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Hera BioLabs

Table of Contents
Table of Contents

Hera BioLabs is a US-based Contract Research Organization (CRO) that offers testing services utilizing its proprietary gene editing technology and high-quality disease model rats. This article will provide a detailed explanation of the features of the company's services and the models it possesses. Please use this as a reference when choosing a partner to accelerate your research and development.

Features of Hera BioLabs' Non-clinical CRO Services

High-precision data acquisition with proprietary "SRG Rat"

Hera BioLabs' most distinctive feature is its testing using the in-house developed immunodeficient rat, the "SRG Rat." These rats have metabolic functions closer to humans than mice and boast high engraftment rates, allowing for data with high clinical predictability.

The fact that a large size allows for the collection of many samples from a single individual, enabling efficient analysis, is also a significant advantage, wouldn't you agree?

Flexible customization with advanced gene editing technology

Our strengths also include flexible responses utilizing proprietary gene editing technologies such as "Cas-CLOVER" and "piggyBac." These enable precise genetic modifications with extremely low off-target mutations.

You can use it with peace of mind because we can create custom models tailored to your needs and the commercial use rights are clear.

An example of a disease model held by Hera BioLabs

SRG Rat (OncoRat) Specialized in Oncology Research

SRG Rat (commonly known as OncoRat) is a severely immunodeficient rat with knockout Rag2 and Il2rg genes. It lacks B cells, T cells, and NK cells, and boasts a high engraftment rate even for human cancer cells (such as VCaP) that are difficult to engraft in mice.

Because the tumor grows large, an abundant tissue sample can be obtained in a single test, allowing for detailed pathological analysis.

"Humanized SRG Rat Model" with a Reconstituted Immune System

This is a model where human peripheral blood mononuclear cells (PBMCs) and hematopoietic stem cells are engrafted into SRG rats, thereby reconstituting the human immune system. This model allows for the evaluation of the efficacy of cancer immunotherapies (such as checkpoint inhibitors).

Rats are a significant advantage because they have a large blood volume, allowing for blood collection from the same individual over time to monitor changes in immune cell dynamics in detail.

Hera BioLabs Preclinical Case Studies

Improved engraftment rate in prostate cancer (VCaP) models

This is a case study using the human prostate cancer cell line "VCaP," which has a low engraftment rate and heterogeneous growth in immunodeficient mice. When tested using Hera BioLabs' SRG Rat, high engraftment rates of over 90%and uniform tumor growth were confirmed.

Additionally, by utilizing the large blood volume in rats and measuring serum PSA concentration over time, a high correlation with tumor volume has been demonstrated.

Establishment and serial transplantation of patient-derived xenograft (PDX) models

Here are examples of PDX models using patient-derived tissues for non-small cell lung cancer (NSCLC) and other conditions. SRG Rats show faster tumor growth compared to NSG mice, allowing for shorter study durations.

Furthermore, it has been shown that because the tumor grows large, many tissue fragments (PDX banks) can be secured in a single transplant, and serial transplantation to the next generation can also be performed efficiently.

Hera BioLabs Company Information

Hera BioLabs is a US-based Contract Research Organization (CRO) that offers its proprietary gene editing technology and high-performance immunodeficient "SRG Rat." We accelerate cancer research and drug discovery processes with innovative technologies and flexible responsiveness.

Address 2277 Thunderstick Drive, Suite 500, Lexington, KY 40505, USA
Tel +1 859-414-0648
Website https://www.herabiolabs.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