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Merck

Lentiviral Vectors

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Enhancing Quality and De-risking Production for Cell & Gene Therapies

Leveraging our deep experience, knowledge, and expertise from three decades of viral vector development and manufacturing, our VirusExpress® lentivirus platform delivers a high performance, high quality solution to de-risk lentivirus production.

Using our VirusExpress® lentivirus platform, our technical experts can accelerate your path to clinical and commercial GMP manufacturing by providing  streamlined development, scalable manufacturing, and comprehensive analytics.

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Our Track Record

4 x 108 TU/mL

Industry-leading lentivirus titer

< 12

Months to GMP manufacturing

200+ L

Proven, streamlined scalability

300+

Batches of lentiviral vector produced

30

Years of viral vector development and manufacturing

1

One of the first to support commercially approved CAR-Ts


De-risked Lentivirus Production Through Experience

Providing high titer, high yield, and high quality products, our VirusExpress® lentivirus platform has been successfully used in numerous clinical programs. 

Partnering with us you gain an efficient and knowledgeable approach, and confidence in the quality of the clinical and commercial manufacturing of your lentiviral vector.

Our lentivirus platform is fully comprehensive and tailored to meet your timelines:

  • Packaging and transfer plasmids
  • GMP-banked HEK293T cell line
  • Chemically defined cell culture medium
  • Optimized GMP production
  • On-site fill/finish services
  • Comprehensive analytical toolbox
  • Regulatory support services

Lentivirus VirusExpress® Platform Advantages

Our team of development and manufacturing experts have successfully compressed project timelines and seamlessly scaled-up lentivirus cell and gene therapy programs through IND-submission and into clinical trials.

Proven Performance

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  • Successfully used in numerous clinical programs
  • Multiple INDs in process/filed

    Accelerated Timelines

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    • Less than 12 months to GMP manufacturing
    • Save 18 to 20+ months compared to a traditional process timeline

      Cost Savings

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      • Lower operational spend with more productive batches
      • Lower cost per dose

        Comprehensive Analytics

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        • In-house analytical testing
        • Fully qualified external network

          Our Experience is Your Success

          Trusted to advance lentiviral cell and gene therapies for three decades, we have the expertise and knowhow to support your therapeutic from preclinical development through commercialization.

          Contact us to discover how our lentivirus platform can de-risk and optimize your lentiviral vector program to improve performance, quality, reduce costs, and compress development to GMP manufacturing in less than 12 months.



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