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Preclinical Oncology CRO Services
Cyagen provides end-to-end oncology CRO services – from advanced animal models to comprehensive drug evaluation and translational insights. Our platform accelerates oncology research with customizable models and validated preclinical solutions.
One-Stop Oncology CRO Solutions
As one of the leading preclinical oncology CRO companies, Cyagen provides comprehensive preclinical CRO solutions for oncology drug evaluation, supporting antibody drugs, cell and gene therapies, mRNA-based approaches, and more. Our platform covers the full workflow — from diverse tumor model generation (CDX, PDX, GEM, syngeneic, humanized) to in vivo efficacy studies and in vitro mechanistic assays. With extensive experience across 200+ oncology projects and support for IND applications, we help biopharma teams accelerate their oncology pipelines with confidence and precision.
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Cyagen delivers comprehensive in vivo efficacy evaluation services that simulate clinical settings with high fidelity. From tumor establishment to pharmacodynamic monitoring, our platform supports a wide spectrum of model types and therapeutic modalities—helping clients generate robust, IND-enabling preclinical data.
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Need Customized Evaluation for Your Therapy?
If your desired neuroscience model isn’t listed, our experts are here to help! Request a Custom Animal Model >>
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At Cyagen, we offer advanced in vivo drug delivery and phenotyping services tailored for ophthalmic studies. From precise ocular injections to high-resolution imaging and vision behavior analysis, our platform provides comprehensive capabilities to evaluate drug efficacy and safety. Supported by expert personnel and cutting-edge instrumentation, we ensure consistent, accurate, and reproducible preclinical results.
Customized Study Design
Designs tailored for evaluating mAbs, mRNA drugs, CAR-T/NK therapies, oncolytic viruses, and immune checkpoint inhibitors.
  • IND-ready timelines & professional consultation included.
Tumor Model Flexibility
Supports subcutaneous, orthotopic, hematologic, and metastatic tumor models using:
  • CDX (Cell-Derived Xenograft)
  • PDX (Patient-Derived Xenograft)
  • GEMM (Genetically Engineered Mouse Models)
  • Humanized Immune Mouse Models (e.g., huHSC-C-NKG-ProF)
Endpoints & Technologies
  • Tumor volume, body weight, survival
  • ging (bioluminescence/fluorescence)
  • Flow cytometry, H&E, IHC, ELISA, qPCR
  • Customized readouts for mechanism-of-action or resistance studies
Need Customized Evaluation for Your Therapy?
Request In Vivo Drug Testing →
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Cyagen offers a full suite of in vitro and ex vivo pharmacology services to support oncology drug discovery and mechanistic studies. These assays complement in vivo models, providing high-throughput, reproducible insights into drug cytotoxicity, immune act
Cytotoxicity & Immune Function Assays
  • LDH / CTG / CCK-8 viability and cytotoxicity tests
  • CAR-T/NK-mediated cell killing & activation
  • T/NK cell cytokine secretion and proliferation
  • Antibody-dependent cellular cytotoxicity (ADCC)
Molecular & Biomarker Detection
  • Western Blot, ELISA, qPCR for expression profiling
  • Cytokine panels via Singleplex (ELISA) and Multiplex (Luminex, MSD, FACS CBA)
  • DNA/RNA detection via digital PCR and molecular hybridization
Histology & Imaging-Based Analysis
  • H&E staining, immunohistochemistry (IHC)
  • Immunofluorescence (IF), dual/multiplex labeling
  • Fluorescence imaging for tissue localization & distribution
  • In vivo biodistribution via IVIS if applicable
Pharmacokinetics & Toxicity (Optional add-on)
  • Single or repeat dose toxicity testing
  • Genotoxicity, reproductive toxicity, carcinogenicity
  • Blood chemistry, organ indices, LC-UV bioanalysis
Looking to Validate Drug Mechanisms or Biomarkers?
Request In Vitro & Molecular Assays →
Case Examples
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Our Unique Advantages
Broad Model Coverage for Translational Relevance
Cyagen provides one of the industry’s most extensive tumor model libraries—ranging from CDX, PDX, GEMM, to fully humanized immune mice—enabling clinically relevant assessments for diverse oncology pipelines.
End-to-End Evaluation from Efficacy to Mechanism
From tumor growth curves to biomarker analysis, we support every stage of your study with comprehensive endpoints—IVIS imaging, survival tracking, histology (H&E/IHC), qPCR, flow cytometry, and more.
Proven Success in IND-Enabling Projects
With 200+ oncology studies completed and multiple IND applications supported, our CRO platform combines validated workflows with expert guidance to accelerate your drug development with confidence.
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Request a Preclinical CRO Services Consultation
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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