HAMRI is a GLP contract research organization (CRO) offering non-clinical study for pharmaceutical and regenerative medicine, fully AAALAC-accredited facilities.
The company has extensive expertise in various disease models and strong capabilities in providing support from the study design stage.
HAMRI undertakes all three core areas of non-clinical testing—pharmacodynamic studies, safety studies, and pharmacokinetic studies—in-house.
The company conducts efficacy evaluations in various animal models in diabetes, autoimmune diseases, and Parkinson’s disease.
Under GLP compliance, HAMRI also performs safety evaluations including toxicity and genotoxicity studies, as well as pharmacokinetic analyses of absorption, distribution, metabolism, and excretion (ADME).
With an integrated system that covers study design, data analysis, and report preparation, they offer flexible and tailored design for clients’ needs.
In addition to being fully GLP compliant, they are also fully accredited by AAALAC International, a global organization that evaluates and certifies laboratory animal care.
By combining scientific reliability with animal welfare, HAMRI has earned the trust of regulatory authorities and pharmaceutical companies both in Japan and globally.
They continue to implement various protocols to ensure high-quality and safe testing environment.
HAMRI provides a broad selection of animal models for various diseases, including STZ (streptozotocin)-induced Type I diabetes models.
They deliver highly accurate efficacy evaluations for specific disease targets.
In the diabetes model, they offer multifaceted evaluation parameters— change in blood glucose levels, insulin secretion level—which allow detailed verification of the efficacy and mechanism of action of candidate compounds.
HAMRI has Type I diabetes mellitus model in crab-eating monkeys.
This model is induced by streptozotocin (STZ), which is used for pharmacological efficacy studies.
As a diabetes model, detailed efficacy evaluations can be conducted based on multiple indications, changes in blood glucose and insulin secretion level.
They can also co-develop a long-term exploratory study with the same animal for prolonged period of time.
You can expect gaining valuable data for drug discovery or investigating disease mechanism of action. Standard analysis includes sample analyses using ELISA, real-time PCR, and FACS.
Reference:
https://www.hamri.co.jp/medicinal-effect
HAMRI have developed STZ-induced Type I diabetes model in micromini pigs. They measure blood glucose levels over time.
In this study, a continuous glucose sensor was implanted subcutaneously to track the progression of diabetes in real time, demonstrating an innovative evaluation approach for new diabetes models that contributes to drug discovery research.
This is a valuable case study from HAMRI’s. It was recorded through an external presentation.
Reference:
https://www.hamri.co.jp/seminar02
| Address | 2638-2 Osaki, Koga City, Ibaraki Prefecture, Japan |
|---|---|
| Tel | 0280-76-4477 |
| Website | https://www.hamri.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.