Biotechnology company Rakuten Medical Inc announced on Wednesday that it has signed a biopharmaceutical contract manufacturing agreement with LOTTE Biologics, a South Korea-based company that operates integrated biologics facilities in the United States and South Korea.
This agreement is intended to strengthen Rakuten Medical's production capabilities for its oncology therapy, Alluminox platform-based photoimmunotherapy.
LOTTE Biologics will provide advanced manufacturing services for monoclonal antibody intermediates and their conjugates, supporting Rakuten Medical's global clinical development and future commercialisation.
Rakuten Medical's proprietary photoimmunotherapy technology is designed to selectively target cells in solid tumours, by combining cell-targeting moieties, such as antibodies, with light-activatable agents, enabling focal and selective destruction of solid tumour cells upon light exposure. The therapy is approved in Japan for recurrent head and neck cancer.
A global Phase 3 clinical trial is underway in the United States, Taiwan region and Japan, with plans to start treatment in Ukraine and Poland soon. Rakuten Medical also plans to initiate a Phase 1 clinical trial in Japan for other solid tumours beyond head and neck cancer this year.
FDA accepts rusfertide NDA and grants priority review for polycythemia vera
UAE approves PYRUKYND for treatment of thalassaemia
Sanofi's rilzabrutinib receives orphan drug designation in Japan for IgG4-related disease
Genflow Biosciences receives first EUR336,467 tranche of EUR4m Wallonia grant
Atrium Therapeutics launches as newly independent, publicly traded company
Innovent Biologics' Jaypirca approved in China for new indication
Gemma Biotherapeutics doses first parent in GB221 Phase 1/2 CHARISMA clinical trial
Neurizon Therapeutics doses first participant in NUZ-001 Regimen I HEALEY ALS Platform Trial
Melodia Therapeutics reports award of US patent covering MLD-151
Argo Biopharmaceutical to present BW-20805 Phase II interim data at AAAAI 2026 Annual Meeting
FDA accepts sNDA for MR-141 for the treatment of presbyopia
Bruker launches CellScape XR to advance clinical spatial proteomics
Charles River Laboratories to divest CDMO, Cell Solutions, and European discovery assets