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).
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.
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.
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.
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.
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.
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.
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.
No case studies are currently listed on the official website.
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/ |
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.