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RECRUITING
NCT07192432
PHASE1/PHASE2

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

Sponsor: Vironexis Biotherapeutics Inc.

View on ClinicalTrials.gov

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.

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

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

27

Start Date

2025-11-18

Completion Date

2033-10

Last Updated

2026-04-01

Healthy Volunteers

No

Interventions

GENETIC

Dose Level 1, VNX-202

Adeno-associated viral vector encoding the CD3/HER2 Bi-Specific T-Cell Engager (AAV.CD3/HER2), Single IV Infusion

GENETIC

Dose Level 2, VNX-202

Adeno-associated viral vector encoding the CD3/HER2 Bi-Specific T-Cell Engager (AAV.CD3/HER2), Single IV Infusion

GENETIC

Dose Level 3, VNX-202

Adeno-associated viral vector encoding the CD3/HER2 Bi-Specific T-Cell Engager (AAV.CD3/HER2), Single IV Infusion

GENETIC

Dose Level 4, VNX-202

Adeno-associated viral vector encoding the CD3/HER2 Bi-Specific T-Cell Engager (AAV.CD3/HER2), Single IV Infusion

Locations (4)

Valkyrie Clinical Trials

Los Angeles, California, United States

SCRI Denver DDU at HealthOne

Denver, Colorado, United States

Thomas Jefferson University, Sidney Kimmel Cancer Center

Philadelphia, Pennsylvania, United States

SCRI Oncology Partners

Nashville, Tennessee, United States