Clinical Research Directory

Inclusion Criteria: 1. Able to understand and voluntarily sign an informed consent form (ICF). 2. Adult aged ≥ 18 years at the time of informed consent (or other age required by local regulations). 3. Confirmed diagnosis of any of the following solid tumor: 1. Head and neck squamous cell carcinoma, excluding nasopharyngeal carcinoma; 2. Hepatocellular carcinoma; 3. Lung squamous cell carcinoma; 4. Synovial sarcoma; 5. Triple-negative breast cancer; 6. Esophageal squamous cell carcinoma; 7. Cervical cancer; 8. Ovarian cancer 4. Patient who received standard curative or palliative therapy including but not limited to any targeted therapy based on mutation status for their cancer, or patient with advanced solid tumors for which there is no accepted therapy, standard therapies are no longer effective, or the patient refuses additional standard therapy. 5. Eastern Cooperative Oncology Group (ECOG) Performance Status ≤1. 6. Body weight ≥ 50 Kg. 7. Life expectancy of ≥ 6 months. 8. Patient who agrees to provide the tumor sample for NY-ESO-1 IHC staining, from either fresh or archival tissue Exclusion Criteria: 1. Known primary immunodeficiency (such as Severe Combined Immunodeficiency Disease or AIDS). 2. Uncontrolled intercurrent illness which is not suitable for enrollment at the discretion of the investigator, including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, unstable cardiac arrhythmia, psychiatric illness, or social situations that would limit compliance with study requirements. 3. Currently confirmed diagnosis of at least 2 active cancers; patient who was cured of the other cancer \[disease free period \> 6 months\] and currently has only one research targeted tumor can be enrolled. 4. Untreated or symptomatic brain metastasis. 5. History of organ transplantation or allogeneic stem cell transplantation. 6. Other conditions (e.g. previous use of any cell therapy) which are not suitable for enrollment at the discretion of the investigator.