Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Adaptimmune
Age
18–75
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Age ≥18 and \<75 years
Diagnosis of head and neck squamous cell carcinoma with metastatic or unresectable, recurrent disease. confirmed by histology cytology.
Checkpoint inhibitor naïve and indicated for pembrolizumab or currently receiving pembrolizumab (monotherapy). May have received prior platinum containing chemotherapy regimen or checkpoint inhibitor therapy.
Subjects that have already received pembrolizumab (alone or in combination) and are progressing or have completed immune checkpoint inhibitor therapy for recurrent/metastatic disease, may still be enrolled and will skip Part A of the study.
These subjects will enroll into Part B when manufactured T cells are available.
Measurable disease according to RECIST v1.1.
HLA-A\*02 positive by central laboratory.
Tumor shows MAGE-A4 expression confirmed by central laboratory.
ECOG Performance Status of 0 or 1.
Left ventricular ejection fraction (LVEF) ≥50%.
You may not be if
Positive for any HLA-A\*02 allele other than: one of the inclusion alleles, HLA- A\*02:07P or HLA-A\*02 null alleles
History of allergic reactions attributed to compounds of similar chemical or biologic composition to fludarabine, cyclophosphamide or other agents used in the study or history of severe hypersensitivity to another monoclonal antibody.
History of autoimmune or immune mediated disease
Leptomeningeal disease, carcinomatous meningitis or CNS metastases.
Other prior malignancy that is not considered by the Investigator to be in complete remission
Clinically significant cardiovascular disease
Uncontrolled intercurrent illness
Active infection with human immunodeficiency virus, hepatitis B virus, hepatitis C virus, or human T cell leukemia virus
