Nonclinical Efficacy Testing » Non-Clinical CROs and Agencies » Anpyo Center

Anpyo Center

Table of Contents
Table of Contents

Effective October 1, 2024, Shinyaku Research Center, Inc. and Anpaku Center, Inc. merged, and the merged entity changed its name to TransGenic, Inc.

Below is a description of the pre-merger information.

Anpyo Center conducts a variety of pharmacological studies related to cardiovascular, allergy, anti-fatigue, and other therapeutic effects.
This section introduces the features of Anpyo Center’s non-clinical pharmacology services, examples of disease models, and related case studies.
Please use this information as a reference when selecting a contract research organization (CRO).

Features of Anpyo Center’s Non-Clinical Testing Services

Extensive Testing Experience

With over 40 years of experience, we have evaluated a wide range of disease models using genetically engineered mice and rats.
Every year, we conduct studies for more than 1,000 clients on diseases such as Parkinson’s disease and myocardial infarction, providing reliable and reproducible data.
Our trusted expertise allows us to support pharmaceutical companies and research institutions seamlessly from early-stage development to clinical trials.

Clear and Supportive Communication

We explain all study details with transparency, easy-to-understand language, minimizing technical misunderstanding.
Our policy is to provide thorough explanations of study objectives, procedures, and expected outcomes, ensuring confidence for clients with no prior non-clinical studies.

One-Stop Service

Our in-house facilities also support environmental toxicity testing. With a wide variety of studies available under one roof, all necessary tests can be completed with a single partner.

Examples of Disease Models at Anpyo Center

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.

SCP-Induced Mouse Model

This model is used to evaluate learning and memory functions in the central nervous system.
Abnormal behaviors induced by SCP, a muscarinic anticholinergic agent, are considered to represent memory impairment in animals and are used as a preclinical indication to identify compounds that improve brain function.

Accelerated Aging Mouse Model

This lineage-specific model exhibits various aging-related disorders similar to those seen in humans, such as amyloidosis, senile osteoporosis, and learning and memory impairment.
It is widely used to study the biological mechanisms of aging, the onset of age-related diseases, and potential prevention or treatment strategies.

Middle Cerebral Artery Occlusion (MCAO) Model

We offer mice, rats, and monkeys as experimental models of stroke for developing new drugs targeting the acute phase of cerebral infarction.
Neurological symptoms, infarct formation, and changes in cerebral blood flow are observed and measured.

Examples of Non-Clinical Studies at Anpyo Center

No case studies are currently listed on the official website.

Company Information

Anpyo Center provides contract pharmacological studies for cardiovascular, allergy, anti-fatigue, and other therapeutic effects, as well as pharmacodynamic equivalence studies for generic drugs.

Address 582-2 Shio-shinden, Iwata City, Shizuoka Prefecture
Tel 0538-58-1266
Website https://www.anpyo.co.jp/

3 Recommended Contract Research Organizations
for Non-Clinical Studies
— by Target goal and Expertise

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
Translational Drug Evaluation
SMC Laboratories, Inc.
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
Preclinical Development
Charles River Laboratories
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
Pharmacological Response
Inotiv
Reference: Inotiv official website (https://www.inotiv.com/)

Inotiv

Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.

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.

By Therapeutic Area
Disease Animal Models
and Reviews
Proven Capability, Expertise and Track Record
Top 3 Non-Clinical CRO Services