Targeted CAR-T Cell Therapy (IVS-3001) for the Treatment of Previously Treated Locally Advanced Unresectable or Metastatic HLA-G Positive Solid Tumors

Inclusion Criteria

• Each subject (or their legally acceptable representative) must sign and date an informed consent form approved by the institutional review board, as appropriate, indicating that he/she understands the purpose of, and procedures required for the study and are willing to comply. Consent is to be obtained prior to the performance of any study-specific procedures or tests that are not part of the standard of care for the subject’s disease.
• Age >= 18 years old
• Histologically or pathologically confirmed diagnosis of a locally advanced unresectable or metastatic HLA-G+ select solid tumor malignancy who failed or intolerant to standard of care therapies known to confer clinical benefit per treating physician * For Phase 2a, eligible subjects will be enrolled into indication-specific cohorts: ** Cohort 1: HLA-G+ clear cell renal cell carcinoma who failed or intolerant to checkpoint inhibitor (CPI) and tyrosine kinase inhibitor (TKI) ** Cohort 2: Epithelial ovarian carcinoma who failed or intolerant to platinum-based therapy, and should have failed or intolerant for PARP inhibitor if BRCA 1/2 mutated ** Cohort 3: Other HLA-G+ tumors (biomarker driven) who failed or intolerant to at least one prior line of therapy and for whom at discretion of treating physician there is no standard therapy to confer a clinical benefit
• HLA-G expression on tumor cells (>10% expression will be determined as HLA-G positivity) as determined by immunohistochemistry (IHC) analysis on tumor biopsies using the 4H84 antibody
• Measurable disease (at least one target lesion) per Response Evaluation Criteria in Solid Tumors (RECIST) version (v) 1.1. Measurable disease per RECIST v1.1 is not required at the time of apheresis but required before IVS-3001 CAR-T infusion. In the rare event when the tumor is still not measurable per RECIST v1.1, infusion date will be postponed
• Life expectancy > 12 weeks
• Availability of a pre-treatment tumor archived tissue specimen to test for HLA-G expression. In case an archival tissue is not available, patients should be willing to consent for pretreatment biopsy to screen for HLA-G expression
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• Subjects must have adequate venous access for apheresis or agree to use of a central line for apheresis collection
• Left ventricular ejection fraction (LVEF) at rest must be > 45%
• Absolute lymphocyte count >= 300/uL
• Absolute neutrophil count >= 1,000/uL
• Platelets >= 75,000/uL
• Hemoglobin >= 8.0 g/dL
• Total bilirubin =< 1.5 x upper limit of normal (ULN), or =< 3x ULN if due to Gilbert’s disease
• Serum aspartate aminotransferase and alanine aminotransferase =< 3 x ULN or =< 5 x ULN if liver metastases are present
• Creatinine =< 1.5 x ULN or estimated glomerular filtration rate (eGFR) >= 45 ml/min or creatinine clearance (using Cockcroft-Gault formula) ≥ 45 ml/min
• From the time of screening/study treatment informed consent form (ICF) signature, a female subject must be either: * Not of childbearing potential defined as: ** Postmenopausal (> 45 years of age with amenorrhea >=12 months) ** Permanently sterilized ** Otherwise, incapable of pregnancy * Of childbearing potential and agrees to use 2 highly effective methods of birth control (Effectiveness of Contraception Methods, Centers for Disease Control [CDC] 2018) before lymphodepletion and for at least 12 months after lymphodepletion
• From the time of screening/study treatment ICF signature, male subjects with female partners of childbearing potential must agree to use 2 highly effective methods of birth control (Effectiveness of Contraception Methods, CDC 2018) for at least 12 months after the last dose of IVS-3001
• Non-English speaking subjects may be enrolled

