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Clinical Trial Summary

This would be a phase II prospective single arm mono-institutional study conducted in Queen Mary Hospital (Hong Kong) assessing the efficacy and safety of bintrafusp alfa in previously treated patients with recurrent and metastatic (R/M) non-keratinizing nasopharyngeal carcinoma (NPC)


Clinical Trial Description

All the patients must be registered with the Investigator(s) prior to initiation of treatment. The registration desk will confirm all eligibility criteria and obtain essential information (including patient number).

Patients shall receive Bintrafusp alfa treatment through intravenous therapy every two weeks up until disease progression, unacceptable toxicity or for a maximum of 2 years. Survival Follow-up till 5 years will also be performed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04284332
Study type Interventional
Source The University of Hong Kong
Contact
Status Not yet recruiting
Phase Phase 2
Start date February 28, 2020
Completion date January 30, 2023

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