Clinical Trials

Inclusion Criteria:

• Age ≥ 18 years.

• Histologically confirmed solid malignancy or healthy individuals.

• Willing to provide mandatory research blood draw or apheresis per protocol (see Section 17.0).

• Provide written informed consent.

• Negative pregnancy test done ≤7 days prior to pre-registration for persons of childbearing potential only.

NOTE: A serum pregnancy test will be required if the urine test is positive or cannot be confirmed as negative.

• The following laboratory values obtained ≤ 28 days prior to registration.

  • Hemoglobin ≥910.0 g/dl

  • Absolute neutrophil count (ANC) ≥1500/mm3

  • Platelet count ≥100,000/mm3

Exclusion Criteria:

• Any of the following prior therapies:

  • IV antibiotic ≤2 weeks prior to apheresis

  • Major Surgery ≤4 weeks prior to registration

  • Received a live vaccine ≤30 days prior to registration

• Active hematologic malignancies ≤ 3 years prior to registration.

• Immunocompromised patients and patients known to be HIV positive and currently receiving antiretroviral therapy.

• History of active tuberculosis (TB), human immunodeficiency virus (HIV), active hepatitis B (e.g., HBsAg reactive), and/or active hepatitis C infection (e.g., HCV RNA qualitative is detected).

• Known history of active autoimmune disease that has required systemic treatment in the ≤14 days (i.e., with the use of disease-modifying agents, corticosteroids >10 mg daily prednisone equivalent, or other immunosuppressive drugs) prior to pre-registration.

NOTE: Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment. Patients with vitiligo, Graves’ disease, or psoriasis not requiring systemic treatment within the past 30 days are not excluded. Patients with Celiac disease controlled with diet modification are not excluded.

• Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 5/14/2025. Questions regarding updates should be directed to the study team contact.