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Accelerated AAV manufacturing with industry-leading performance

OXB delivers fast, flexible, and high-performance AAV manufacturing solutions to support advanced therapy developers worldwide. Our proprietary inAAVateTM platform can deliver GMP AAV in as little as 7 months and consistently achieves high titres and market leading full-to-empty capsid ratios. Alongside platform projects, clients can also tech transfer-in to OXB or work with us on a custom project.

OXB’s AAV track record

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GMP batches successfully released

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Successful regulatory submissions

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months

To GMP release

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17vgs

At 500L scale

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Full capsids

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Analytical assays performed in-house

inAAVate™ platform

Accelerating AAV success from design to GMP

OXB’s inAAVate™ platform provides a robust, standardised foundation to help partners achieve clinical and commercial milestones faster. Our end-to-end platform integrates proprietary technologies across construct design, upstream and downstream processing, analytics, and fill/finish.

Clients can access the Triple Plasmid, or Dual Plasmid System, which together with our proprietary transfection process are responsible for increasing bioreactor vg titre up to 10-fold over typical industry standards.

With the inAAVate™ platform, clients can progress from project initiation to their first GMP batch in as little as 7 months.

Explore the inAAVate™ platform 

Our platform technologies:

Dual plasmid and pHelper:
improved productivity and packaging efficiency.
Dual plasmid and pHelper:
Vector production and Iysis:
optimised and scalable process for improved productivity and packaging.
Vector production and Iysis:
Purification:
robust and scalable AF and AEX process for high% full capsid and control of PTMs for improved potency.
Purification:
Formulation:
broad applicability to multiple serotypes. Demonstrated stability for 18 months at 2-8°C.
Formulation:

Related resources

Novel Dual-Plasmid Transfection System Improves Titer And Product Quality In AAV Manufacturing

27 September, 2024 | AAV

Published in Bioprocess Online, this article explores OXB's novel dual-plasmid system for AAV manufacturing, combining the gene of interest with RepCap in one plasmid and a separate helper plasmid, improving vector genome titers up to 10-fold and increasing full capsid yields to over 90% in the final product.

View PDF >
White Papers

Achieving rAAV Bioreactor Titer of 1E15 vgL With Novel Plasmid Transient Transfection Platform

27 September, 2024 | AAV

In this article, published in Cell and Gene, OXB introduces a high cell density transient transfection platform that achieves recombinant AAV (rAAV) vector genome titers exceeding 1E15 vg/L in bioreactor cultures. This platform incorporates optimized medium additives, plasmid design, and process parameters, enabling successful scale-up to 2,000L bioreactors.

View PDF >
White Papers

AAV: Novel Dual-Plasmid Transfection System

17 September, 2024 | AAV

This brochureintroduces OXB's novel dual plasmid transfection system for AAV development and manufacture.

View PDF >
Brochures

Why choose OXB as your AAV CDMO?

Accelerating AAV Success from design to GMP

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Reach GMP in as little as 7 months

By leveraging the inAAVateTM plug-and-play platform process, the need for excessive process development is eliminated, allowing clients to reach GMP in as little as 7 months.

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Maximise commercial viability with more doses per batch

By continually developing innovative technologies, OXB clients can now achieve titres of 1.5E+17vgs from a 500L bioreactor, with 90% full capsids, delivering cost efficiencies through more doses per batch.

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Effectively manage budgets and milestones

Our flexible delivery and commercial models ensure clients can effectively manage budgets in line with funding milestones and decision points.

Ways to work with us

There are multiple ways in which pharma, biotechs and start-ups work with us, depending on development phase, scale, and individual IP requirements.

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Platform project

For clients that are pre-clinical or early-clinical that wish to reach GMP at an accelerated rate with a proven process.

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Custom solution

For clients that are pre-clinical or early-clinical that require flexibility in the manufacture of their drug candidate.

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Tech-transfer

For clients in phase I, II, or III that need to transfer their manufacture to a CDMO for scale and/or long-term manufacture.

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Frequently asked questions

What is the difference between OXB’s dual plasmid system and triple plasmid system?
What regulatory support does OXB provide for IND and BLA submissions?
Which analytical and QC assays does OXB perform in-house to accelerate GMP batch release?
Which AAV serotypes and capsid variants does OXB have experience with?
How quickly can OXB move from plasmid design to clinical-grade AAV manufacturing?

Platform feasibility in just 6 weeks

For early-stage clients and those that require drug substance for in 
vitro or in vivo studies, we offer a cost-effective platform feasibility project, 
including analytics, in just 6 weeks. Test your gene of interest (GOI) in the inAAVateTM platform.

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