Friday, November 22, 2024

Avirmax CMC Received License for cGMP Gene Therapy Vector Production by the California Department

Avirmax CMC Inc., a global leader in recombinant adeno associate virus vector (rAAV) innovation and manufacturing process development, using a recombinant baculovirus Sf9 (rBV-Sf9-AAV) system, has completed its brand-new facility in Hayward, CA (San Francisco Bay Area). The facility has received cGMP license approval by the California Department of Public Health (CDPH)-Food & Drug Branch, for the production of rAAV drug products for use in clinical investigations.

The new 20,000 sq.ft. state-of-the-art manufacturing facility is composed of three functional areas – developmental laboratories, testing laboratories and cGMP production suites consisting of B, C, and D clean room classifications, which are prepared for rAAV Contract Research, Development, Manufacturing Organization (CDMO) service.

The new cGMP facility will support us to deliver high yield and quality vectors efficiently, timely and cost effectively

This facility will produce rAAV using single use bioreactors (SUB) in an animal free, serum free suspension culture system with yields of 1016-17 vector genome (vg) per batch with a production window of about two months. Production scales at 50L, 200L and 1000L, are available to customers depending on their clinical trial size and dose requirements.

Also Read: Innovent Announces First Patient Dosing in Australia in Phase I Study of IBI343 in Patients

The company has a worldwide exclusive license from ViroVek Inc. enabling cGMP production of AAV gene therapeutics using the Bac-to-AAV technology, which utilizes an engineered artificial intron consisting of an insect promoter in both the AAV rep and cap sequences, coupled with a versatile baculovirus expression system. The suspension insect culture system dramatically enhances the stability of recombinant baculoviruses, the infectivity of the AAV vectors, and AAV production yield, capable of reaching as high as 1e+15 vg/L. The Sf9 cell culture provides higher pathogen safety assurance for gene therapy products than those manufactured using human or other mammalian cell culture systems (i.e., HEK293 or HeLa-3 cells) since the Sf9 cell culture hardly supports mammalian virus propagation. The Sf9 manufacturing platform can be operated under a BSL-1 biological safety environment, as used in the production of the recombinant proteins (i.e., monoclonal antibodies) by Chinese hamster ovarian (CHO), baby hamster kidney (BHK) cells.

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