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Whole Body Target Expression –XpressWay™ Profiles

Understanding how a therapeutic candidate may impact different systems throughout the human body can help to make more informed development decisions
Using a set of 72 non-diseased human tissues and a validated quantitative reverse transcription-polymerase chain reaction (qRT-PCR) methodology to profile gene expression, Precision has developed XpressWay™ Profiles, a robust, quantitative platform to provide insight into whole body target expression.

XpressWay™ Profiles for target expression

Precision's established XpressWay Profile database contains profiles for more than 2,300 genes, which enables immediate access to robust data for your target(s) of interest. In addition, we can rapidly generate these data profiles for new targets and/or variants on demand.


  • Target validation
  • Safety liability
  • Drug repurposing
  • Validation of animal models
  • 2,300 existing gene profiles available



  • qRT-PCR based for sensitive and quantitative expression data
  • Validated and robust methodology
  • Existing profiles can be leveraged for rapid data delivery, or new profiles can be generated
XpressWay Profiles Example (1)

XpressWay™ Profiles deliver data on how therapeutics may impact tissue and organ systems

Data are generated using 72 non-diseased tissues representing all core organ systems, each tissue from n=3 independent donors. 

This helps provide both a broad and deep understanding of potential physiological impact of a candidate therapeutic.

Scientific in lab

Choose a contract research organization with Precision

A contract research organization (CRO) is crucial to medical research and development to provide support that includes clinical trial management and CRO research. The right outsourced CRO services can accelerate the overall process of drug development and market placement. Whether you need a CRO for clinical trials or a CRO for pharma, Precision has a solution that can be tailored to the needs of your study.

What sets Precision apart from other contract research organizations, is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences. This is Precision Convergence: maximizing insights into patient biology and accelerating the pace of scientific discovery and approval.

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