Nasopharyngeal Cancer Clinical Trial
Official title:
A Cancer Research UK (CR-UK) Phase Ib Trial to Determine the Safety, Tolerability and Immunogenicity of Extended Schedule Vaccination With MVA-EBNA1/LMP2 in Patients With Epstein Barr Virus Positive (EBV+) Nasopharyngeal Carcinoma (NPC).
This clinical study is looking at a vaccine called MVA-EBNA1/LMP2. This is a new vaccine that
has already been studied in small number of cancer patients.
The vaccine is designed to boost a patient's immunity against a common virus. The virus is
called Epstein Barr virus or EBV. EBV is sometimes found inside cancer cells and is commonly
found in nasopharyngeal cancer cells.
The main aims of the clinical study are to find out more about how the immune system responds
to the vaccine, more about the potential side effects of the vaccine and the effects of
giving an additional booster vaccination on the immune system.
Approximately 18 patients with EBV positive nasopharyngeal cancer (NPC) will be recruited to
the trial. Patients will receive up to four vaccinations with the MVA-EBNA1/LMP2 vaccine. The
first three vaccines will be given at 3 weekly intervals, followed by a fourth vaccine 12
weeks later. The vaccine will be given by intradermal injection with the dose divided across
multiple injection sites on the arm, or on the thigh.
Patients will participate in the study for approximately 12 months from first vaccination and
attend hospital approximately 11 times during this period. Standard safety assessments will
be performed throughout the trial and at each clinic visit patients will be asked to provide
research blood samples. These samples will be used to monitor the effects of the vaccine on
the patient's immune system.
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