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In Vitro

Boost oncology drug discovery with XenoBase®, featuring the largest cell line selection and exclusive 3D organoid models. Benefit from OrganoidXplore™ and OmniScreen™ for rapid, in-depth analysis.

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In Vivo

Enhance drug development with our validated in vivo models, in vitro/ex vivo assays, and in silico modeling. Tailored solutions to optimize your candidates.

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Harness your data and discover biomarkers with our top bioinformatics expertise. Maximize data value and gain critical insights to accelerate drug discovery and elevate projects.

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Accelerate innovative cancer treatments with our advanced models and precise drug screening for KRAS mutations, efficiently turning insights into clinical breakthroughs.

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Advance translational pharmacology with our diverse pre-clinical models, robust assays, and data science-driven biomarker analysis, multi-omics, and spatial biology.

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Our suite integrates preclinical solutions, bioanalytical read-outs, and multi-omics to uncover drug resistance markers and expedite discovery with our unique four-step strategy.

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Enhance treatments with our human tumor and mouse models, including xenografts and organoids, for accurate cancer biology representation.

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Apply the most appropriate in silico framework to your pharmacology data or historical datasets to elevate your study design and analysis, and to improve your chances of clinical success.

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Integrate advanced statistics into your drug development projects to gain significant biological insight into your therapeutic candidate, with our expert team of bioinformaticians.

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CRISPR/Cas9

Accelerate your discoveries with our reliable CRISPR solutions. Our global CRISPR licenses cover an integrated drug discovery platform for in vitro and in vivo efficacy studies.

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Gain more insights into tumor growth and disease progression by leveraging our 2D and 3D fluorescence optical imaging.

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Mass Spectrometry-based Proteomics

Next-generation ion mobility mass spectrometry (MS)-based proteomics services available globally to help meet your study needs.

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Gain better insight into the phenotypic response of your therapeutic candidate in organoids and ex vivo patient tissue.

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Certified CRO services with NanoString GeoMx Digital Spatial Profiling.

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De-risk your drug development with early identification of candidate biomarkers and utilize our biomarker discovery services to optimize clinical trial design.

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Rapidly evaluate your molecule’s pharmaceutical and safety properties with our in vivo drug metabolism and pharmacokinetic (DMPK) services to select the most robust drug formulations.

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Explore how the novel HuGEMM™ and HuCELL™ platforms can assess the efficacy of your molecule and accelerate your immuno-oncology drug discovery programs.

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Leverage our suite of structural biology services including, recombinant protein expression and protein crystallography, and target validation services including RNAi.

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Find the most appropriate screen to accelerate your drug development: discover in vivo screens with MuScreen™ and in vitro cell line screening with OmniScreen™.

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Carry out safety pharmacology studies as standalone assessments or embedded within our overall toxicological profiling to assess cardiovascular, metabolic and renal/urinary systems.

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Global CRO in California, USA offering preclinical and translational oncology platforms with high-quality in vivo, in vitro, and ex vivo models.

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On Demand Webinar

Interrogating Syngeneic Models in Large Scale, How to Use Immunoprofiling Data to Improve your Studies

Presenter: Dr. Henry Q Li, Crown Bioscience
Dr. Henry Q Li, Crown Bioscience Inc webinar

Syngeneic models are a standard preclinical platform for evaluating immunotherapies. However, using single, standalone models is less meaningful or productive when testing pharmaceuticals, particularly immunotherapeutics, with diverse mechanisms of action.

To overcome this issue, syngeneic models can be used in a large scale screening platform to assess novel immuno-oncology agents, aiming to rapidly identify model-specific efficacy, resistance, pharmacodynamic effects, and unique combination strategies.

Using a panel of 12 commonly used syngeneic models in this large scale modality, a comprehensive immunoprofiling study has recently been completed to fast-track the in vivo screening of the effects of PD-1, PD-L1, and CTLA-4 blockade. The efficacy and immunophenotyping readouts from this study are helping to address a number of current scientific and technical questions such as:

  • Which models respond to ICI blockade and what is the degree of response?
  • What are the baseline tumor infiltrating immune characteristics of each model at different time points?
  • Which PD parameter is associated with efficacy in different models?
  • Which baseline parameters are most predictive of efficacy?
  • Does time point/tumor size affect reliability of tumor infiltrate analysis?

Watch This Webinar To Discover:

  • How utilizing a large-scale, staggered syngeneic platform can improve efficiency and reproducibility while reducing drug development costs
  • How comprehensive efficacy benchmarking (PD-1/PD-L1/CTLA-4), immunophenotyping, and profiling data can be utilized to address key questions in study design
  • How RNAseq data and FACS/IHC analysis can be used for biomarker discovery to predict response

Watch Now!


About The Presenter:

Dr. Henry Q Li, Crown Bioscience Inc webinarHenry QX Li, PhD leads Crown Bioscience's Global Scientific Research and Innovation Division, focused on accelerating the creation of new, innovative products and services for discovery and translational sciences. Prior to this, Dr. Li successfully led and expanded Crown Bioscience’s patient-derived xenograft (PDX) based Translational Oncology platform (2011-2016), and led the Biomarker and Diagnostic Technologies Division developing novel proprietary translational technologies for precise cancer diagnosis, predictive biomarker discovery, immuno-oncology biomarker detection and quantification, as well as rare cell identification and characterization (2016-2018).

Before joining Crown Bioscience, Dr. Li gained over 20 years of biopharmaceutical, as well as academic R&D, experience in cancer and viral infection, including leadership roles as R&D Director/Senior Director in several US-based biotech companies. Dr. Li currently holds visiting Professor position at Peking University-State Key Laboratory.

Dr. Li earned his PhD in Molecular Biology/Biochemistry from the University of California (Irvine) and completed his postdoctoral training at UCLA School of Medicine. He has published more than 60 manuscripts and edited 3 books in the biopharmaceutical areas. He is also on the editorial board of Current Signal Transduction Therapy.



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