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A Study of VET3-TGI in Patients With Solid Tumors
RECRUITINGPhase 1Sponsored by KaliVir Immunotherapeutics
Actively Recruiting
PhasePhase 1
SponsorKaliVir Immunotherapeutics
Started2024-09-16
Est. completion2027-09-30
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations7 sites
View on ClinicalTrials.gov →
NCT06444815
Summary
VET3-TGI is an oncolytic immunotherapy designed to treat advanced cancers. VET3-TGI has not been given to human patients yet, and the current study is designed to find a safe and effective dose of VET3-TGI when administered by direct injection into tumor(s) (called an intratumoral injection) or when given intravenously (into the vein) both alone and in combination with pembrolizumab in patients with solid tumors (STEALTH-001).
Eligibility
Age: 18 Years+Healthy volunteers accepted
Key Inclusion Criteria: * Have pathologically confirmed, advanced, unresectable, or metastatic solid tumors. Preferred indications include, but are not limited to, breast carcinoma, bladder carcinoma, cervical squamous carcinoma, colorectal carcinoma, esophageal carcinoma, head and neck squamous carcinoma, renal cell carcinoma, ovarian carcinoma, sarcoma, thymoma, and uterine carcinoma. * Failed, intolerant to, or refused potentially curative treatment options, including but not limited to, standard of care molecularly targeted agents, immunotherapy (e.g., anti -pembrolizumab/PDL1 antibodies), and chemotherapy * Measurable disease as per RECIST 1.1 criteria * At least one tumor amenable to safe ITu injections and/or biopsies * ECOG performance status 0 or 1 * Demonstrate adequate organ function * Must be willing to comply with all protocol procedures and adhere to post-treatment care instructions Additional Inclusion criteria exist Key Exclusion Criteria: * Prior systemic therapy washout (dependent upon the therapy) * Requires use of anti-platelet or anti-coagulant therapy that cannot be safely suspended for per protocol biopsies or intra-tumoral injections. * CNS metastases and/or carcinomatous meningitis that have not been completely resected or completely irradiated. * Prior history of myocarditis * Known HIV/AIDS, active HBV or HCV infection. * Receiving high dose immunosuppressive medication or has a significant immunodeficiency (e.g. transplant recipient, etc). Additional Exclusion criteria exist
Conditions12
CancerCervical CancerHead and Neck Squamous Cell CarcinomaKidney CancerLung CancerMelanoma Stage IVMerkel Cell Carcinoma of SkinMesotheliomaMicrosatellite Stable Colorectal CancerNon Small Cell Lung Cancer
Locations7 sites
USC/Norris Comprehensive Cancer Center
Los Angeles, California, 90033
Xiomara Menendez, RNXiomara.Menendez@med.usc.edu
Community Health Network
Indianapolis, Indiana, 46250
Patient Contact317-621-2627
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
PhasePhase 1
SponsorKaliVir Immunotherapeutics
Started2024-09-16
Est. completion2027-09-30
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations7 sites
View on ClinicalTrials.gov →
NCT06444815