AntiCancer Japan, Inc. is a contract research organization (CRO) specializing in non-clinical studies in oncology. By utilizing proprietary tumor models and bioluminescence technologies, they offer flexible efficacy evaluations in non-GLP environments. Their strength is in pharmaceuticals and regenerative medicine products.
AntiCancer Japan, Inc. focuses exclusively on oncology-related non-clinical research. They offer a wide range of tumor models, including CDX (cell line-derived xenograft) and PDX (patient-derived xenograft) models, to provide practical data for therapeutic drug candidates.
In addition, the company can accommodate flexible design and advanced analytical items, such as luminescence and fluorescence imaging–based monitoring, combination therapy, and tumor relapse models. They have the platform that satisfies the quality and timely execution that are essential to oncology drug development.
Their research facilities are non-GLP (not compliant with Good Laboratory Practice). They have greater flexibility in exploratory research and early-stage screening.
In the early phases of drug development, flexibility and speed are often critical. AntiCancer Japan, Inc. conducts all of their studies in-house. This enables direct communication with researchers to design customized studies and models tailored to specific needs. Their strength lies on the ability to conduct trials and exploratory studies that may be difficult in GLP-compliant environments, especially during the initial developmental stage.
Rather than a large-scale organization,AntiCancer Japan, Inc. maintains a compact team of highly specialized professionals. This allows close communication and personalized support to each client.
After a thorough consultation with the client for their target goals and study requirements, the team fine-tunes study models and protocols accordingly.
With extensive expertise specifically in oncology, the company can provide practical, experience-based advice, which may be hard to find in general-purpose testing facilities. AntiCancer Japan, Inc. serves as a collaborative partner that offers companion-style contract services, working alongside clients to find the best, tailor-made solutions beyond standard protocols.
The CDX model is a standard tumor model induced by transplanting human cancer cell lines subcutaneously or into organs of immunodeficient mice.
Leveraging its advanced oncology expertise, AntiCancer Japan, Inc.offers a wide variety of human cancer cell lines. Researchers can select the most suitable model for each cancer type, including solid tumors and leukemia.
The CDX model offers high reproducibility in tumor growth rate and drug responsiveness and is applicable to various studies, including efficacy evaluation of anticancer drugs, combination therapies, and comparison of administration routes. They can also do real-time monitoring through luminescence and fluorescence imaging with precise quantitative evaluation of treatment.
Reference: AntiCancer Japan, Inc. official website (http://www.anticancerjapan.com/research/index.html)
AntiCancer Japan, Inc. uses tumor cells that express fluorescent and luminescent proteins to visualize tumor formation and treatment effects in mice. This imaging system enables non-invasive, time-course evaluation of tumor regression and regrowth following treatment.
The technique is applicable not only to subcutaneous tumor models but also to tumors implanted in the abdominal cavity, bladder, brain, liver, lungs, bone, and other organs, allowing dynamic observation across various cancer types.
Reference: AntiCancer Japan, Inc. official website (http://www.anticancerjapan.com/research/index.html)
| Address | 2-23-5 Ryukakujidai, Sakae-machi, Inba-gun, Chiba, Japan |
|---|---|
| Tel | 0476-77-8555 |
| Website | http://www.anticancerjapan.com/index.html |
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.