Shikoku Rika is a contract research organization (CRO) focused on nonclinical pharmacokinetic studies using radiolabeled compounds. This overview presents the characteristics of Shikoku Rika’s nonclinical studies, an example disease model, and representative case studies. It is intended as a reference when selecting a CRO for nonclinical studies.
Shikoku Rika conducts core ADME studies utilizing radiolabeled compounds (e.g., 14C, 3H) and maintains technologies that enable prediction of clinical-dose pharmacokinetics from early stages of drug discovery and development. Strengths include microdose studies and microtracer studies using stable-isotope tracer methods. In addition to study designs aligned with international standards (FDA, ICH), advanced analytical platforms such as Accelerator Mass Spectrometry (AMS) are implemented to quantify drugs at low concentrations. Comprehensive evaluation of chemical substances is supported, from safety testing of pharmaceuticals and agrochemicals to metabolite identification.
In collaboration with universities and research institutions, Shikoku Rika conducts nonclinical studies using genetically engineered mice. The organization maintains neurodegenerative disease models (in partnership with QPS, Austria) and iPS cell–derived teratoma evaluation models. Expertise also includes antitumor efficacy studies using cancer cell transplantation models (subcutaneous, organ, and intracerebral implantation). End-to-end services are offered—from creation of genome-edited animals using CRISPR/Cas9 technology through phenotypic analysis. The proprietary PXB mouse (a human hepatocyte–repopulated model) enables assessment of human-relevant drug metabolism.
Shikoku Rika’s contracted service for drug efficacy evaluation employs a COPD mouse model generated by exposing C57BL/6 mice to mainstream tobacco smoke for three months using a tobacco smoke inhalation device, followed by efficacy assessment.
Anhyo Center conducts contracted studies on the safety of chemical substances—primarily pharmaceuticals and agrochemicals—and provides contract production of genetically engineered mice, sales of model mice, and contracted nonclinical studies using the produced models. As the Japan distributor for QPS (Austria), the company offers contracted Non-Clinical studies that utilize QPS’s genetically engineered animal models of neurodegenerative disease.
TransGenic is a CRO specializing in nonclinical studies that employ genetically engineered animals. The company’s core capability is the creation of genome-edited mice using CRISPR/Cas9 technology (knockout/knock-in/transgenic), and it supplies disease models such as Parkinson’s disease and diabetes. Drug efficacy evaluations are conducted at GLP-compliant facilities using central nervous system (CNS) and metabolic disease models, supporting programs from early discovery through transition to clinical trials. Leveraging high human-relevance PXB mice and proprietary disease-visualization technology, TransGenic can generate data aligned with international standards (FDA/ICH).
For Shikoku Rika’s contracted service evaluating drug efficacy using COPD model mice, Funakoshi collaborates by supplying the Shibata Kagaku SG-300 Tobacco Smoke Generator and the Tobacco Smoke Exposure Chamber. Using the supplied equipment, C57BL/6 mice are exposed to tobacco mainstream smoke for three months to establish a COPD model. This approach shortens the typical six-month model-creation period and yields models with pronounced alveolar wall destruction. The resulting models exhibit neutrophil dominance in bronchoalveolar lavage fluid (BALF) and are suitable for efficacy evaluation in COPD research.
APPosk-Tg mice exhibit multiple Alzheimer’s disease pathologies, including synaptic loss, abnormal tau phosphorylation, glial activation, and neuronal death. The model supports the oligomer hypothesis in which Aβ oligomers drive Alzheimer’s pathology and can be used to study therapeutics that target these mechanisms.
Based on the hypothesis that impaired processing of proBDNF to mature BDNF contributes to psychiatric and neurological disorders, a knock-in mouse carrying a processing-suppressing mutation was created. Behavioral testing in this model is used to study depression and other psychiatric and neurological conditions.
To investigate the role of IL33 in skin, a transgenic mouse expressing the IL33 gene under the control of a skin-specific keratin-14 promoter was generated. From eight weeks of age, all mice naturally developed atopic dermatitis, supporting a mechanism in which increased eosinophils contribute to disease onset.
Since its establishment in 1979, Shikoku Rika has been committed to the development of the life science research field in the four prefectures of Shikoku. The company conducts contracted non-clinical studies using genetically engineered mice.
| Address | 1067-6 Otsu Otsu, Kochi City, Kochi Prefecture |
|---|---|
| Tel | 088-866-5000 |
| Website | https://www.shikokurika.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.