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

RecruitingPhase 1/2

A Phase 1/2, First-in-Human Study of VNX-202 Gene Therapy in Patients With HER2-Positive Cancer

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
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

About the study

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.

What is being tested

Sponsor: Vironexis Biotherapeutics Inc. · Participants: 27 · Started: Nov 18, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07192432

Locations in the U.S.

CaliforniaValkyrie Clinical Trials, Los Angeles
ColoradoSCRI Denver DDU at HealthOne, Denver
FloridaMayo Clinic, Jacksonville
MinnesotaMayo Clinic, Rochester
New JerseyHackensack Medical Center, Hackensack
New YorkMemorial Sloan Kettering Cancer Center, New York
OhioCleveland Clinic, Cleveland
PennsylvaniaThomas Jefferson University, Sidney Kimmel Cancer Center, Philadelphia
TennesseeSCRI Oncology Partners, Nashville
TexasUT MD Anderson Cancer Center, Houston
VirginiaVCU Massey CTO Phase I Solid Team, Richmond

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.