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Evotec SE

Evotec SE is a global contract research organization (CRO) headquartered in Hamburg, Germany, supporting a broad range of research activities from drug discovery through preclinical development. The company provides in-house nonclinical studies and has established comprehensive testing platforms covering pharmacokinetics, safety evaluation, and translational research.
This page provides an overview of Evotec SE’s nonclinical research capabilities and representative disease models.

Features of Evotec SE’s Contract Services for Non-Clinical Studies

Pharmacokinetic and DMPK studies for comprehensive candidate profiling

Evotec SE conducts integrated evaluation of absorption, distribution, metabolism, and excretion to support the selection of candidate compounds for clinical advancement.
Both in vitro and in vivo DMPK studies are available, including metabolite identification and assessment of drug–drug interactions (DDI).
Advanced analyses such as radiolabeled studies and bioanalysis enable clarification of the relationship between efficacy and safety.
Consistent data generation from hit identification through early clinical stages supports robust development strategy planning.

Safety assessment from discovery-stage screening to GLP-compliant studies

Evotec SE offers end-to-end safety evaluation, from exploratory studies through GLP-compliant repeated-dose toxicity studies, enabling comprehensive toxicity profiling of candidate compounds.
Testing capabilities include general toxicity, genotoxicity, and safety pharmacology, with support for multiple routes of administration such as oral, injectable, and continuous dosing.
In addition, integration with the INDiGO program streamlines generation of nonclinical safety data required for IND submissions, helping to meet regulatory requirements while reducing early development risk.

Integrated development support with a focus on IND submission

With a view toward IND submission and early clinical development, Evotec SE provides integrated support across development, manufacturing, and regulatory functions. More than 4,000 scientific experts support project design across analytical method development, CMC, bioanalysis, and pharmacometrics.
Through the INDiGO integrated IND-enabling package, Evotec SE accelerates transition to first-in-human (FIH) studies while maintaining a development framework scalable through Phase II and III supply.

Examples of Disease Models Available at Evotec SE

Humanized immune system mouse IBD model (DSS-induced)

Colitis is induced in humanized immune system mice using DSS, enabling evaluation of the efficacy of human-specific antibodies and other therapeutic modalities. Dose-dependent inflammatory markers and histopathological changes can be assessed, with inclusion of human cytokine measurements to enhance clinical translatability.

Accelerated diabetic kidney disease model (Renin-AAV db/db Unx)

This model combines renin overexpression, unilateral nephrectomy, and a db/db genetic background to induce hyperglycemia and hypertension. Disease progression, including proteinuria and glomerulosclerosis, can be longitudinally evaluated in a pathological context closely resembling human type 2 diabetes. Benchmarking against standard-of-care therapies is also supported.

Evotec SE Non-Clinical Case Study

Efficacy evaluation in an accelerated diabetic kidney disease model (Renin-AAV db/db Unx)

Using the Renin-AAV db/db Unx model, disease progression driven by hyperglycemia and hypertension was quantified through assessment of proteinuria and glomerulosclerosis.
Benchmarking with standard-of-care treatments enables evaluation of candidate compound efficacy using clinically relevant endpoints such as uACR and glomerulosclerosis scoring.
The study design emphasizes translational relevance to human type 2 diabetic kidney disease.

Evotec case study images
Reference: Evotec SE's official website (https://www.evotec.com/solutions/therapeutic-areas/renal-diseases/in-vivo-renal-disease)
Evotec case study images
Reference: Evotec SE's official website (https://www.evotec.com/solutions/therapeutic-areas/renal-diseases/in-vivo-renal-disease)

Evotec SE Company Information

Address Essener Bogen 7, 22419 Hamburg, Germany
Tel +49 (0)40 560 81-0
Website https://www.evotec.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, 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