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Jubilant Biosys

Table of Contents
Table of Contents

Jubilant Biosys is a Contract Research and Manufacturing Organization (CRMO) that provides integrated services from early drug discovery to preclinical studies for global pharmaceutical and biopharmaceutical companies. With bases in India and Europe, we contribute to the creation of innovative therapeutics through high-quality research and development support.

Here, we will introduce in detail Jubilant Biosys' strengths in non-clinical studies, examples of disease models they possess, and specific use cases.

Jubilant Biosys' Contract Non-Clinical Testing Services Features

Addressing a wide range of disease areas

One of Jubilant Biosys's features is its ability to address a wide range of disease areas, including cancer, central nervous system disorders, metabolic diseases, pain, and inflammation. At its advanced research facilities in India and France,in vitroandin vivoWe offer a wide range of non-clinical testing services, from pharmacology studies to drug metabolism and pharmacokinetics (DMPK) studies, and GLP and non-GLP toxicology studies, flexibly meeting the diverse drug discovery needs of our customers.

An integrated approach with comprehensive facilities

Another key feature is our integrated approach, leveraging comprehensive facilities and advanced expertise. Our experienced team of scientists utilize high-performance infrastructure to deliver high-quality data, supporting rapid decision-making from the early stages of development. We go beyond simple contract testing; as a CRDMO, we offer end-to-end support, from identifying drug discovery targets to preclinical testing and even the scale-up manufacturing of active pharmaceutical ingredients, thereby facilitating a more efficient drug discovery process.

An example of a pathological model held by Jubilant Biosys

Diversein vivoPathological model

The company offers a wide range of [products/services] to thoroughly evaluate complex disease mechanisms.in vivoI own animal models.

Representative examples include pain models that evaluate chemotherapy-induced allodynia and bone cancer pain, and skin disease models for contact dermatitis and psoriasis. In addition, "metabolic disease models," including diabetes, are well-developed, supporting the efficacy evaluation of new drug candidate compounds with study designs tailored to the characteristics of each disease.

Reference: Jubilant Biosys Official Website
https://www.jubilantbiosys.com/services/in-vivo-pharmacology/

Advanced oncology models

For cancer, a key focus area, we offer a rich selection of proprietary, advanced oncology models. Specifically, evaluation systems utilizing a wide variety of cancer cell lines, including pancreatic, lung, and breast cancer, are available. By leveraging these models, which are based on past research trends, we can meticulously validate the efficacy and mechanisms of action of anticancer drugs, thereby supporting efforts to accelerate and achieve success in the development of innovative pharmaceuticals in the field of oncology.

Jubilant Biosys's Non-Clinical Study Cases

Due to the nature of being a CRDMO, strict confidentiality agreements (NDAs) are in place, and details of individual drug discovery program support are not publicly disclosed on our website. For approaches to specific disease targets or detailed case studies, please contact us directly to receive information disclosure or proposals tailored to your requirements.

Jubilant Biosys also supports the non-clinical studies of its sister company, Jubilant Therapeutics. The following are case studies featured in Jubilant Therapeutics' public disclosures.

New anti-cancer drug non-clinical study cases

We conducted non-clinical studies on "JBI-778," a novel PRMT5 inhibitor candidate for anti-cancer drugs. This compound isin vitroIn addition to demonstrating antitumor activity in preclinical studies, oral administration achieved greater than 90% tumor growth inhibition in a mouse Z-138 xenograft model%.

Furthermore, sustained exposure and substantial survival extension in the brain have been confirmed in a glioblastoma (GBM) model of the same location, showing promising data as a clinical candidate.

Jubilant Biosys Company Information

Jubilant Biosys is a global company that seamlessly supports early drug discovery research through to commercial production. Leveraging its infrastructure and expertise, it holistically supports its customers' drug development.

Address India (Bengaluru, Noida, Greater Noida), France (Saint-Julien-en-Genevois)
Tel +91 120 436 1000 (Representative of Head Office in India)
Website https://www.jubilantbiosys.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