News & Events

Upcoming Conferences

Monday, December 31, 2018

Please note: Sekisui XenoTech attends too many events to be able to list them all here. If you would like to meet with us at a particular event that you do not see listed below, please contact us to schedule a meeting. Thank you!

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Sekisui XenoTech Hiring and Growing to Meet Customer Demand

Wednesday, January 03, 2018

The company hired a record number of new staff over the past year in order to meet current demand for its products and services, which are utilized to optimize the discovery, development, and approval of new drugs and other compounds. Several previous Sekisui XenoTech employees also returned to the company...

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Webinar: Comparison Between the New US FDA and Japan PMDA In Vitro DDI Guidance Documents…

Tuesday, December 19, 2017

After recent revisions to the Japan PMDA 2014 guideline and US FDA 2012 draft guidance for industry on in vitro drug-drug interaction (DDI) studies, Drs. Andrew Parkinson, XPD Consulting, and Brian Ogilvie, Sekisui XenoTech, will offer their expert perspectives on major changes and differences between the two agencies’ in vitro guidance documents, and how to harmonize your drug development strategies to meet the expectations of both...

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Webinar: Essential Considerations on the New FDA In Vitro DDI Guidance

Tuesday, November 21, 2017

In October, the FDA revised and split its 2012 draft guidance for industry on in vitro drug-drug interaction (DDI) studies, into one document for in vitro DDI studies, and another for clinical DDI studies. Dr. Brian Ogilvie offers expert perspective on major changes to the in vitro guidance, whether they will impact your drug development strategy, and with more than two decades of experience in the area what Sekisui XenoTech’s strategy is to address potential development challenges presented by the draft.

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Sekisui XenoTech Appoints New COO

Wednesday, October 18, 2017

Sekisui XenoTech has announced the appointment of Dr. Darren Warren, PhD, as the company’s new Chief Operating Officer. Dr. Warren has over 15 years of leadership experience with Contract Research Organizations (CROs) and almost 30 years of leadership experience in the pharmaceutical industry...

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New Enhanced AO & XO Activity Test Systems Available, Major CYP Activity Not Significantly Impacted

Monday, August 14, 2017

Sekisui XenoTech has established a method for high aldehyde oxidase and xanthine oxidase activity without significantly impacting major CYP activity in pooled human liver S9 and cytosol in vitro drug development test systems…

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Sekisui XenoTech Awarded Cryopreservation Patent, Achieves Numerous Hepatocyte Enhancements

Tuesday, May 09, 2017

Sekisui XenoTech was issued U.S. Patent No. 9,642,355 for the “CRYOPRESERVATION OF CELLS AND SUBCELLULAR FRACTIONS,” specifically related to the CryostaX® test systems, the only single-freeze pooled hepatocytes in the industry, and enhanced its catalog of hepatocyte products with increased cell yield, viability and more...

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Sekisui XenoTech Adds New Dermal Subcellular Fraction Test Systems

Wednesday, February 01, 2017

Sekisui XenoTech is adding human and minipig to the company’s list of species with dermal subcellular fractions available as standard test systems for the development of safer new products. Subcellular fractions are widely used in drug discovery and preclinical drug development to evaluate the in vitro metabolism of new therapeutics.

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Sekisui XenoTech Introduces Lysosomal Test Systems for Biopharmaceutical Development

Wednesday, October 05, 2016

Hepatic human lysosomes and rat tritosomes are now available as standard test systems. These products contain high concentrations of lysosomal degradative enzymes and constitute advantageous test systems for analysis of catabolism and/or activation for targeted biopharmaceuticals that enter cells through the endosomal-lysosomal pathway...

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Sekisui XenoTech Expands Hepatotoxicity Testing Services

Wednesday, August 03, 2016

Adds Assays, Methodologies to Prevent Failure of New Drugs from Liver Injury...

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Sekisui XenoTech Introduces New Research BioBank

Monday, June 13, 2016

As part of Sekisui XenoTech’s commitment to furthering knowledge of hepatic diseases, the company has begun providing disease-diagnosed tissue samples and hepatocytes through its new Research BioBank.

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XenoTech Provides Genotyped Hepatocytes for Polymorphic Enzyme Drug Metabolism Studies

Tuesday, April 12, 2016

Geneknown™ hepatocytes are genotyped cryopreserved human hepatocytes pooled to study the effects of specific genetic variants on drug metabolism and transport to identify risks of adverse drug interactions present only in genetically-defined subpopulations of patients. Genetically determined transport and metabolism polymorphisms have been recognized by the FDA as having potential safety and efficacy implications. This is particularly important for poor metabolizers in cases of drugs metabolized predominantly by polymorphically expressed enzymes.

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XenoTech Accepting Global Scientific Achievement Award Nominations for 2015

Monday, May 18, 2015

XenoTech is accepting nominations for the 2015 Global Scientific Achievement Award, presented annually in recognition of meritorious, scientific contribution and achievement to further research in the field of ADME / DMPK. The recipient will be recognized at an upcoming industry event and will receive an honorarium, travel support, complimentary meeting registration and a $1,000 donation in their name.

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XenoTech Provides Pooled Human Liver Homogenate for Evaluation of Drug Metabolizing Enzymes and Proteins

Tuesday, April 28, 2015

Sekisui XenoTech now offers pooled human liver homogenate. This test system is ideal for metabolism identification when responsible enzymes are not known, proteomic assays, enzymatic activity studies, etc.

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XenoTech Plans Expansion to New Global Headquarters after Impressive Revenue Growth in 2014

Tuesday, April 21, 2015

Contract Research Organization, XenoTech, plans move into new global headquarters and expansion of service offerings after experiencing sizable revenue growth in 2014.

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Case Study: XenoTech Ensures Quality

Monday, April 20, 2015

One company's path to accurate, reliable data in drug discovery: When your lab is one of the last stops before a compound goes into human trials, data quality is vital. Despite increasing throughput and more demanding timelines, one CRO delivers quality - consistently.

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XenoTech Scientists Solve Long-Standing Mystery in Drug Metabolism

Wednesday, January 21, 2015

XenoTech has published a new scientific paper in Drug Metabolism & Disposition that solves the long-standing mystery regarding the lack of in vitro formation in classical test systems and the enzymes responsible for the formation of 3-hydroxydesloratadine, a major active human metabolite of loratadine (Claritin).

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XenoTech Teams Up with JCRB to Provide Access to Over 1,100 Cell Lines in North America

Wednesday, January 07, 2015

XenoTech and the National Institute of Biomedical Innovation have teamed up to bring over 1,100 unique cell lines to the North American market.

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XenoTech Receives US Patent for Its Novel Approach to Evaluate Therapeutic Proteins as Immune Modulators of Drug Metabolism

Tuesday, December 09, 2014

XenoTech has been awarded US patent # 8,846,576 “In Vitro Test System to Evaluate Xenobiotics as Immune-Modulators of Drug Transport and Metabolism in Human Hepatocytes”

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Joint XenoTech / Provectus Article Published by Xenobiotica

Monday, January 27, 2014

XenoTech Aides In Provectus PV-10 Assessment for Drug-Drug Interaction Potential, Published in Xenobiotica

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Tuesday, October 01, 2013

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