OncoMatch/Clinical Trials/NCT03740256
Binary Oncolytic Adenovirus in Combination With HER2-Specific Autologous CAR VST, Advanced HER2 Positive Solid Tumors
Is NCT03740256 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies CAdVEC for bladder cancer.
Treatment: CAdVEC — This study is a first in human Phase 1 study that involves patients with a type of cancer called HER2 (Human Epidermal Growth Factor Receptor 2) positive cancer. This study asks patients to volunteer to take part in a research study investigating the safety and efficacy of using special immune cells called HER2 chimeric antigen receptor specific cytotoxic T lymphocytes (HER2 specific CAR T cells), in combination with intra-tumor injection of CAdVEC, an oncolytic adenovirus that is designed to help the immune system including HER2 specific CAR T cell react to the tumor. The study is looking at combining these two treatments together, because we think that the combination of treatments will work better than each treatment alone. We also hope to learn the best dose level of the treatments and whether or not it is safe to use them together. In this study, CAdVEC will be injected into participants tumor at one tumor site which is most easiest to reach. Once it infects the cancer cells, activation of the immune response will occur so it can attack and kill cancer cells. (This approach may have limited effects on the other tumor sites that have not received the oncolytic virus injection, so, patients will also receive specific T cells following the intratumor CAdVEC injection.) These T cells are special infection-fighting blood cells that can kill cells infected with viruses and tumor cells. Investigators want to see if these cells can survive in the blood and affect the tumor. Both CAdVEC and HER2-specific autologous CAR T are investigational products. They are not approved by the FDA.
Check if I qualifyExtracted eligibility criteria
Cancer type
Urothelial Carcinoma
Head and Neck Squamous Cell Carcinoma
Non-Small Cell Lung Carcinoma
Breast Carcinoma
Gastric Cancer
Esophageal Carcinoma
Colorectal Cancer
Pancreatic Cancer
Tumor Agnostic
Biomarker criteria
Required: HER2 (ERBB2) overexpression (IHC ≥2+ staining with CB11 or 4B5 antibody in >10% tumor cells)
HER2 positivity is defined as ≥2+ staining by IHC with either the FDA-approved CB11 antibody (Leica) or anti HER2/neu (4B5) (VENTANA), which refers to greater than weak-to-moderate staining intensity in >10% tumor cells
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Lab requirements
Blood counts
absolute neutrophil count (anc) ≥1.0 x 10^9/l; hemoglobin ≥7 g/dl; platelet count ≥ 100 x 10^9/l; pt or ptt ≤ 1.5 x uln unless the subject is receiving anticoagulation
Kidney function
serum creatinine <2 x the uln or creatinine clearance >60 ml/min
Liver function
bilirubin < 2 x uln, and ast and alt < 3 x uln
Cardiac function
lvef ≥55%
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Baylor St. Luke's Medical Center · Houston, Texas
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