MT2021-27 FT538 Recurrent Ovarian, Fallopian Tube, and Primary Peritoneal Cancer

Exclusion Criteria

• •Pregnant or breastfeeding or planning on becoming pregnant in the next 6 months.
• •Currently receiving or likely to require systemic immunosuppressive therapy
• •Active autoimmune disease requiring systemic immunosuppressive therapy.
• •History of severe asthma and currently on chronic systemic medications.
• •Uncontrolled bacterial, fungal or viral infections with progression of clinical symptoms despite therapy.
• •Receipt of any biological therapy, chemotherapy, or radiation therapy (except palliative RT), within 2 weeks prior to the first dose of FT538
• •Live vaccine within 6 weeks prior to start of lympho-conditioning.
• •Known allergy to the following FT538 components: albumin (human) or dimethyl sulfoxide (DMSO).
• •Prior enoblituzumab.
• •Non-malignant CNS disease such as stroke, epilepsy, CNS vasculitis, or neurodegenerative disease or receipt of medications for these conditions in the 2-year period leading up to study enrollment. (Refer to Section 5.1.8 regarding history of brain metastases.)
• •Known history of HIV positivity or active hepatitis C or B - chronic asymptomatic viral hepatitis is allowed.
• •Presence of any medical or social issues that are likely to interfere with study conduct or may cause increased risk to patient.
• •Any medical condition or clinical laboratory abnormality that, per investigator judgement, precludes safe participation in and completion of the study or that could affect compliance with protocol conduct or interpretation of results.