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Bispecific & Multispecific Antibodies

Utilizing leading BsAb engineering and discovery platforms to enable efficient CMC development and manufacturing

Starting with our bispecific antibody (bsAb) and multispecific antibody (msAb) engineering, generation and screening platforms, WuXi Biologics seamlessly integrates discovery, CMC development, and GMP manufacturing to offer our global clients a streamlined solution for accelerating these next-generation biologics from concept to commercialization. With state-of-the-art facilities and a proven track record of success, our expert CRDMO teams deliver innovative solutions for bispecific and multispecific antibody developers. Experience unparalleled efficiency, reliability, and quality with WuXi Biologics as your trusted single-source partner to advance your bsAb and msAb to the clinic and beyond.

Expand the menus below to see the full range of our one-stop target to market services for bsAb. and msAbs.

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  • Research Material Generation
  • Target Evaluation and Identificatoin
  • BsAb / MsAb Discovery (Antibody Generation, Engineering & Screening)
    • WuXiBodyTM Bispecific Antibody Platform
    • SDARBodyTM Bispecific/Multispecific VHH-Based Platform
    • SkyBodyTM Bispecific/Multispecific scFV-Based Platform
    • Omniflic® Common Light Chain Transgenic Platform
    • General BsAb Technology Platform
  • Developability Assessment
  • Lead Optimization
  • In vitro Characterization
  • In vivo Characterization
  • R&D Scale Protein Generation
  • Cell Line Development
  • GMP Cell Banking and Characterization
  • Upstream Cell Culture Development
  • Downstream Purification Development
  • Analytical Development
  • Formulation Development
  • Drug Product Development
  • Pilot Manufacturing
  • Viral Clearance Validation
  • GMP Manufacturing (Drug Substance)
  • GMP Manufacturing / Fill (Drug Product)
  • QC Release and Stability Testing
  • IND Filing / Regulatory Support
  • Technical Transfer
  • Cell Line Development / Optimizatoin
  • GMP Cell Banking and Characterization
  • Upstream Cell Culture Development/Optimization
  • Downstream Purification Development/Optimization
  • Process Characterizatoin and Validation
  • Analytical Development and Validatoin
  • Final Formulation Optimizatoin and Lock
  • Drug Product Development and Process Lock
  • Performance Process Qualification (PPQ) Runs
  • Viral Clearance Validation
  • GMP Manufacturing (Drug Substance)
  • GMP Manufacturing / Fill (Drug Product)
  • QC Release and Stability Testing
  • BLA Submission / Regulatory Support

Our industry experts and highly trained scientific teams have successfully executed over 450 integrated mAb client projects, spanning from early discovery to market launch, within our global facilities. With this extensive experience and unmatched knowledge base, we ensure a seamless and effective project execution from the start, promoting right-first-time outcomes.

For more information

See these additional resources and search our various peer-reviewed scientific articles to learn more about our vast bsAb / msAb services and capabilities:

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Let’s discuss your project needs.
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