Engineered T cell manufacturing service – Accelerate your CGT journey with precision and speed

Our manufacturing workflows for T cell engineering are built on the industry-leading CliniMACS Prodigy® Platform. Integrated and automated, these processes are clinically and commercially proven, delivering robust performance in scalability, consistency, and time-to-market. Leverage our expertise to confidently achieve your cell therapy manufacturing goals.

Expertise you can trust
 

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8 years of experience in T cell engineering and continuously pushing the boundaries

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Viral and non-viral 
engineering expertise*

*Viral: Lentiviral vector, gamma retroviral vector, adenovirus, AAV;
non-viral: CRISPR RNP, ZFN, plasmid DNA, mRNA, transposon/transposase 

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3 late-stage clinical programs

Leverage the leading platform for T cell engineering

  • Clinical and commercialization experience with autologous and allogeneic programs
  • As standard or as custom as you need it
  • Proven platforms to automate your manufacturing and analytics early in your program
Illustration showing the comparison of transducing titers between client plasmids vs. Miltenyi-optimized designs
The CliniMACS Prodigy T Cell Transduction (TCT) Process achieves consistent transduction rates across different runs and constructs.

Excellent transduction efficiency and CAR/TCR frequency

Our automated CliniMACS Prodigy T Cell Transduction Process has been validated in industry and numerous clinical studies. It is designed for standardized and reliable cell manufacturing, delivering excellent transduction efficiencies and target cell frequencies.

Download the brochure on our T cell manufacturing solutions.

Illustration showing the comparison of transducing titers between client plasmids vs. Miltenyi-optimized designs
Excellent CAR T cell expansion rates from fresh and frozen starting materials using the CliniMACS Prodigy Platform.

Optimized T cell expansion rates and final cell count

Our integrated, single platform process boosts your cell expansion rates and maintains favorable T cell phenotypes. Whether you choose fresh or frozen starting materials, different stimulation strategies, or varied production scales, our robust processes bring you closer to your goals.

What you can expect:

  • Consultative and collaborative approach
  • Robust, automated manufacturing process
  • From preclinical to GMP in as little as 9 months*
  • Data packages to enable your CMC section of regulatory filings
  • Flexible clinical manufacturing and scheduling

*Based on data collected through 2024.  Miltenyi Biotec does not guarantee that any specific delivery date(s) will be met.  Individual timelines may vary based on factors such as client’s stage of development and specifications.

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