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XenTech

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.

Features of XenTech's non-clinical contract testing services

Evaluate candidate compounds using patient-derived PDX models

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.

Evaluate not only drug efficacy but also PK/PD, pathology, and biomarkers

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.

Flexible support from standard models to custom models

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.

参照元:XenTech公式サイト
http://www.xentech.eu/

An example of disease models owned by XenTech

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.

参照元:XenTech公式サイト PDX Models
https://www.xentech.eu/models/human-pdx/

XenTech non-clinical study cases

Comparative evaluation of candidate drugs using 21 colorectal cancer PDX models

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.

参照元:XenTech公式資料 A new and fast in vitro screen to predict in vivo drug efficacy using primary cultures from tumorgraft models
https://www.xentech.eu/wp-content/uploads/2021/07/60.pdf

XenTech Corporate Information

参照元:XenTech公式サイト
http://www.xentech.eu/
Address1-7 Imp. Alexis Trinquet, 91000 Évry-Courcouronnes, France
Tel+33 (0)1-608-789-80
Websitehttp://www.xentech.eu/
3 Recommended Contract Research Organizations for Non-Clinical Studies
— by Target goal and Expertise

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.

Pharmacology (Efficacy) Studies
Replicate unknown pathological models and
Discovery to clinically oriented drug evaluation
SMC Laboratories, Inc.
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories, Inc. has established a disease models using patented mouse technologies. The company has established proprietary pathological models—particularly in liver disease and fibrosis—and continues to expand their approach across a wide range of models in cancer, inflammation, and metabolic diseases.
  • From exploratory research to clinically oriented efficacy evaluation, SMC offers customized study designs, dosing strategies, and evaluation analysis tailored to each project. Their collaborative approachallows researchers to discuss and refine study plans together with SMC’s expert scientists.

  • With flexible small-scale study options and strong technical support, SMC Laboratories, Inc. is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
Labcorp Holdings Inc.
(Labcorp Drug Development)
Labcorp Holdings Inc.
Reference: Labcorp Holdings Inc. official website (https://jp.labcorp.com/)
  • Labcorp Holdings Inc. provides a fully integrated GLP testing system aligned with international regulatory standards, including FDA, EMA, and PMDA requirements. All studies are conducted under ICH-compliant quality assurance, making it ready for data submission.
  • The company has extensive expertise in long-term toxicity studies such as Segment I–III reproductive and carcinogenicity studies, as well as 2-year chronic toxicity assessments.
  • Labcorp Holdings Inc.’s comprehensive approach enables sponsors to efficiently outsource the entire preclinical package from toxicology, toxicokinetic (TK), and safety pharmacology study design to execution. This accelerates a path to First-in-Human (FIH) trials. For most of the global drug developers, this all-in-one service structure minimizes cost, risk, and expedite the time before advancing to clinical phase.
Pharmacokinetic (PK/PD) Studies
High-Precision Bioanalysis for Clinically Predictive PK/PD Evaluation
PhoenixBio Co., Ltd.
PhoenixBio Co., Ltd.
Source: PhoenixBio Co., Ltd. Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio Co., Ltd.offers pharmacokinetic and hepatic metabolism studies using their proprietary PXB-mouse®, a humanized-liver chimeric mouse model. This platform enables the acquisition of data with high clinical correlation in ADME, drug–to-drug interaction studies, bridging the gap between preclinical and clinical stages.
  • With advanced LC-MS/MS-based bioanalysis, PhoenixBio Co., Ltd. provides aseamless workflow from plasma concentration measurement and metabolite identification to quantitative validation.

  • The company offersan integrated evaluation analysiscovering pharmacokinetics, hepatotoxicity, and safety with flexibility to accommodate complex modalities such as oligonucleotide and middle-molecule therapeutics. For compounds where hepatic metabolism is a development bottleneck—or where quantitative, reproducible exposure data are critical—PhoenixBio Co., Ltd. delivers unmatched analytical precision and consistency.

By region
list of animal models
Expertise & Track Record
3 Recommended Contract Non-Clinical Testing Services