Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Fate Therapeutics
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Locally advanced or metastatic solid tumor malignancies that have relapsed or progressed after at least one line of therapy and where the following anti-PD-L1 are approved: avelumab, atezolizumab or durvalumab
Capable of giving signed informed consent
Aged ≥ 18 years old
Willingness to comply with study procedures and duration
Measurable disease per iRECIST
Contraceptive use for women and men as defined in the protocol
You may not be if
Pregnant or breast-feeding women
ECOG performance status ≥ 2
Evidence of insufficient organ function
Clinically significant cardiovascular disease
Receipt of therapy within 2 weeks prior to Day 1 or five half-lives, whichever is shorter or any investigational therapy within 28 days prior to Day 1
Known active central nervous system (CNS) involvement by malignancy
Non-malignant CNS disease such as stroke, epilepsy, CNS vasculitis or neurodegenerative disease or receipt of medications for these conditions
Currently receiving or likely to require immunosuppressive therapy
Known active infections with Hepatitis B, Hepatitis C or HIV
Live vaccine within 6 weeks prior to start of lympho-conditioning
Known allergy to albumin (human) or DMSO
Clareo Health | FT516 in Combination With Monoclonal Antibodies in Advanced Solid Tumors