Exclusion Criteria

• Systemic cancer treatments should be stopped at least 2 weeks prior to apheresis
• Note: Bridging therapies (including herbal therapies and immunotherapies) are allowed up to 2 weeks before start of lymphodepletion (5 weeks for nitrosoureas or mitomycin) or 5 half-lives, whichever is shorter and must be reported in the Case Report Form (CRF). Palliative radiotherapy is permitted but must be completed at least 2 weeks prior to IVS-3001 infusion. Symptomatic, untreated, or actively progressing central nervous system metastases (subjects with prior brain metastases treated at least 2 weeks prior to the planned IVS-3001 infusion who are clinically stable and do not require chronic corticosteroid treatment are allowed
• Symptomatic, untreated, or actively progressing central nervous system metastases (subjects with prior brain metastases treated at least 2 weeks prior to the planned IVS-3001 infusion who are clinically stable and do not require chronic corticosteroid treatment are allowed
• Primary malignant central nervous system (CNS) tumors
• History or presence of clinically relevant uncontrolled CNS disorder such as uncontrolled seizures, stroke and severe brain injuries, dementia, Parkinson’s disease, cerebellar disease, organic brain syndrome, psychosis, or leptomeningeal disease
• Ongoing toxicities related to prior anticancer therapy that have not resolved to grade =< 1 (other than alopecia) * Note: Current unresolved grade >= 2 non-hematologic toxicity may be allowed after discussing with the study chair/Co-chair
• Receiving investigational anti cancer treatment within 4 weeks before cell infusion
• Active autoimmune disease, chronic infection or any disease requiring systemic immunosuppressive therapy (e.g., calcineurin inhibitors, methotrexate, immunosuppressive antibodies such as anti-IL-6 or anti-IL-6-receptor)
• Prior exposure to HLA-G targeted genetically modified cell therapy
• Prior exposure to genetically modified cellular therapies using lentivirus * Note: CAR T-cell products not using lentivirus and not targeting HLA-G are allowed. A washout time of, at least 3 months from cell infusion is then required
• Impaired cardiac function or clinically significant cardiac disease, including any of the following: * Symptomatic congestive heart failure requiring treatment * Clinically significant cardiac arrhythmia * Uncontrolled hypertension * Acute myocardial infarction or unstable angina pectoris within 6 months prior to signing main consent * Fridericia's correction formula (QTcF) > 480 msec; or, marked limitation of physical activity due to symptoms, or unable to carry on any physical activity without discomfort (New York Heart Association Functional Class III-IV)
• Major surgical procedure, other than for diagnosis, within 4 weeks prior to signing main consent, or anticipation of the need for a major surgical procedure during the study
• Received a vaccine containing live virus within 6 weeks prior the lymphodepletion
• Treatment with systemic chronic steroid therapy (prednisone >= 10 mg/day or equivalent) or any other immunosuppressive therapy (including, but not limited to, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor [anti-TNF] agents) within 7 days or 7 half- lives of the prescribed therapy, whichever is shorter, prior to the planned apheresis date. Note: * The use of inhaled corticosteroids and mineralocorticoids (e.g., fludrocortisone) for patients with orthostatic hypotension or adrenocortical insufficiency is allowed * Physiological doses of corticosteroids such as for adrenocortical insufficiency or other indications are allowed
• Uncontrolled intercurrent illness including but not limited to poorly controlled hypertension or diabetes, or any medical condition determined by the investigator to be a risk for enrolling in the protocol
• Untreated or active infection at the time of initial screening, within 72 hours before lymphodepletion or at the time of leukapheresis. Prior oral or IV antibiotics antifungals or antiviral medications must be completed at least 1 week prior to IVS-3001 infusion except for use of prophylactic antimicrobial agents
• Active hepatitis B, active hepatitis C, or any human immunodeficiency virus (HIV) infection at the time of screening: * Active hepatitis B virus (HBV) infection (chronic or acute), defined as having a positive hepatitis B surface antigen (HBsAg) test during screening. Subjects with a past or resolved HBV infection, defined as having a negative HBsAg test and a positive total hepatitis B core antibody (HBc Ab) test at screening are eligible for the study if HBV deoxyribonucleic acid (DNA) test is negative. If a subject has a negative HBsAg test and a positive total HBc Ab test at screening, an HBV DNA test should be performed HBV viral load must be less than 100 UI/mL evaluated by polymerase chain reaction (PCR) * Active hepatitis C virus (HCV) infection, defined as having a positive HCV antibody test followed by a positive HCV ribonucleic acid (RNA) test during screening. The HCV RNA test will be performed only for subjects who have a positive HCV test. If patient is known to have HCV infection, the viral load must be less than 100 UI/mL evaluated by PCR
• History of grade >= 2 bleeding within 4 weeks
• Subjects with symptomatic intrinsic lung disease
• Subject is a woman of child-bearing potential and is pregnant (positive serum beta-human choriogonadotropin test at baseline), planning to become pregnant within 12 months after lymphodepletion, or is breastfeeding
• Subject is a man who plans to donate sperm or father a child within 12 months after lymphodepletion
• History of second primary malignant disease with the following exceptions: * Malignancies that were treated and have not recurred within 2 years prior to screening * Completely resected basal cell or squamous cell skin cancers * Any malignancy considered to be indolent, not requiring therapy and with low metastatic potential