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CRO Solutions for Metabolic Diseases
Cyagen offers comprehensive CRO solutions to accelerate your research in metabolic diseases. From diverse, validated disease models to robust in vivo and in vitro platforms, we provide end-to-end support, guiding your projects seamlessly from early discovery to IND application. Partner with us to advance your therapeutic breakthroughs.

Integrated CRO Solutions for Metabolic Disease Drug Development

Cyagen provides end-to-end preclinical CRO solutions for metabolic disease research and therapeutic development. Our capabilities include validated animal models and customized in vivo and in vitro studies for obesity, diabetes, dyslipidemia, metabolic dysfunction-associated steatotic liver disease (MASLD/MASH), and metabolic kidney disorders. From disease model selection and mechanism-of-action studies to efficacy, pharmacodynamic, and IND-enabling research, our integrated platforms help researchers generate reliable translational data and advance metabolic drug candidates toward clinical development.
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Ready-to-Use Metabolic Disease Models

Accelerate metabolic disease research with Cyagen’s in stock animal models and standardized modeling kits. Our portfolio supports studies in obesity, diabetes, dyslipidemia, MASLD/MASH, and metabolic kidney disorders, with genetically engineered models, diet-induced models, and chemically induced disease systems. Researchers can select validated off-the-shelf models for rapid study initiation or use optimized modeling kits to establish reproducible disease phenotypes in suitable mouse or rat strains. Cyagen also provides model selection guidance based on the therapeutic target, mechanism of action, disease stage, and required study endpoints.
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Custom Induction-Based Models

In addition to our genetic model library, Cyagen offers a collection of induction-based models developed through established experimental protocols. Beyond our standard MouseAtlas™ catalog, Cyagen offers a robust portfolio of fully validated, induction-based models exclusively through our custom CRO services. These models are ideal for studies requiring clinical-like disease phenotypes that cannot be fully recapitulated by gene-edited lines alone.

Available Models Include

Related Diseases Modeling Method Strain Background
Obesity and Prediabetes High-Fat Diet (HFD)-Induced Mouse & Rat
Diet-Induced Obesity (DIO) Mouse
Type 2 Diabetes STZ plus HFD-Induced Mouse
Zucker Diabetic Fatty (ZDF) Rat
Type 1 Diabetes Streptozotocin (STZ)-Induced Mouse
Sarcopenia Dexamethasone-Induced Mouse
MASLD and MASH Diet-Induced Obesity (DIO) Mouse
DIO plus CCl₄-Induced Mouse
Gubra-Amylin NASH Diet plus CCl₄-Induced Mouse
Liver Fibrosis CCl₄-Induced Mouse
Acute Kidney Injury Acetaminophen (APAP)-Induced Mouse
Polycystic Kidney Disease Induced Mouse
INTEGRATED PRECLINICAL CAPABILITIES
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Metabolic Disease Phenotyping and Efficacy Readouts

Our in vivo CRO platform delivers customized efficacy evaluation for metabolic drugs. From glucose tolerance and lipid profiling to liver pathology, we help generate data aligned with clinical endpoints.
Obesity and Diabetes Phenotyping
  • Body weight monitoring
  • Fasting and random blood glucose measurement
  • Metabolic cage analysis
  • Assessment of obesity- and diabetes-related metabolic parameters
Metabolic Pharmacology Pilot Studies
  • Conditioned taste aversion studies
  • Gastric emptying tests
  • Acute food intake studies
  • Glucose tolerance tests (GTT)
  • Insulin tolerance tests (ITT)
Liver and Pancreas Evaluation
  • Liver weight and tissue volume quantification
  • Serum liver enzyme analysis, including ALT and AST
  • Histopathological analysis using H&E, Oil Red O, Sirius Red, and immunohistochemistry
  • Assessment of hepatic steatosis, inflammation, and fibrosis
  • Evaluation of pancreatic edema and tissue injury
  • Observation and quantification of saponification spots in acute pancreatitis models
Kidney Function and Injury Assessment
  • Urine volume, protein, and glucose analysis
  • Glomerular filtration rate (GFR) assessment
  • Blood urea nitrogen (BUN) and serum creatinine measurement
  • Renal inflammatory and fibrotic biomarker analysis, including TGF-β1 and IL-6
  • Histopathological assessment of renal tissue injury
  • Evaluation of kidney function and disease progression using renal injury biomarkers
INTEGRATED PRECLINICAL CAPABILITIES
Looking for tailored in vivo assays to validate your candidate?

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In Vitro Target Validation & Mechanistic Studies
Our in vitro platform supports target validation and mechanism-of-action studies for metabolic drug development using disease-relevant cellular models, biochemical assays, and biomarker profiling.
Target-Based Drug Screening
  • PPAR-α/γ activity assays
  • 11β-HSD inhibition assays
  • GLP-1R functional assays
  • DPP-IV activity and inhibition assays
Metabolic Biomarker Profiling
  • Adipokines and metabolic hormones, including leptin, GIP, GLP-1, resistin, and ghrelin
  • Multiplex cytokine detection using MSD, Luminex, and ELISA
Cellular Models for Mechanism-of-Action Studies
  • INS-1 and MIN6 pancreatic β-cell models
  • HK-2 renal epithelial cells and mesangial cells
  • Primary hepatocytes and adipocyte models
  • Glucose transporter uptake and cAMP signaling assays
INTEGRATED PRECLINICAL CAPABILITIES
Need support for in vitro screening or mechanistic insights?

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Case Studies
Key advantages
Broad Model Coverage with Clinical Relevance
From classic ob/ob and Apoe KO models to inducible MASH and PAH systems, our platform supports both genetic and induction-based disease models to match diverse drug discovery needs.
Integrated In Vivo & In Vitro Evaluation Systems
Our end-to-end services cover behavioral testing, blood biochemistry, histology, molecular assays, and target engagement studies—empowering complete pharmacodynamic insights in metabolic and cardiovascular indications.
Proven Experience in Translational Research
With 200+ successful projects and validated data for IND-enabling studies, we provide reliable support for preclinical efficacy assessment and customized model development for metabolic and cardiovascular drug pipelines.
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Partner with Cyagen to advance your preclinical studies. Share your project goals with us and receive customized support.
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Global Antibody Drug Industry Development BlueBook (Frost & Sullivan)
Key Insights
The industry is undergoing a rapid transformation driven by next-generation modalities, globalized markets, and upstream technological innovations.
  • Market Structural Shift: Monoclonal antibodies drive steady growth, but ADCs and bispecifics are rapidly accelerating, reshaping the market with higher-value innovations.
  • Chinese Market Globalization: China is actively expanding globally, evidenced by a surge in high-value cross-border license-out deals.
  • Technology-Driven Efficiency: Advanced discovery engines—exemplified by Cyagen's HUGO-Ab platform and AI algorithms—are streamlining candidate screening, optimizing molecular design, and localizing the upstream supply chain.
  • Oncology-Focused Innovation: R&D pipelines remain heavily concentrated on high-incidence malignancies like non-small cell lung cancer, utilizing complex modalities to combat clinical resistance.
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