Germantown, MD and Chicago, IL (Dec. 15, 2025) — uBriGene Biosciences, a leading global lentivirus CDMO specializing in Advanced Therapy Medicinal Product (ATMP) GMP development and manufacturing, today announced the official rebranding of its GMP lentiviral vector manufacturing platform to LVV Turbo™, a high-performance system designed to deliver exceptional productivity, superior downstream yields, and a markedly lower cost of LVV manufacturing, enabling faster and more efficient vector development. Alongside this launch, uBriGene is proud to unveil a strategic partnership with Syenex, integrating their proprietary UltraCell™ technology directly into the LVV Turbo™ workflow.
A Next-Generation Manufacturing Platform: LVV Turbo™ + UltraCell™
The LVV Turbo™ + UltraCell™ unifies three disruptive technologies—each addressing long-standing challenges in lentiviral manufacturing:
The LVV Turbo™ + UltraCell™ unifies three disruptive technologies—each addressing long-standing challenges in lentiviral manufacturing:
Together, these innovations substantially reduce COGS for cell therapy developers while maximizing vector potency.
“Our LVV Turbo™ platform resolves the core bottlenecks in LVV manufacturing—boosting productivity, increasing yield, and lowering cost—powered by our disruptive closed downstream system that eliminates sterile filtration and by UltraCell™, which increases T-cell potency and raises transduction titers by up to 5-fold,” said Dr. Xiulian Sun, Chief Technology Officer at uBriGene. “Together, these technologies enable up to 1,500 CAR-T doses from a 20-liter run and alleviates the lentiviral vector supply challenges facing both ex vivo and in vivo CAR-T therapies.”
“We are excited to see UltraCell™ incorporated into uBriGene’s LVV Turbo™ platform, where its 5-fold increase in functional yield for T-cell transduction can have a significant impact on lowering manufacturing costs, particularly for later-stage clinical trials and commercial production where scalability is limiting patient access to curative therapies,” said Jay Rosanelli, Co-Founder and CEO of Syenex.
About uBriGene Biosciences
Founded in 2015, uBriGene Biosciences is a leading Contract Development and Manufacturing Organization for Advanced Therapy Medicinal Products (ATMPs). The company provides integrated CDMO and CRO solutions, encompassing services for cell therapy products, viral vectors, and RNA-related products, with in-house QC testing and regulatory IND filing. Our GMP-validated Maryland facility offers one-stop CDMO services from process development to manufacturing, driving global advancements in ATMPs.
About Syenex
Syenex is an open-science genetic medicines platform company that enables developers to program cells with precision and scale. Leveraging synthetic biology and a global network of contract development and manufacturing organizations (CDMOs), Syenex provides plug-and-play delivery platforms—spanning discovery through GMP manufacturing—so genetic medicine developers can rapidly advance ideas to clinical impact. Founded in 2022, Syenex has assembled a portfolio of cell-specific ex vivo and in vivo delivery platforms and over fifty partnerships with industry leaders across biopharma and academia. Learn more at www.syenex.com.
Contact
uBriGene Biosciences
Mingjuan Liu - Director of Marketing
800-663-2528 / contact@ubrigene.com
Syenex, Inc.
Teresa Nikolich
+1 617 221 5023 - ext 100 / bd@syenex.com