# EpiVax Announces Laboratory Expansion and Streamlined, NAM-Centric In Vitro Services

- Link: https://www.thailand-business-news.com/pr-news/epivax-announces-laboratory-expansion-and-streamlined-nam-centric-in-vitro-services
- Published: 2026-06-23T20:12:00+07:00
- Author: PR Newswire

|   |

PROVIDENCE, R.I., June 23, 2026 /PRNewswire/ — EpiVax, Inc., a recognized leader
in immunogenicity risk assessment, announces the expansion of its laboratory facilities
at its Providence, RI headquarters. The upgraded space has more than doubled the
company’s laboratory footprint, expanding the CRO’s capacity to support advanced
immunological testing. This investment reflects growing demand for integrated, human-
relevant, new approach methodologies (NAMs) to evaluate immunogenicity risk due 
to limitations of traditional animal models to provide human-relevant immunogenicity readouts.

Per global regulatory agency guidance, NAMs have become a central component of preclinical
immunogenicity risk assessment for biologics, peptides, emerging modalities, generics/
biosimilars, and critical quality attributes (CQAs). It is suggested that immunogenicity
should not be viewed solely as a late-stage clinical observation, but rather as 
a mechanistically informed, human-relevant risk continuum that can be interrogated
early and throughout development using integrated in silico and in vitro systems
to characterize specific components of immune activation before clinical exposure
and to inform optimized bioanalytical and clinical strategies.

With best-in-class in silico immunogenicity risk assessment tools, a comprehensive
suite of in vitro assays fit to assess innate and adaptive immune responses, a team
of renowned experts, and now an expanded laboratory capacity, EpiVax is well-positioned
as a preferred "one stop shop" partner for a multidimensional, NAM-centric immunogenicity
risk assessment (IRA) for therapeutic developers.

EpiVax’s laboratory supports assessments in human whole blood, PBMC, and specialized
professional antigen presenting cells, such as dendritic cells. The platform assays
are scalable and modular – designed to fit the development phase, therapeutic modality,
throughput, and immunological question at hand – leveraging cellular activation 
through phenotyping, proliferation, and cytokine secretion readouts to evaluate 
the impact of immune liabilities on different aspects of innate and adaptive immune
responses.

The tailored assays provide complementary insights to EpiVax’s in silico analyses(
the ISPRI toolkit), enabling a comprehensive risk assessment consisting of orthogonal
methods, with the benefit of streamlined workflows, data consistency, and inclusive
scientific collaboration.

EpiVax has a strong demonstrated history in the application of its multi-phased 
in silico and in vitro immunogenicity risk assessment approach, including its PANDA
screening framework for generic peptide products. This approach integrates computational
analysis with targeted in vitro methods to assess sequence- and CQA-driven risk 
and establish comparability to reference products. EpiVax has supported more than
16 successful global regulatory submissions in recent years using this framework,
 demonstrating its effectiveness in enabling rigorous, mechanism-based IRAs aligned
with evolving regulatory expectations.

"EpiVax aims to provide human-relevant computational and immune-cell based IRA solutions
that allow therapeutic developers to make more informed, data-driven decisions from
discovery through commercialization," said Vibha Jawa, Ph.D., CSO of EpiVax. "The
expansion of our laboratory will allow us to support our partners in this goal more
efficiently than ever before."

**About** **EpiVax****:EpiVax partners with biologic developers to manage immunogenicity
risk throughout the product lifecycle. Leveraging deep scientific expertise to apply
industry-leading in silico analyses and in vitro approaches, insights from actionable
data help our partners reduce uncertainty, mitigate risk, and use resources more
efficiently while building regulatory-ready strategies for safer, more effective
therapies. [www.epivax.com](https://edge.prnewswire.com/c/link/?t=0&l=en&o=4716883-1&h=4107858614&u=http%3A%2F%2Fwww.epivax.com%2F&a=www.epivax.com)

**Media Contact:Sarah Moniz, Director of Business Development & Marketing
[smoniz@epivax.com](https://www.thailand-business-news.com/pr-news/smoniz@epivax.com)

Logo – [https://mma.prnasia.com/media2/542055/EpiVax_Logo.jpg?p=medium600](https://edge.prnewswire.com/c/link/?t=0&l=en&o=4716883-1&h=230623963&u=https%3A%2F%2Fmma.prnewswire.com%2Fmedia%2F542055%2FEpiVax_Logo.jpg&a=https%3A%2F%2Fmma.prnewswire.com%2Fmedia%2F542055%2FEpiVax_Logo.jpg)

 

---

  |  This article was produced by Cision PR Newswire, our trusted news partner. The views expressed and the content presented here are solely those of the author and may not fully reflect the opinions of Thailand Business News. |

---

 
**Read the original article :** [EpiVax Announces Laboratory Expansion and Streamlined, NAM-Centric In Vitro Services ](http://www.prnasia.com/story/archive/4989272_AE89272_0?rand=184833)
