With Binocs as its scheduling engine, Legend Biotech has been able to:
- Protect near‑100% utilization of autologous manufacturing capacity in the critical early years, when demand was far above supply.
- Start commercial manufacturing in the EU within 24 hours of EMA approval, then continue to ramp capacity while maintaining control over complex, multi‑site operations.
- Treat more than 8,000 patients and build towards a network capacity of up to 10,000 patients per year by the end of 2025, while putting in place the processes and tools needed to optimize cost and patient access as demand continues to grow.
“With Binocs, we can track and resolve conflicts by process or operation in real time, maximizing our slot utilization,” James explained.
With Phase 1 complete, Legend Biotech is focusing on:
- Phase 2: SAP integration: Automating data inputs to further reduce manual interventions.
- Phase 3: MES integration: Providing real-time manufacturing data to Binocs for even greater scheduling precision.
- Network-wide rollout: Expanding the system to additional nodes and sites based on best practices established at Raritan.
As James Carr outlined at our 2024 Binocs Community Day, “We’ve realized the importance of digitization in the cell and gene therapy industry. Solutions like Binocs are critical to scaling effectively and delivering for our patients.”
Legend Biotech’s commercial journey with its CARVYKTI therapy–and Binocs’ role in helping them achieve success–was given the spotlight in a recent article from Cell & Gene magazine. Check it out here!
And, if you would like to discuss how Binocs™ can support your own CGT manufacturing or QC operations, we are always happy to share lessons learned from the Legend Biotech partnership and other advanced therapy programs.