ADC Biotechnology announces it has secured investment for the construction of an $11 million bioconjugation facility at its new site in Deeside, North Wales, UK.
The 6,500m facility, scheduled to be operational by December 2018, will support manufacturing in all clinical phases and small-scale commercial production of antibody drug conjugates. It will provide GMP production suites equipped with vessels of 10 up to a few hundred liters for batch sizes from 100 grams up to a kilo. The new integrated facility will enable ADC Bio to complement its long established technical services business that provides small scale R&D through to pre-clinical testing, with three on site laboratories and analytical testing capabilities.
The company’s move into clinical and commercial ADC manufacturing is particularly significant as it already boasts a strong pipeline of customers - thanks to its patented ‘Lock-Release’ technology and the extensive experience of its senior scientists. The aggregation control platform is currently used by over 20 customers, including big pharma, and helps overcome aggregation challenges from the more complex, potent and hydrophobic payloads increasingly coming through discovery and development. The technology immobilizes protein elements, keeping them separated up to the point they are conjugated – ensuring that much cleaner drug products are ultimately released and that the quality and yield of highly aggregated systems are managed in one single step. The technology will also be available for licensing and sublicensing in the future.
“We already have confirmation that many of our existing customers will use the facility for clinical development and we anticipate adding a number of the new targets entering clinical development from customers in the USA and Europe - especially in light of the added value we can provide through Lock-Release. For many of the newer types of payload this could well be the difference between a viable product and not” said Charlie Johnson, CEO of ADC Bio.
The purpose-built, dual stream bioconjugation facility will provide a suite of capabilities ranging from R&D technical services, quality control, QA, warehousing, and process development through to manufacturing – all of which will occupy just 50 percent of the unit’s footprint. Consequently, ADC Bio will have free capacity to upscale quickly from early clinical phases into late phase and commercial manufacturing within the same footprint at the new facility.
Subsequent phases are planned for 2018 onwards and will add further capacity for large scale clinical and commercial, and potentially, dosage form production (fill/finish).
The company’s senior management and scientific team have decades of professional experience of developing ADCs both at ADC Bio and at rival CDMOs. Several of the company's senior management were pivotal to the development and commercialization of Adcetris – the world’s first approved ADC. And, the company is already an integral part of the growing North West pharmaceutical manufacturing hub.