Leo Pharma Acquires EU Rights to Loqtorzi, Boosting Marketing Efforts for PD-1 Inhibitor
EU Rights Acquisition:
Leo Pharma has secured the rights to promote and sell Loqtorzi (toripalimab), a PD-1 inhibitor, in the European Union from Shanghai Junshi Biosciences24.
Indications:
Loqtorzi is indicated for the first-line treatment of nasopharyngeal carcinoma (NPC) in combination with cisplatin and gemcitabine, and as a monotherapy for recurrent, unresectable, or metastatic NPC with disease progression on or after platinum-containing chemotherapy13.
Clinical Efficacy:
Loqtorzi has demonstrated significant improvements in progression-free survival (PFS) and overall survival (OS) in clinical trials. It reduced the risk of disease progression or death by 48% and the risk of death by 37% compared to chemotherapy alone13.
Mechanism of Action:
Loqtorzi is an anti-PD-1 humanized IgG4 monoclonal antibody that blocks the interaction between PD-1 and its ligands, enhancing the immune response against tumor cells13.
Future Developments:
Loqtorzi is also being explored for other indications, including advanced hepatocellular carcinoma (HCC), where it has shown promising results in a Phase III study5.
Sources:
1. https://www.clinicaltrialsarena.com/projects/loqtorzi-treatment-nasopharyngeal-carcinoma-us/
2. https://www.fiercepharma.com/pharma
3. https://investors.coherus.com/news-releases/news-release-details/coherus-and-junshi-biosciences-announce-fda-approval-loqtorzitm
4. https://www.raps.org/news-and-articles/news-articles/2025/1/recon-j-j-s-spravato-gets-fda-approval-for-depress
5. https://www.biospace.com/coherus-junshi-s-pd-1-blocker-loqtorzi-aces-phase-iii-liver-cancer-trial