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Gubra

Table of Contents
Table of Contents

Based in Denmark, Gubra is a non-clinical CRO with strengths in metabolic diseases and fibrosis. It provides rapid and reliable drug discovery support by utilizing its proprietary pathological models and advanced analytical technologies. Here, we introduce in detail the features of Gubra's services and specific study cases.

Features of Gubra's Contract Non-clinical Trial Services

Specialization and reliability in the area of metabolism and fibrosis

Gubra is deeply specialized in the metabolic and fibrosis areas of obesity, diabetes, and MASH (metabolic insufficiency related steatohepatitis). The company's major strength is that it is an "R&D-oriented" company with its own drug discovery pipeline, not merely a contract research company.

Our scientific proposals are very practical, based on abundant research data and experience gained from our actual in-house drug discovery activities. We believe that we can be your reliable partner to lead your drug discovery project to success.

Advanced technology using AI analysis and 3D imaging

Another major advantage of selecting Gubra is its proactive implementation of advanced technologies to improve data quality. In particular, 3D imaging technology, which makes entire organs transparent for imaging, and AI-based histological analysis provide extremely accurate data.

It visualizes microscopic lesions and drug distribution that cannot be captured by conventional analysis methods and can be used as objective evidence. It is a powerful weapon for researchers who want to make more reliable decisions.

An example of Gubra's pathological model

MASH (steatohepatitis) model that faithfully reproduces human pathology

Gubra's GAN DIO-MASH mouse model faithfully reflects human pathophysiology. It is highly valued for its ability to confirm progression by liver biopsy and provide highly predictive clinical data.

This is a strong option for those looking for a highly accurate test system.

Obesity and diabetes models with extensive experience

The high-fat diet-induced obesity (DIO) model, with over 15 years of experience, is another of Gubra's major strengths. In addition to food intake and energy metabolism, Gubra supports a wide range of assessments, including brain activation signatures.

The model, filled with our unique know-how, will greatly contribute to the elucidation of the mechanism of action.

Gubra Non-clinical Case Studies

Imaging case study to visualize drug action in the brain in 3D

Gubra's "Whole Brain 3D Imaging" is a revolutionary technology that visualizes which parts of the brain are activated by a drug. For example, in the evaluation of anti-obesity drugs, Gubra has successfully mapped the expression of "c-Fos," an indicator of neural activity, at the single cell level to identify the mechanism of action (MoA) of the drug.

A major advantage of this method is that the entire brain is analyzed without slicing, so the entire picture can be obtained without omission. This can be used as a convincing scientific basis for the development of drugs that act on the central nervous system.

Application of AI Pathology Analysis in Renal Disease Models

Image analysis using artificial intelligence (AI) has been successful in tests to evaluate fibrosis in kidneys. Using AI, the quantification of fibrosis areas, which tends to vary with conventional visual evaluation by pathologists, can be done quickly and objectively.

There have been cases where the effect of microscopic treatment was accurately detected in models of chronic kidney disease (CKD) and diabetic kidney disease (DKD). This is a reliable analysis method for researchers who value data reproducibility.

Gubra Company Information

Headquartered in Denmark, Gubra is a highly specialized biotechnology company focused on the metabolic and fibrosis areas. The company accelerates drug development worldwide through both advanced contract non-clinical research services (CRO) and in-house peptide drug discovery research.

Address Hørsholm Kongevej 11B, 2970 Hørsholm, Denmark
Tel +45 3152 2650
Website https://www.gubra.dk/
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