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Recognized Experts in ADME / DMPK / DDI by 98% of top pharma & countless others for drug metabolism and drug-drug interaction expertise.

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May 1st Transition of XenoTech.com Products and Services to BioIVT.com

Since XenoTech joined BioIVT in Sept. 2022, we have been working to migrate all of the products and services to...

XenoTech Joins BioIVT: Expands Biospecimens Portfolio and Research Services

BioIVT, a leading provider of research models, biospecimens and research services for drug discovery and development has acquired XenoTech Along...

Webinar: New 2022 Draft ICH Drug Interaction Studies Global Guideline

Presenter: Brian Ogilvie, Ph.D, Vice President of Scientific Consulting at XenoTech Drug-drug interactions (DDI) may occur when taking two (or...

Great reports that are ready for submission to the Agency!

Pharma Senior Vice President of R&D

Every XenoTech employee I had contact with throughout these studies have been a pleasure to work with. The entire process was seamless. I never had...

Regulatory Affairs for Small Pharma

There is a lot of quality, skilled work that has gone into this data set. Compared to organizations that have done this type of work...

ADME Consultant

Great reports that are ready for submission to the Agency!

Pharma Senior Vice President of R&D

Every XenoTech employee I had contact with throughout these studies have been a pleasure...

Regulatory Affairs for Small Pharma

There is a lot of quality, skilled work that has gone into this data...

ADME Consultant

Your drug’s journey…

Your drug’s journey…

057 liver and stomach Created with Sketch.

through the body

through the pipeline

Absorption, Distribution, Metabolism, and Excretion (ADME) properties of a xenobiotic describe its disposition and inform overall fate following administration. XenoTech serves 98% of top pharma and countless others by providing high-quality contracted ADME studies and test systems to precede or support clinical trials.

Drug Metabolism & Pharmacokinetics (DMPK) is a core discipline in drug discovery and development investigating how a drug is broken down and cleared, considering both ADME and DDI characteristics to evaluate and optimize properties of a new drug compound. Our drug metabolism and pharmacokinetics testing and products allows sponsors to understand properties of their compounds and to evaluate risk early in drug development and testing.

Drug-Drug Interaction (DDI) studies allow a drug developer to investigate the potential of a xenobiotic compound to interact with drug-metabolizing enzymes and drug transporters to predict the impact on the pharmacokinetics of the compound or coadministered drugs. Drug metabolism and drug transporter studies provide critical information in evaluating potential for drug-drug interactions and associated risks in preclinical drug development.

In Silico Modeling uses mathematical models to evaluate in vitro data in a way that provides meaningful risk prediction for drug metabolism and drug interaction issues later in development or clinical trials.

In Vitro Studies & Test Systems allow drug developers to use cell-based assays to determine ADME/PK characteristics and DDI potential of their drug compound.

Our In Vivo ADME / PK Studies use radiolabeled drug compound administered to laboratory animals to investigate an investigational compound’s pharmacokinetic propertiesinclusing drug metabolism and DDI risk.

FDA
NIH Leadership 2012
We need better drugs. We need to do better. We need to go faster and be more successful
FDA Commissioner 2017
We need to make sure we’re taking steps to foster innovation and regulating areas of promising new technology in ways that don’t raise the cost of drug development or reduce innovation.
XenoTech facilitates the development of safer drugs with fewer failures and lower costs through our state-of-the-art drug metabolism and DDI testing programs to help drug developers understand as much as possible about their drug's metabolism and pharmacokinetics to properly evaluate related drug safety risks.
Over $2.8 billion is spent on the development of each launched drug
Only 1 in 10,000 potential drug compounds make it all the way through the development pipeline
Over 80% of investigational new drugs fail because of unsatisfactory ADME/Tox

Access ADME™ | Scientific Resources