Nonclinical Efficacy Testing » Non-Clinical CROs and Agencies » Physiogenex SAS

Physiogenex SAS

Physiogenex SAS is a nonclinical contract research organization (CRO) based in Toulouse, France,specializing in metabolic diseases, including obesity, type 2 diabetes, NASH/MASH fibrosis, diabetic nephropathy, inflammation, dyslipidemia, and cardiovascular diseases.
Founded in 2003, the company has more than 20 years of experience providing pharmaceutical and biotechnology companies with services such as drug efficacy evaluation and mechanism-of-action analysis.

Features of Physiogenex SAS’s Contract Services for Non-Clinical Studies

Deep expertise in metabolic diseases

The company offersmetabolic disorders such as NASH, diabetes, and obesity,and has developed highly predictive in-house animal models, including hamster and rat models. These models enable efficacy studies under conditions with strong clinical relevance.
Leveraging extensive experience in the field, the company delivers not only robust datasets but also interpretative reports that provide insights into disease mechanisms and translational relevance.

proprietary CRO consulting to support clients’ drug development strategies.

In addition to experimental services, Physiogenex SAS offersproprietary CRO consulting to support clients’ drug development strategies.These services are designed to reduce development timelines and costs while facilitating successful progression toward market entry. Consulting activities include comprehensive literature reviews and in-depth analysis of compound- and target-related data. Continuous interaction with clients is maintained through regular teleconferences and on-site meetings.

Commitment to GLP-based quality standards

Physiogenex SAS’s quality system isbased on Good Laboratory Practice (GLP) principles.By adhering to established operational policies, the company ensures data consistency, traceability, and reliability. In addition,Physiogenex SAS has implemented a quality management system compliant with ISO 9001:2015 requirements,further reinforcing its commitment to high-quality research standards.

Examples of Disease Models Available at Physiogenex SAS

Physiogenex SAS maintainsa broad portfolio of animal models,The company is doing so.

For example, type 1 diabetic rat models induced by streptozotocin (STZ) are used to evaluate blood glucose control, postprandial glucose responses, and mechanisms of action of test compounds. The company also offers acute liver failure models designed to assess liver regeneration, survival improvement, and biomarker responses, supporting comprehensive evaluation of therapeutic candidates.

Physiogenex SAS Non-Clinical Case Study

Evaluation of postprandial glucose-lowering effects of a specific collagen hydrolysate

Physiogenex SAS evaluated the ability of a specific collagen hydrolysate to suppress postprandial blood glucose elevation. In mouse studies, oral administration significantly improved glucose tolerance in both healthy mice and obese, pre-diabetic models.

In a human clinical study involving 16 healthy adults and individuals with prediabetes, ingestion of 5 g or 10 g of the collagen hydrolysate 30 minutes before meals resulted in an average reduction of postprandial glucose spikes by 40–43%.

These findings suggest thatthe specific collagen hydrolysate may support endogenous GLP-1 activityand contribute to the maintenance of metabolic health.

Referred to WILEY Online Library (https://onlinelibrary.wiley.com/doi/10.1002/fsn3.4538)

Physiogenex SAS Company Information

Founded in 2003, Physiogenex SAS provides preclinical CRO services and consulting focused on metabolic diseases. In addition to standard CRO activities, the company acts as a research and development partner, offering customized evaluation models and study designs tailored to client needs.
Physiogenex SAS also provides in vivo preclinical imaging services.

Address280 rue de l'Hers, ZAC de la Masquère, 31750 Escalquens, France
Tel+33 (5)32-097-980
Websitehttps://www.physiogenex.com

3 Recommended Contract Research Organizations
for Non-Clinical Studies
— by Target goal and Expertise

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.

Pharmacology (Efficacy) StudiesDisease-Relevant Models for
Translational Drug Evaluation
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/)

SMC Laboratories, Inc.

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.

Areas of Expertise
Disease-Relevant Model Portfolio

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 Design Based on Target Biology

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.

Support from Target Validation to Proof of Concept

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.

Safety StudiesComprehensive Safety Assessment for
Preclinical Development
Charles River Laboratories
Reference: Charles River Laboratories official website (https://www.criver.com/)

Charles River Laboratories

Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.

Areas of Expertise
General Toxicology Across Study Designs

Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.

Non-GLP and GLP Study Support

Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.

Integrated IND-Enabling Safety Assessment

Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.

Pharmacokinetic (PK/PD) StudiesConnecting Drug Exposure with
Pharmacological Response
Inotiv
Reference: Inotiv official website (https://www.inotiv.com/)

Inotiv

Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.

Areas of Expertise
Pharmacokinetic Characterization

PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.

Exposure–Response Evaluation

Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.

Integrated DMPK and Development Support

Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.

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