XenTech isFrench non-clinical CRO specializing in oncology. We have particular strengths in PDX models using patient-derived tumor tissues, and we provide contract services at our own facilities for in vivo efficacy evaluation, PK/PD, and biomarker discovery, among others.
XenTech isPDX model in which patient-derived tumor tissue is transplanted into immunodeficient miceWe are building a drug discovery platform centered on , capable of evaluating drug efficacy using a diverse range of tumor models, focusing mainly on solid tumors such as breast, colorectal, and lung cancer. Because models can be selected taking into account reactivity to standard treatments and molecular characteristics, the effects of candidate compounds can be examined in an environment closer to the clinical setting. Backed by a research foundation with Institut Curie—which has been involved in PDX research since 1989—we have a track record of over 2,500 in vivo studies.
It is possible to combine in vivo efficacy studies with multiple analytical technologies.This is also a feature. In efficacy evaluations, blood analysis, IHC, molecular profiling, etc., can be added, and blood and tissue sampling for PK/PD is also supported. In addition, by comparing PDX drug responses with molecular information such as genetic mutations, copy numbers, and gene/protein expression, biomarkers related to treatment response and resistance can be explored. We support translational research, ranging from confirming the efficacy of candidate compounds to investigating the target patient population.
At XenTech,Configure PDX models and study designs to fit research objectives.It is possible. We provide models that replicate metastasis, models to evaluate residual tumor cells after chemotherapy, and PDXs with acquired resistance to specific treatments. In addition, we support orthotopic transplantation models, bioluminescent PDXs, syngeneic models, and humanized models. The facility is an ISO 9001-certified vivarium, and we also undertake custom studies tailored to your research objectives. Please note that since GLP certification cannot be confirmed on the official website, prior confirmation is necessary if GLP-compliant studies are required.
At XenTech,PDX models derived from treatment-resistant cancer patientsWe are deploying the MATCH-R collection, which includes [insert term], models generated from tumors of patients who experienced disease progression after an initial response to treatment. These can be used to analyze mechanisms of acquired resistance and explore new therapeutic approaches. For breast cancer, it covers multiple subtypes such as triple-negative.
XenTech isPreclinical phase II-like trial using 21 colorectal cancer PDX modelsWe are publishing research results evaluating multiple standard therapies as single agents or in combination, comparing drug reactivity across tumor models. By reproducing the biological diversity of tumors found in patient populations using PDX panels, this is utilized in research examining the efficacy of candidate drugs and the selection of appropriate models.
| Address | 1-7 Imp. Alexis Trinquet, 91000 Évry-Courcouronnes, France |
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| Tel | +33 (0)1-608-789-80 |
| Website | http://www.xentech.eu/ |
In drug discovery, the quality and efficiency of non-clinical studies have a direct impact on clinical success rates, development costs, and overall length of time required in R&D.
In recent years, there has been more demand for clinically relevant data, globally accepted reliability, and accurate early-stage screening.
Thus, it is more important than ever to select the right CRO (Contract Research Organization) for strategic approach.
In this article, we highlight three CROs with proven technical capabilities, expertise, and long standing track records. These are our TOP 3 choices based on their capabilities and the specific target goals of the researchers for their non-clinical studies.