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Clinical Trials in the USA / NCT07192432
Recruiting Phase 1/2

Gene Therapy for HER-Positive Cancer (SENTRY-HER2)

NCT07192432 · tracked via the Priya Life Science USA tracker
Sponsor
Vironexis Biotherapeutics Inc.
Phase
Phase 1/2
Started
2025-11-18
Last updated
2026-07-28

Condition(s) studied

HER2 Expressing Solid Tumors

Investigational drug(s) / intervention(s)

Dose Level 1, VNX-202Dose Level 2, VNX-202Dose Level 3, VNX-202Dose Level 4, VNX-202

Dose Level 1, VNX-202: Adeno-associated viral vector encoding the CD3/HER2 Bi-Specific T-Cell Engager (AAV.CD3/HER2), Single IV Infusion

Dose Level 2, VNX-202: Adeno-associated viral vector encoding the CD3/HER2 Bi-Specific T-Cell Engager (AAV.CD3/HER2), Single IV Infusion

Dose Level 3, VNX-202: Adeno-associated viral vector encoding the CD3/HER2 Bi-Specific T-Cell Engager (AAV.CD3/HER2), Single IV Infusion

Dose Level 4, VNX-202: Adeno-associated viral vector encoding the CD3/HER2 Bi-Specific T-Cell Engager (AAV.CD3/HER2), Single IV Infusion

Study summary

This is a Phase 1/2, first-in-human, open-label, dose-escalating and expansion trial designed to assess the safety and efficacy of VNX-202 in patients with HER2 positive cancers.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Age: ≥18 years of age * Histologically or cytologically confirmed diagnosis of HER-2 positive solid tumor as defined in the protocol * Part 1: presence of advanced or metastatic disease that has progressed during or following previous treatment * Part 2: Early stage HER-2 positive cancers with high risk for relapse following completion of SOC or after neoadjuvant systemic treatment * AAV specified capsid total antibody ≤1:400 * ECOG performance status of 0 or 1 * Life expectancy ≥3 months * Protocol-specified ranges for renal, liver, cardiac and pulmonary function * Protocol-specified ranges for hematology parameters Exclusion Criteria: * Hepatoxicity (AST or ALT \> 2x upper limit of normal) * Known active CNS or leptomeningeal disease * History of thrombotic microangiopathy or cardiomyopathy, or evidence of sensory neuropathy * Pregnant or nursing (lactating) women * History of other malignancy within 5 years prior to screening as defined in protocol * History of hypersensitivity to corticosteroids or history of corticosteroid-related toxicity Concurrent anti-cancer treatment in another investigational trial

Primary outcome measure(s)

Trial sites (11)

FacilityCityRegionStatus
Valkyrie Clinical Trials Los Angeles California Recruiting
SCRI Denver DDU at HealthOne Denver Colorado Recruiting
Mayo Clinic Jacksonville Florida Recruiting
Mayo Clinic Rochester Minnesota Recruiting
Hackensack Medical Center Hackensack New Jersey Recruiting
Memorial Sloan Kettering Cancer Center New York New York Recruiting
Cleveland Clinic Cleveland Ohio Recruiting
Thomas Jefferson University, Sidney Kimmel Cancer Center Philadelphia Pennsylvania Recruiting
SCRI Oncology Partners Nashville Tennessee Recruiting
UT MD Anderson Cancer Center Houston Texas Recruiting
VCU Massey CTO Phase I Solid Team Richmond Virginia Recruiting

More Vironexis Biotherapeutics Inc. trials in the USA

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07192432 on ClinicalTrials.gov ↗ ← All trials in the USA