Nonclinical Efficacy Testing » Non-Clinical CROs and Agencies » Hera BioLabs

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
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— by Target goal and Expertise

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.

Pharmacology (Efficacy) StudiesDisease-Relevant Models for
Translational Drug Evaluation
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/)

SMC Laboratories, Inc.

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.

Areas of Expertise
Disease-Relevant Model Portfolio

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 Design Based on Target Biology

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.

Support from Target Validation to Proof of Concept

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.

Safety StudiesComprehensive Safety Assessment for
Preclinical Development
Charles River Laboratories
Reference: Charles River Laboratories official website (https://www.criver.com/)

Charles River Laboratories

Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.

Areas of Expertise
General Toxicology Across Study Designs

Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.

Non-GLP and GLP Study Support

Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.

Integrated IND-Enabling Safety Assessment

Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.

Pharmacokinetic (PK/PD) StudiesConnecting Drug Exposure with
Pharmacological Response
Inotiv
Reference: Inotiv official website (https://www.inotiv.com/)

Inotiv

Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.

Areas of Expertise
Pharmacokinetic Characterization

PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.

Exposure–Response Evaluation

Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.

Integrated DMPK and Development Support

Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.

By Therapeutic Area
Disease Animal Models
and Reviews
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