Periodic Reporting for period 2 - SPACTORY (SPACTORY, revolutionising pharmaceutical development and manufacturing through microgravity)
Reporting period: 2025-04-01 to 2025-11-30
The SPACTORY project introduces a pioneering solution: the first fully automated, miniaturised drug manufacturing facility designed for operation in space. Leveraging microgravity and advanced lab-on-a-chip technologies, SPACTORY enables the production of high-value biological compounds with superior quality and performance. The facility, weighing only 24 kg and meeting ESA safety standards, is remotely operable and highly modular, making it suitable for current and future space missions, including those on the International Space Station (ISS).
SPACTORY’s overall objective is to validate and demonstrate space-based drug manufacturing with a focus on a target mAb molecule. The project’s pathway to impact includes adapting and qualifying the SPACTORY unit for spaceflight, executing a commercial demonstration mission, and engaging with pharmaceutical stakeholders to establish partnerships for market deployment. The ultimate goal is to open an entirely new frontier in pharmaceutical production, where space is not just a research domain but a platform for scalable, industrial-grade biomanufacturing.
This approach directly supports the European Union’s strategic ambitions in health innovation, technological sovereignty, and space commercialisation. By enabling the production of purer, more stable, and potentially more effective therapeutics, SPACTORY can improve treatment outcomes, reduce healthcare costs, and increase the resilience of medical supply chains. Additionally, the project contributes to the EU’s broader goals in sustainability and competitiveness by laying the foundation for a new industry at the intersection of space and life sciences.
The design of the docking plate and mechanical interfaces to the SpaceRider vehicle has been completed.
The design of the cartridge packaging and the plug-in interfaces to the docking plate has been completed.
The cartridge contents (Fluid Handling System - FHS, electronics, and thermal system) have been successfully adapted to the SPACTORY design specifications.
Electrical Adaptation:
The overall electrical architecture for SPACTORY has been defined.
On-Board Computer (OBC): The board architecture was defined, main components were selected, and an evaluation board was integrated for initial tests. The first version of the OBC board has been designed.
Cartridge Control Board (CCB): The board architecture was defined, main components were selected, and an evaluation board was integrated for initial tests. The first version of the CCB board has been designed and delivered for manufacturing.
Electrical Interfaces: The electrical interfaces between the docking plate and the cartridges have been designed, and the electrical interfaces between the docking plate and SpaceRider have been defined.
Thermal Adaptation:
A comprehensive thermal analysis for SPACTORY under SpaceRider orbiting conditions was performed to define the platform's working profile limitations and establish the basic methods for thermal adaptation.
Scientific progress:
Optimization of the crystallization process to achieve reliable and consistent crystal formation.
Receipt of 1,000 mAb vials to support large-scale experimentation.
Execution of a crystallization experiment launched in August to compare crystal growth results in space versus on Earth
The system enables high-precision crystallisation of monoclonal antibodies (mAbs), which has already led to a breakthrough: successful crystallisation on Earth of a mAb previously considered non-crystallisable. This sets the stage for improved drug purity, stability, and shelf life.
One of SPACTORY’s most impactful innovations is its potential to shift drug delivery from intravenous to subcutaneous injection. This would improve patient comfort, reduce hospitalisation costs, simplify cold-chain logistics, and lower overall healthcare system expenses.
The project is currently collaborating with a major pharmaceutical company to test SPACTORY on existing drugs, aiming to validate real-world applications.
To ensure broader uptake and success, key next steps include:
Further research on the quality and bioactivity of space-grown crystals
Additional in-orbit demonstration missions
Regulatory alignment with EMA/FDA standards
Commercialisation support and funding
Engagement with standardisation and certification bodies
These efforts will help position SPACTORY as a disruptive enabler of next-generation space-enabled biomanufacturing.