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Hamamatsu Pharma Research

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Table of Contents

Hamamatsu Pharma Research specializes in non-clinical studies using non-human primates (NHPs).

This page showcases key features of the company’s non-clinical capability, examples of disease models, and case studies.

We hope it serves as a useful reference when you are selecting a non-clinical CRO.

Non-clinical Model Available at Hamamatsu Pharma Research

High-precision pharmacological study using non-human primates (NHPs)

EPHamamatsu Pharma Research specializes in non-clinical models with non-human primates such as crab-eating macaques—the experimental animals most closely related to humans.

By overcoming the limitations of conventional small animal models such as mice, the company has improved the accuracy of efficacy predictions in humans.

These studies are especially reliable in areas where human-like models are essential, including central nervous system (CNS) disorders and rare diseases.

Drug discovery support using unique disease models and the PIT method

In collaboration with Hamamatsu University School of Medicine, the company provides high-precision non-clinical studies utilizing the university’s proprietary “PIT method” and can offer co-development of new model or established disease models.

Their research covers a wide range of disease areas, including exudative and atrophic age-related macular degeneration, osteoarthritis of the knee, anti-tumor drug-induced neuropathic pain, cerebral infarction, and Parkinson’s disease.

Even when a candidate drug shows limited efficacy, the obtained data can provide valuable insights for the future research and development.

Experienced researchers and full ethical accreditation

The company is equipped with teams of specialized researchers with advanced expertise in primate handling and testing.

They offer flexible work flow that allows for last-minute protocol modifications if necessary.

Hamamatsu Pharma Research is fully accredited by AAALAC International standard, ensuring the highest standards of animal welfare, ethics, and safety.

Contract Research Partners of Hamamatsu Pharma Research

No information regarding partnered organizations was found on the official website.

Case Studies of Non-clinical Trials

Pharmacological studies for central nervous system diseases

Hamamatsu Pharma Research focuses on the development of experimental models for focal cerebral ischemia (acute and chronic) and Parkinson’s disease in small animals and monkeys.
For cerebral infarction, they offer middle cerebral artery (MCA) thrombus, permanent occlusion, transient occlusion, and embolization models, which enable quantification of infarct size and functional assessments.
For Parkinson’s disease, available models include the systemic MPTP administration model and the MPTP hemiparkinsonism model.

Reference: Hamamatsu Pharma Research official website
https://www.hpharma.jp/service/pharmacology/central-nervous/

Pharmacological studies for cardiovascular diseases

The company has developed various thrombosis models, including the PIT model (Photochemically Induced Thrombosis).
It can produce mural thrombi through balloon injury and perform quantitative evaluation using diagnostic ultrasound and MRI imaging technologies.

Reference: Hamamatsu Pharma Research official website
https://www.hpharma.jp/service/pharmacology/circulatory/

Company Information

Hamamatsu Pharma Research focuses exclusively on non-clinical pharmacological testing and is actively engaged in research and development within this field.

Address 1-3-7 ShinMiyakoda, Hamana-ku, Hamamatsu City, Shizuoka, Japan
Tel 053-543-4543
Website https://www.hpharma.jp/
3 Recommended Contract Research Organizations for Non-Clinical Studies
— by Target goal and Expertise

In drug discovery, the quality and efficiency of non-clinical studies have a direct impact on clinical success rates, development costs, and overall length of time required in R&D. In recent years, there has been more demand for clinically relevant data, globally accepted reliability, and accurate early-stage screening. Thus, it is more important than ever to select the right CRO (Contract Research Organization) for strategic approach.
In this article, we highlight three CROs with proven technical capabilities, expertise, and long standing track records. These are our TOP 3 choices based on their capabilities and the specific target goals of the researchers for their non-clinical studies.

Pharmacology (Efficacy) Studies
Replicate unknown pathological models and
Discovery to clinically oriented drug evaluation
SMC Laboratories, Inc.
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories, Inc. has established a disease models using patented mouse technologies. The company has established proprietary pathological models—particularly in liver disease and fibrosis—and continues to expand their approach across a wide range of models in cancer, inflammation, and metabolic diseases.
  • From exploratory research to clinically oriented efficacy evaluation, SMC offers customized study designs, dosing strategies, and evaluation analysis tailored to each project. Their collaborative approachallows researchers to discuss and refine study plans together with SMC’s expert scientists.

  • With flexible small-scale study options and strong technical support, SMC Laboratories, Inc. is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
Labcorp Holdings Inc.
(Labcorp Drug Development)
Labcorp Holdings Inc.
Reference: Labcorp Holdings Inc. official website (https://jp.labcorp.com/)
  • Labcorp Holdings Inc. provides a fully integrated GLP testing system aligned with international regulatory standards, including FDA, EMA, and PMDA requirements. All studies are conducted under ICH-compliant quality assurance, making it ready for data submission.
  • The company has extensive expertise in long-term toxicity studies such as Segment I–III reproductive and carcinogenicity studies, as well as 2-year chronic toxicity assessments.
  • Labcorp Holdings Inc.’s comprehensive approach enables sponsors to efficiently outsource the entire preclinical package from toxicology, toxicokinetic (TK), and safety pharmacology study design to execution. This accelerates a path to First-in-Human (FIH) trials. For most of the global drug developers, this all-in-one service structure minimizes cost, risk, and expedite the time before advancing to clinical phase.
Pharmacokinetic (PK/PD) Studies
High-Precision Bioanalysis for Clinically Predictive PK/PD Evaluation
PhoenixBio Co., Ltd.
PhoenixBio Co., Ltd.
Source: PhoenixBio Co., Ltd. Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio Co., Ltd.offers pharmacokinetic and hepatic metabolism studies using their proprietary PXB-mouse®, a humanized-liver chimeric mouse model. This platform enables the acquisition of data with high clinical correlation in ADME, drug–to-drug interaction studies, bridging the gap between preclinical and clinical stages.
  • With advanced LC-MS/MS-based bioanalysis, PhoenixBio Co., Ltd. provides aseamless workflow from plasma concentration measurement and metabolite identification to quantitative validation.

  • The company offersan integrated evaluation analysiscovering pharmacokinetics, hepatotoxicity, and safety with flexibility to accommodate complex modalities such as oligonucleotide and middle-molecule therapeutics. For compounds where hepatic metabolism is a development bottleneck—or where quantitative, reproducible exposure data are critical—PhoenixBio Co., Ltd. delivers unmatched analytical precision and consistency.

By region
list of animal models
Expertise & Track Record
3 Recommended Contract Non-Clinical Testing Services