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 |
|---|---|
| Tel | +33 (0)1-608-789-80 |
| Website | http://www.xentech.eu/ |
In non-clinical development, the choice of contract research organization shapes the quality of the data and the time it takes to reach the next decision. Below, three CROs are introduced by the type of study they support: pharmacology (efficacy) studies, safety studies, and pharmacokinetic (PK/PD) studies. Each summary describes the services the company offers so that you can match a provider to your target and development objective.
SMC Laboratories is a specialized non-clinical CRO focused on in vivo pharmacology and efficacy studies using disease-relevant animal models, particularly in fibrosis, inflammation, metabolic diseases, and oncology.
SMC Laboratories offers models covering the liver, lung, kidney, intestine, and oncology. Its portfolio includes the proprietary STAM™ model for MASH, fibrosis, and hepatocellular carcinoma.
Study plans are developed around the target biology, mechanism of action, disease stage, and development objective. Pharmacological endpoints can be combined with histopathology, biomarkers, and disease-specific readouts.
With experience from more than 1,000 studies for clients in 30 countries, SMC Laboratories supports programs from target validation and candidate selection through in vivo proof-of-concept studies.
Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.
Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.
Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.
Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.
Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.
PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.
Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.
Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.