Nonclinical Efficacy Testing » Non-Clinical CROs and Agencies » FibroFind

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

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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
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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
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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
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Reference: Inotiv official website (https://www.inotiv.com/)

Inotiv

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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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