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Explicyte

Explicyte is a CRO that provides preclinical testing services specializing in the field of cancer immunotherapy. Utilizing highly accurate cell assays, animal models, and advanced spatial biology analysis,Supports R&D for pharmaceutical and biotech companies worldwideThis article provides a detailed introduction to Explicyte's features, its available disease models, and examples of non-clinical studies. Please use this as a reference when choosing a contract research organization.

Characteristics of Explicyte's Non-clinical Testing Contract Services

Compatible with a wide range of cell-based immune assessment assays

Explicyte conducts a wide range of in vitro (cell-level) tests specifically for cancer immunotherapy. Typical examples include:Immune checkpoint inhibitor assays (PD-1/PD-L1, CTLA-4, etc.), antibody-dependent cell-mediated cytotoxicity (ADCC), tumoricidal assays, and the like. These tests allow for precise evaluation of the interaction between immune cells and tumor cells, as well as therapeutic effects. Furthermore, we can also support mixed lymphocyte reactions (MLR), macrophage function assays, and cytokine release assays. The flexibility to customize based on research themes and development stages is a major strength of Explicyte's in vitro assays.

One-stop support from test design to data analysis

Explicyte, not only for cell testing,We have established a system to complete in vivo (animal model) studies and human sample analysis in-house. In particular, the evaluation of immune responses using syngeneic tumor models is highly valued for its ability to reproducibly verify the effects of anticancer drugs and immune checkpoint inhibitors. We also focus on translational research with a view to clinical application, providing comprehensive research support by combining the latest technologies such as biomarker discovery and spatial biology analysis. As a "CRO that can handle everything from study design to analysis," we have earned the trust of bio-companies worldwide.

An example of a disease model held by Explicyte

When selecting a contract research organization (CRO), the variety and reliability of their disease models are important decision-making factors. Explicyte specializes in cancer immunotherapy research and offers a diverse range of models, including syngeneic tumor models where the immune system functions. Here, we will present examples of representative models and outline their characteristics and use cases.

Immunological response evaluation model using mice (syngeneic tumor model)

One of Explicyte's representative models is the syngeneic tumor model in mice, which can be evaluated with a functioning immune system. In this model, syngeneic tumor cells are transplanted into inbred mice, allowing observation of the interaction between tumors and immune cells under physiologically relevant conditions. For immune checkpoint inhibitors, CAR-T, NK cell therapies, etc.,It is suitable for verifying the effectiveness of therapies that utilize the immune system. In Explicyte, it is used for evaluating major immunotherapies such as anti-CTLA-4 antibodies and anti-PD-1/PD-L1 antibodies, and changes in the immune microenvironment can be understood through multiplex immunohistochemistry and spatial analysis.

Biomarker Discovery Model Using Human Samples (Translational Research)

Explicyte focuses on translational research using not only animal models but also human-derived samples. By analyzing clinical samples such as tumor tissue and blood, they support the discovery of new cancer treatment targets and biomarkers. This enables them to assist in the design and hypothesis testing of translational research, bridging the gap from preclinical stages to clinical trials. They can visualize patient-specific immune responses and treatment efficacy variations that are difficult to discern with animal studies alone.It is useful as a practical validation model for the development of cancer immunotherapy.

Explicyte's Non-clinical Trial Cases

Immune checkpoint inhibitor efficacy verification trial

Explicyte is conducting preclinical studies of immune checkpoint inhibitors using syngeneic tumor mouse models. A representative example is the evaluation of the efficacy of anti-PD-1 and anti-PD-L1 antibody therapies using a colorectal cancer model (MC38). In addition to the tumor growth inhibitory effect,We are investigating the mechanisms of treatment response by analyzing immune cell infiltration and cytokine dynamics.

Translational research for biomarker discovery

At Explicyte, we are also advancing the exploration of novel biomarkers through translational research using clinical samples. We analyze tumor tissues and blood samples to support prediction of immunotherapy efficacy and identification of therapeutic targets. By combining spatial biology and single-cell analysis technologies,You can accurately grasp the immune cell dynamics within the tumor microenvironment (TME). These analysis results are utilized as important findings to improve the precision of clinical applications and treatment strategies.

Explicyte Company Information

Explicyte is a preclinical and translational research CRO specializing in the development of cancer immunotherapies. Based in Bordeaux, France, we support the research and development efforts of pharmaceutical companies and bioventures not only in Europe but also globally, including North America, Japan, and South Korea.

Address 229 Cours de l'Argonne, 33000 Bordeaux, France
Tel +33 (0)5 64 31 11 70
Website https://explicyte.com/
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 official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories 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 is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
labcorp
(Labcorp Drug Development)
labcorp
Reference: labcorp official website (https://jp.labcorp.com/)
  • labcorp 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’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
PhoenixBio
Source: PhoenixBio Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio 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 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 delivers unmatched analytical precision and consistency.

Consult Phoenix Bio for PK/PD analysis with a clinical focus