生物製藥和肽類治療的臨床前免疫原性風險評估領域的領先者,慶祝2024年富有成效的一年,標誌着科學創新、服務多樣化和公司增長。
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 擴展了其免疫原性風險評估服務的廣度,推出了ISPRI中的許多新功能(I免疫原性 S篩選和 P蛋白質 R電子工程 Interface) 工具包和許多新評估產品。
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發佈了ISPRI Downselect, Quantify, Analyze, Evaluate, Complete, Optimize和Design按服務收費分析——這些選項評估不同階段的生物製劑,在臨床前開發過程中,能夠對個體候選者進行排名、針對特定方式進行基準測試、序列優化和深入風險分析,提高準確性,等等。今年,對選定的基因治療和CAR-t客戶的ISPRI工具包還增加了I類分析。
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推進了其PANDA篩查程序,以支持進入FDA的簡化新藥申請(ANDA)途徑的贊助商,針對生物肽及其雜質。關鍵更新包括髮布增強型自適應體外檢測產品,以及 先天免疫反應檢測,使EpiVax成爲生物藥開發者的「一個站式商店」(包括計算機模擬、體外和先天評估)。此外,EpiVax和 FDA啓動了一項新合同 開發針對t細胞測試的標準化控制,這將有助於提高該測試的特異性和靈敏性,覆蓋整個行業。
This work was accompanied by notable contributions to the field with the publication of several highly cited articles by the EpiVax team in 2024.
這項工作伴隨着EpiVax團隊在2024年發表的幾篇高引用文章,爲該領域做出了顯著貢獻。
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.
由於擴展了服務,EpiVax的免疫原性風險評估預訂在2023年幾乎激增了60%,這得益於ISPRI訪問、ISPRI收費服務和PANDA服務垂直領域新客戶數量的翻倍。這一成功支持了18%的員工擴張,包括戰略領導的新增,以繼續推動公司的新服務。
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"無畏科學"的指導下,EpiVax準備在今年的成就基礎上,進一步整合人工智能和機器學習的增強功能,以擴展現有平台、實驗室能力,並增加將在新年晚些時候宣佈的科學專業知識。
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.
關於EpiVax
EpiVax是臨床前免疫原性評估和肽治療藥物、生物治療藥物及生物-疫苗序列優化的領導者。EpiVax與全球一系列公司、機構和學術界合作,加速免疫原性風險評估、免疫調節和快速的生物-疫苗設計。
Press Contact
Sarah Moniz
Director, Business Development
EpiVax
[email protected]
新聞媒體聯繫人:
Sarah Moniz
業務發展董事
EpiVax
[email protected]
SOURCE EpiVax, Inc.
來源 EpiVax, Inc.