Phase 1 Study Evaluating VT1021 in Patients With Advanced Solid Tumors

Inclusion Criteria:

Dose Escalation Phase:

Patients must be refractory to, or intolerant of, existing therapies known to provide clinical benefit for their condition (i.e., cancer diagnosis)

Dose Expansion Phase:

Ovarian:

Patients with confirmed diagnosis of unresectable epithelial ovarian, fallopian tube, or primary peritoneal cancer must have received ≤ 3 prior lines of therapy in a platinum resistant setting. BRCA mutant patients are excluded unless they have failed previous line with a PARP inhibitor

Pancreatic:

Patients with confirmed diagnosis of pancreatic cancer must have received ≤2 prior lines of therapy

Triple Negative Breast Cancer:

Patients with confirmed diagnosis of metastatic TNBC must have received ≤ 3 prior lines of therapy for metastatic disease

Glioblastoma:

Patients with confirmed relapsed or refractory glioblastoma must have received ≤2 prior lines of systemic therapy

CD36-high basket cohort:

Patients with solid tumor cancers that have high expression of CD36 by immunohistochemistry. Patients must have received ≤ 3 prior lines of therapy for metastatic disease

Patient has evaluable disease by RECIST v1.1
Patient has a performance status (PS) of 0-2 on the Eastern Cooperative Oncology Group (ECOG) scale
Patient is at least 21 days (12 weeks for glioblastoma patients) removed from therapeutic radiation or chemotherapy prior to the first scheduled day of dosing with VT1021
Patient has adequate organ function
Patient agrees to use acceptable methods of contraception during the study and 60 days after the last dose of VT1021

Exclusion Criteria:

Diagnosis of another malignancy within the past 2 years (excluding a history of carcinoma in situ of the cervix, superficial non-melanoma skin cancer, superficial bladder cancer, or endometrial cancer that has been adequately treated, or stage 1 prostate cancer that does not require treatment)
History of a major surgical procedure or a significant traumatic injury within 14 days prior to commencing treatment, or the anticipation of the need for a major surgical procedure during the course of the study
Treatment with investigational therapy(ies) within 5 half-lives of the investigational therapy prior to the first scheduled day of dosing with VT1021, or 4 weeks if the half-life of the investigational agent is not known
Concurrent serious (as determined by the Principal Investigator) medical conditions, including, but not limited to, New York Heart Association (NYHA) class III or IV congestive heart failure, history of congenital prolonged QT syndrome, uncontrolled infection, active hepatitis B, hepatitis C or HIV, or other significant co-morbid conditions that, in the opinion of the Investigator, would impair study participation or cooperation
Pregnancy or lactation
Evidence of symptomatic brain metastases. Patients with treated (surgically excised or irradiated) and stable brain metastases are eligible, assuming the patient has adequately recovered from treatment
Other concurrent chemotherapy, immunotherapy, radiotherapy or investigational therapy
Requirement to palliative radiotherapy to lesions that are defined as target lesions by RECIST criteria at the time of study entry