Status:
UNKNOWN
Phase 1 Study Evaluating VT1021 in Patients With Advanced Solid Tumors
Lead Sponsor:
Vigeo Therapeutics, Inc.
Conditions:
Solid Tumor
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
This study is an an open-label Phase I trial of VT1021 in patients with advanced solid tumors. Patients must have recurrent or advanced cancer (i.e., solid tumors) for which standard therapy offers no...
Detailed Description
This is an open-label Phase I study of VT1021 in patients with advanced solid tumors. The study will include a Dose Escalation Phase and a Dose Expansion Phase. Upon determination of the Recommended P...
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
November 28 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2024
Estimated Enrollment :
116 Patients enrolled
Trial Details
Trial ID
NCT03364400
Start Date
November 28 2017
End Date
June 1 2024
Last Update
May 15 2023
Active Locations (12)
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1
Florida Cancer Specialists
Sarasota, Florida, United States, 34232
2
Northwestern Memorial Hospital
Chicago, Illinois, United States, 60611
3
Horizon Oncology Center
Lafayette, Indiana, United States, 47905
4
The Johns Hopkins Hospital
Baltimore, Maryland, United States, 21287