CDMO SERVICES

A dedicated solution provider of cellular therapy products

CAR-T
CDMO Services for Plasmids-IIT grade/non-clinical phase

Manufacturing of plasmids, a critical step of manufacturing TCR-T cellular therapy products, involves a series of complicated processes of manufacturing, purification, and analysis. As essential tools for genetic engineering, bacterial plasmids can not only be used as final products for gene and cellular therapy, but also as intermediate vectors for the manufacturing of gene and cell therapy products, and are inevitably used in manufacturing steps for most gene and cellular therapy products. With the emergence of the cellular therapy industry, the market demands for plasmids are also increasing with each passing year. Hillgene is specialized in the provision of integrated CDMO solutions for cellular therapy products, has established a GMP manufacturing platform for nucleic acid products, and therefore, can provide high-quality CDMO services for plasmids to clients with various demands.

Services 

CDMO Services for Plasmids
TypesServices
IIT grade1Independently developed four-plasmid system

● Third generation four-plasmid system

● Kanamycin-resistance gene

● No patent license required

● Seamless connection to IND submission

● GMP-like workshop

● GMP-like quality management system

● Authentic and traceable documentation

2Creation of bacteria bank (GMP-like)

● Tailorable number and specification of bacteria banks to be created

3Plasmid Manufacturing and Testing (GMP-like)

● Tailorable production output and specification

*Note: We offer relatively flexible and customized changes to above services, including but not limited to above services.



Advantages

Advantages of our plasmid system:

• An independently developed four-plasmid system with kanamycin-resistance gene 

• A system with the capability of sustained optimization 

• Plasmid sequences are traceable, compliant with requirements, and efficient  

• Extensive experience in successful IND submissions 

• TCR-T cell samples for clinical use are currently manufacturing and in use 

• 2-5 folds higher titers after using our plasmid system from the comparison in several projects

Advantages of our plasmid manufacturing:

• Free of antibiotics throughout the manufacturing process 

• Plasmid production and bank creation in separate workshops 

• Complete isolation between non-sterile and sterile areas 

• Dispensing final products using an isolator  

• Completed CTD dossiers for packaging plasmid (for lentiviral vector), reducing the submission preparation time by 3-4 months, with INDs of a few products granted preliminary approval and currently in phase I of clinical study



Manufacturing process


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Quality control

Test ItemTest Method
AppearanceVisual inspection
IdentificationIdentification 1Restriction mapping
Identification 2Sanger sequencing
TestpHMethod 0631 of ChP 2020
PurityHigh performance liquid chromatography (HPLC)
Residual E.coli host cell proteinELISA
Residual E.coli DNAq-PCR
Residual E.coli RNAq-PCR

Residual antibiotics

ELISA
EndotoxinMethod 1143 of ChP 2020
SterilityMethod 1101 of ChP 2020
Concentration determinationDNA concentrationMethod 0401 of ChP 2020

*Note: Hillgene established QC methods corresponding to different technology platforms, with QC methods including but not limited to above items.



Project Timeline

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Project Management Plan

Hillgene Project Management Team, consisting of chief scientists, project managers, Project QA and GMP experts, will make efforts to ensure the smooth and sound operation of each and every GMP project.


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