Bintrafusp Alfa in Previously Treated Patients With Recurrent and Metastatic (R/M) Non-keratinizing Nasopharyngeal Carcinoma (NPC)
-
- STATUS
- Recruiting
-
- participants needed
- 37
-
- sponsor
- The University of Hong Kong
Summary
This would be a phase II prospective single
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
Details
Condition |
Metastasis, Brain Metastases, |
---|---|
Age | 18years - 79years |
Treatment | Bintrafusp Alfa |
Clinical Study Identifier | NCT04396886 |
Sponsor | The University of Hong Kong |
Last Modified on | 19 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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