SHIN NIPPON BIOMEDICAL LABORATORIES, LTD. (SNBL) is a group of companies that can undertake all stages of nonclinical studies and clinical bioanalysis. This page outlines the features of SNBL’s nonclinical studies, an example of a disease model, and case studies. Use the following information as a reference when selecting a contract research organization (CRO).
Since its establishment in 1957, SNBL has maintained a leading share in Japan in contract nonclinical testing. Leveraging extensive experience in drug development and continued investment in new equipment, SNBL is recognized by pharmaceutical companies as a trusted development partner. In particular, SNBL demonstrates high accuracy in evaluating the efficacy and safety of new drug candidates and provides data in a timely manner.
SNBL breeds and supplies non-human primates (NHPs) within its corporate group. For emerging modalities such as nucleic acid therapeutics and gene therapies, SNBL can reliably supply animal models required for development.
SNBL conducts nonclinical studies using a diverse portfolio of disease models. In particular, SNBL has developed ocular disease models, including glaucoma and age-related macular degeneration (AMD), and has strong capabilities in efficacy/pharmacology studies using these models. The company is also advancing development of an intranasal (IN) drug-delivery system utilizing nose-to-brain technology and is engaged in brain disease model research.
It is essential to go through the testing of candidate compounds in animal models that reproduce the target disease before advancing to clinical trials.
However, clinically relevant disease models may not always exist, thus there are demands for animal models with strong clinical correlation.
Below are some examples of disease models offered at Ina Research.
SNBL conducts nonclinical studies using various disease models. In particular, SNBL has developed monkey models of glaucoma and age-related macular degeneration and conducts contract efficacy/pharmacology studies using these models, supporting pharmaceutical companies in the development of new therapeutics for these diseases.
SNBL has also developed an intranasal drug-delivery system (N2B-system) that utilizes nose-to-brain technology and is advancing brain disease model research. This approach addresses the challenge of limited drug transfer to the brain and broadens the possibilities for new drug development.
Specific examples include the following projects
SNBL offers efficacy/pharmacology studies using monkey models of glaucoma and age-related macular degeneration, enabling efficient development of new therapeutics for these ocular diseases.
SNBL utilizes nose-to-brain (N2B-system) intranasal delivery to evaluate drug transfer to the brain. This technology enables delivery of agents that do not readily cross the blood–brain barrier, contributing to the development of new drugs for CNS diseases, such as Alzheimer’s disease and Parkinson’s disease, for example.
SNBL is a contract research organization (CRO) that primarily provides support for drug development, offering preclinical testing and drug analysis.
It also develops translational research projects and medical and health-related projects called Medipolis projects. In this way, SNBL supports pharmaceutical companies and medical institutions, contributing to the improvement of medical technology.
| Address | 2438 Miyanoura-cho, Kagoshima City, Kagoshima Prefecture, Japan |
|---|---|
| Tel | 099-294-2600 |
| Website | https://www.snbl.co.jp/ |
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.
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.
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 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.
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.
Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.
Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.
Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.
Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.
Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.
PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.
Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.
Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.