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.
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.
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.
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.
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.
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.
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.


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