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FibroFind

Table of Contents
Table of Contents

FibroFind is a Newcastle, UK-based contract non-clinical testing organization specializing in fibrotic diseases. Combining years of research experience with proprietary technologies, FibroFind provides strong support for drug discovery and development.

This article will provide a detailed explanation of the company's service features and disease models.

Features of FibroFind's preclinical contract services

Proprietary human tissue slicing technology (PCTS)

One of FibroFind's key features is its Precision Cut Tissue Slices (PCTS) technology using human tissues. Unlike traditional cell cultures, it allows for drug evaluation while maintaining the complex environment found in living organisms.

This allows for more accurate prediction of human response prior to transfer to clinical trials. I believe that this technology will make a significant contribution to reducing development risks.

Extensive track record in fibrotic disease research

Our strengths include specialization in fibrotic diseases of the liver, kidneys, and lungs, backed by decades of research experience. Our team of experts, equipped with extensive knowledge, proposes study designs tailored to client needs.

Rather than simply acting as a contractor, we function as a partner in the drug discovery process. We have established a system that can strongly support research and development through the provision of reliable data.

An example of FibroFind's pathological model

Human liver PCTS (precision-cut liver sections)

This is a highly accurate slice model that retains the main structure and cellular environment of human liver tissue. It allows for evaluation of cell-cell interactions and the matrix environment, which are difficult to reproduce with conventional cell cultures, enabling data acquisition that reflects clinical-like responses in efficacy studies of novel drugs for liver fibrosis (such as NAFLD/NASH).

Kidney and lung fibrosis models

Human kidney and lung disease models that apply proven PCLS technology from the liver. They reproduce the fibrotic mechanisms in idiopathic pulmonary fibrosis (IPF) and chronic kidney disease (CKD), and are used to evaluate tissue responses to inflammation-inducing stimuli and the antifibrotic effects of standard therapeutic drugs.

Reference: FibroFind Official Website
https://www.fibrofind.com/human-fibrotic-diseases/

FibroFind Non-clinical Case Studies

Drug Efficacy Evaluation Study of a Novel Antifibrotic Drug

This is a study to measure the anti-fibrotic effect of a compound under development by administering it to a human liver PCTS model. Comparisons with standard of care (SOC) drugs and confirmation of dose-dependency will be performed.

Because actual human tissues are used, we have a great deal of experience in obtaining predictive data that complement mouse models and are useful as a bridge to clinical practice.

Mechanism of action (MoA) elucidation and target exploration study

This is a test that analyzes the variations of specific genes and proteins using models of the kidneys and lungs. By combining techniques such as transcriptome analysis (RNA-seq), it is possible to precisely identify the pathways by which a drug inhibits fibrosis. This is utilized as a case in validating drug discovery targets.

Reference: FibroFind Official Website
https://www.fibrofind.com/publications/

FibroFind Company Information

FibroFind is a biotechnology company originating from Newcastle University in the UK. In 2025, with investment from Vespa Capital, it continues to grow as a global contract research organization combining many years of research achievements with a strong management foundation.

Our strength is that we combine the precision of a university laboratory level with the speed that industry demands. With pharmaceutical and biotech companies around the world as our clients, we operate globally.

Address Unit 26-27, The Pantry Bakers Yard, Christon Road, Newcastle Upon Tyne, NE3 1XD, UK
Tel Not open to the public (please use the contact form on the official website)
Website https://www.fibrofind.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 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