Kytopen’s Post

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We are excited to announce the first implementation of our GMP-compliant Flowfect Tx™ cellular engineering platform. GMP Manufacturing of non-viral engineered cells at clinical and commercial levels has now been validated externally by our commercial partner. "We are committed to leading the way in helping the industry accelerate development and address the challenges in the manufacture of advanced cell therapies. This is the first of many applications in our pipeline and we are eager to partner with therapeutic companies worldwide.” – CEO, Dr. Michael Chiu Read the full press release: https://lnkd.in/gac4E3EB #celltherapy #regenerativemedicine #cancer #cancerresearch #geneediting

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Michael Chiu

CEO at Kytopen, Inc.

3mo

This is a huge milestone for Kytopen, and demonstrates that the Flowfect platform is ready to support our customer’s clinical and commercial programs. The speed of this project and performance with their process confirms that Kytopen is the best option for speed to patient at any scale. This was not an individual effort; great work and thanks to the entire Kytopen team!

Ben Lefroy

Lead Mechanical Engineer | Scientific Instrument Design | Med-Tech R&D to Manufacturing

2mo

This is such good news - well done Kytopen team for getting this far, and I’m excited to hear what else you achieve!

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Carl Schoellhammer

Partner - Biopharma and Advanced Therapies, DeciBio Consulting; Investor, BioTools Fund; Founder / Director, Suono Bio

3mo

Congrats, Michael Chiu and team

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Karen Weisinger

VP, Science & Technology | Cell therapies | iPSC | Process Development | CMC | Scale-up technologies | R&D | Cross functional team | Leadership | Cross discipline communication | GMP device development |

3mo

Amazing strides! Congratulations to the Kytopen team.

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Sounds great, Mike! Congrats!

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