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Champions Oncology

Champions Oncology is a CRO specializing in oncology with over 1400 patient-derived cancer models. Champions Oncology conducts contract non-clinical studies using proprietary models for everything from early-stage drug discovery to immuno-oncology. This section summarizes the features of the company's contract non-clinical study services, its disease models, and examples of non-clinical studies.

Features of Champions Oncology's Contract Non-clinical Trial Services

Unique workflow dedicated to early drug discovery services

The company specializes in two types of early drug discovery services to provide highly reliable data and cost-effective solutions quicklyProvides a uniquely integrated workflowThe company's two main products are "ChemiSelect" and "ADC-Flow". ChemiSelect" is a platform developed to effectively identify and prioritize chemotypes, while "ADC-Flow" is a platform for screening and designing efficient antibody-drug conjugates (ADCs) for client targets.

Various evaluations can be performed in mouse clinical trials

The company's Mouse Clinical Trials (MCTs) can use patient-derived cancer models implanted in immunocompromised mice to evaluate efficacy against a variety of tumor types and to investigate resistance mechanisms and optimize drug combinations.

Also, the company's MCT design is,Customized to the client's research objectivesWe can do this. Therefore, from model design to study design and final analysis, the company's experts will work with the client to ensure that the study meets its objectives.

Provides a humanized mouse tumor model

The company offersProviding humanized mouse tumor models specific to human immune targetsto support preclinical immuno-oncology research. The platform enables the evaluation of the efficacy and mechanism of action of a wide variety of cancer drugs that modulate human immunity, including checkpoint inhibitors, monoclonal and bispecific antibodies, cancer vaccines, cytokine therapies, and combination therapies.

An example of Champions Oncology's disease model

The company covered molecular and pathologic diversity across major cancer types,Over 1,400 PDX models in our portfolioThe results of this study are shown in Figure 1. These models have been established from biopsy tissue taken from patients with advanced cancer and pretreated with novel therapies. The pretreated PDX models are highly clinically relevant in elucidating resistance mechanisms in cancers that have progressed after standard therapy and in the search for new targets and therapeutic strategies.

Champions Oncology's Non-clinical Case Studies

A case study of the use of the PDX model bank for prostate cancer

Amgen to evaluate AMG160, a PSMA-targeted BiTE molecule with a long half-life,Leveraging Champions Oncology's Prostate Cancer PDX Model BankThe patient was treated with AMG160. In this case, AMG160 is being evaluated in combination with other immunotherapies that reactivate the immune system.

Referenced from: Champions Oncology official website (https://www.championsoncology.com/2023-case-study-using-champions-prostate-pdx-models-for-preclinical-) validation-of-a-novel-psma-directed-bite)

Champions Oncology Company Information

Champions Oncology is a provider of advanced technologies and products for the development and patient-tailored use of oncology drugs. In particular, the company utilizes patient-derived tumor models to provide personalized services to pharmaceutical and biotech companies.

AddressOne University Plaza, Suite 307 HACKENSACK, NJ 07601 USA
Tel201 808-8400
Websitehttps://www.championsoncology.com
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 official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories 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 is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
labcorp
(Labcorp Drug Development)
labcorp
Reference: labcorp official website (https://jp.labcorp.com/)
  • labcorp 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’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
PhoenixBio
Source: PhoenixBio Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio 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 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 delivers unmatched analytical precision and consistency.

Consult Phoenix Bio for PK/PD analysis with a clinical focus