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Abogen Biosciences

Abogen Biosciences is a biopharmaceutical company centered around mRNA technology. While it focuses on developing vaccines and therapeutics through its internal research and development, it also offers external research support functions, as evidenced by its listing on CRO lists in the non-clinical domain. Here, we will introduce the characteristics of Abogen Biosciences and an example of a disease model.

Features of Abogen Biosciences' Non-clinical Testing Contract Services

Integrated platform for consistent support of mRNA drug discovery

Abogen Biosciences is,Owns a proprietary platform covering mRNA drug design, preclinical development, and manufacturingWe are doing this. Unlike typical CROs that are divided by testing stages, our feature is that we can provide integrated mRNA sequence design, formulation development, and evaluation systems. This allows for rapid reflection of validation results from the preclinical stage to the next stage, contributing to improved speed and reproducibility of the overall development. We can provide seamless support from the early stages of drug discovery with clinical transition in mind.

Non-clinical evaluation capabilities specialized in LNP technology and mRNA

with proprietary LNP (lipid nanoparticle) delivery technology as its strengthHigh expertise in non-clinical evaluation addressing unique challenges of mRNA therapeuticsWe have expertise. Specifically, we can handle verification items that differ from conventional small molecule and antibody drugs, such as in vivo distribution and expression characteristics of mRNA, stability of LNPs, and evaluation of immune response and toxicity. Our accumulated knowledge specialized in mRNA allows us to precisely understand the characteristics of candidate compounds, contributing to reduced development risk and increased success rate.

GMP manufacturing base and global regulatory compliance capabilities

We have a large-scale manufacturing facility that complies with GMP standards and a CDMO function that can handle everything from research stages to manufacturing scale. We also have extensive experience in dealing with regulatory authorities in various countries.Achievements such as obtaining Emergency Use Authorization (EUA) in Indonesia and conducting a large-scale international Phase III clinical trial with 30,000 participants.We have established a support system that can design and consult on data with approval applications in mind from the non-clinical stage, which is useful for companies aiming for global development.

An example of a disease model held by Abogen Biosciences

KRAS mutated tumor model

KRAS-mutated tumor models are used to reproduce the frequent KRAS gene mutations in refractory cancers and to evaluate the efficacy of mRNA vaccines and immunotherapies. They are characterized by their ability to analyze tumor growth suppression and immune response induction from multiple angles, and are particularly useful forPreclinical validation of personalized cancer vaccinesIt is suitable. Highly accurate evaluations are possible by considering interactions with the immune system.

Disease-specific mouse model

We conduct non-clinical evaluations utilizing disease-specific mouse models in the fields of infectious diseases and tumors. In the infectious disease field, we use models that can verify immune responses against mutant strains to evaluate the protective efficacy of vaccines and the induction of neutralizing antibodies. In the tumor field, including KRAS mutant models,Systematically verify the mechanism of action and efficacy of cancer immunotherapy.And analysis is being conducted based on the characteristics of mRNA therapeutics.

Abogen Biosciences Non-clinical Trial Cases

Efficacy Study Using a KRAS-Mutated Tumor Model

In preclinical studies using a KRAS-mutated tumor model, we verified the efficacy of our proprietary KRAS mRNA vaccine "ABO2102." Administration to a mouse model showedTumor shrinkage was confirmed with monotherapy.Furthermore, in combination with PD-1 antibodies, potent anti-tumor effects, including tumor eradication, have been reported. Data also showed activation of the immune response, such as increased T cell infiltration into the tumor. These are preclinical cases demonstrating the potential of mRNA vaccines for cancer immunotherapy.

Reference: Abogen Biosciences Official Website
https://abogenbio.com/news/company/news2025/231.html

Abogen Biosciences Corporate Information

Address Building 8, 21 Dongyanli Road, Suzhou Industrial Park, Suzhou, Jiangsu, 215000, China
Tel Not listed
Website https://abogenbio.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
By region
list of animal models
Expertise & Track Record
3 Recommended CRO for Non-Clinical Studies