Immusmol SAS 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 Immusmol SAS's features, its available disease models, and examples of non-clinical studies. Please use this as a reference when choosing a contract research organization.
Immusmol SAS 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 Immusmol SAS's in vitro assays.
Immusmol SAS, 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.
When selecting a contract research organization (CRO), the variety and reliability of their disease models are important decision-making factors. Immusmol SAS 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.
One of Immusmol SAS'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 Immusmol SAS, 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.
Immusmol SAS 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.
Immusmol SAS 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.
At Immusmol SAS, 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.
Immusmol SAS 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/ |
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.