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EMA Product

Loqtorzi

Product approved by European Medicines Agency (EU)

Basic Information

Loqtorzi

Regulatory Information

EMEA/H/C/006120

Authorised

September 19, 2024

July 25, 2024

1

April 8, 2025

Company Information

Ireland

Ground Floor Two Dockland Central Guild Street I.F.S.C. Dublin 1 Co. Dublin D01 K2C5

TOPALLIANCE BIOSCIENCES EUROPE LIMITED

Drug Classification

Additional Monitoring

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Loqtorzi, in combination with cisplatin and gemcitabine, is indicated for the first-line treatment of adult patients with recurrent, not amenable to surgery or radiotherapy, or metastatic nasopharyngeal carcinoma. Loqtorzi, in combination with cisplatin and paclitaxel, is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent, or metastatic oesophageal squamous cell carcinoma.

Overview Summary

Loqtorzi is a cancer medicine used in adults to treat: - nasopharyngeal cancer (cancer of the nasopharynx, where the throat and nose connect) that is recurrent (has come back) and cannot be treated with surgery or radiotherapy or is metastatic (has spread to other parts of the body). It is used together with cisplatin and gemcitabine, other cancer medicines (also known as chemotherapy); - oesophageal squamous cell cancer, a type of cancer affecting the oesophagus (the passage from the mouth to the stomach). It is used when the cancer is advanced and cannot be removed by surgery or if it is recurrent or metastatic. It is used together with the chemotherapy medicines cisplatin and paclitaxel. Loqtorzi contains the active substance toripalimab.

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