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Gene therapies could revolutionise the treatment of inherited diseases but firms hoping to follow Luxturna to market must remember that, from a manufacturing perspective, the field is still in its infancy.
When the US FDA approved Luxturna for the treatment of the rare, inherited vision loss disease Leber's congenital amaurosis (LCA) in December, it was the gene therapy’s $425,000-a-vial price tag that attracted most attention1.
The focus on price is understandable, particularly given the current debate about US healthcare costs2, but it has meant the technical achievement of bringing Luxturna to market has been somewhat overlooked.
Drug approvals are mainly based on safety and efficacy data, but the FDA also takes manufacturing into consideration.
To win approval, Luxturna developer – Spark Therapeutics – had to prove it makes the drug in a reliable and compliant way, which is an achievement given the complex biological system-based manufacturing steps involved3.
Making gene therapies
A gene therapy is defined as a medicine that treats disease by either introducing genetic material into a cell or modifying the code or expression of an existing gene.
Broadly speaking, there are two types. Those like Luxturna that are delivered using a modified virus and those that are not, like the transposon-based drugs being developed by Poseida Therapeutics.
For virus-based therapies, delivery either takes place outside the body - like Novartis’ Kymriah where a virus inserts genes for a cancer-targeting receptor into harvested immune cells before re-implantation – or inside, like Luxturna.
There are some common phases involved in making a gene therapy - starting with material production; cell line development; manufacture in culture; and harvesting and purification – however, production methods vary per product.
Likewise, there is considerable variation in the manufacturing and processing technologies used to make gene therapies.
Francesca Vitelli, process development head at Lonza’s new gene therapy facility in Houston, Texas4 told us, “The field haven’t reached a consensus on which virus is the best. We work with AAV, lenti, adeno and oncolytic viruses amongst others.
“The methods to make these virus also vary considerably with different cell lines, different helper viruses, different culture methods and different transfection methods for virus production.
"Downstream processing steps are relatively more consolidated, with post-harvest steps comprising a combination of concentration and buffer exchange steps, resin or membrane or monolith chromatography- ideally a capture and a polishing step- and then formulation” she added.
This was echoed by Keith Thompson, CEO of Cell and Gene Therapy Catapult (CGTC) which is a UK-based centre of excellence that fosters innovation in biopharmaceutical manufacturing.
“Traditional pharmaceutical or biologic products have tended towards a common manufacturing process or platform, which can be used to manufacture a variety of different products to treat a broad number of clinical indications.
“The huge variety observed in cell and gene therapy products translates to the plethora of manufacturing processes trialled, with a diverse range of technologies and scales being explored and developed. This is expected to put a significant strain on current GMP manufacturing infrastructure as not all facilities can accommodate the range of processes” Thompson said.
Despite the wide range of manufacturing methods and technologies being employed by the industry, there are some common production bottlenecks according to Vitelli, who cited viral yields as an example.
“Current production steps where the actual virus is assembled or amplified need to be improved to maximize efficient use of cell biomass,” she said, adding that “overall process efficiency throughout all processing steps can be increased for all virus types.”
Vitelli said, “This is similar to the early days in the monoclonal antibody world where 30 years ago, batch quantities were measured in mg/L while now we often see upwards of 5g/L.”
Gene therapy market
Whether Luxturna kick starts the gene therapy market remains to be seen. Issues like immunogenicity and tropism may be more of a problem for drugs not delivered into the eye.
Nevertheless there are positive signs. Vitelli told us, “Gene therapy is in its infancy … but there is a fundamental shift in production philosophy as more personalised medicine understanding spreads.
“Instead of making large quantities of the same molecule in campaign mode, batches will be tailored to more “bespoke molecules” and likely in much smaller scale – even to individual patient scale. The challenge is to be able to scale out to customised smaller quantities rather than scale up, but without negatively impacting COGs.”