A Clinical Study of Intratumoral MVR-T3011 (T3011) Given as a Single Agent and in Combinat
This is a Phase 1/2a, open-label, study to evaluate the safety and preliminary efficacy of intratumoral T3011 given alone and in combination with intravenous pembrolizumab in partients with advanced or metastatic solid tumors.
| Condition(s) | Solid Tumor, Melanoma, HNSCC, Sarcoma, Squamous Cell Carcinoma, NSCLC |
|---|---|
| Status | Recruiting |
| Phase | Phase 1, Phase 2 |
| Study type | Interventional |
| Summary | This is a Phase 1/2a, open-label, study to evaluate the safety and preliminary efficacy of intratumoral T3011 given alone and in combination with intravenous pembrolizumab in partients with advanced or metastatic solid tumors. |
| Who can participate | Key Inclusion Criteria: 1. Age 18 years or older. 2. Disease progression after standard of care (SOC) therapy or in the opinion of 3. The Investigator unlikely to benefit from SOC therapy. Inclusion Diagnosis Phase 1 - Histologically or pathologically confirmed locally recurrent or metastatic advanced malignancy. Phase 2a Part 1 i. Arm A - locally recurrent or metastatic melanoma. Participants must have received no more than 3 prior regimens for advanced or metastatic disease. ii. Arm B - locally recurrent or metastatic HNSCC. It must also meet the following criteria: 1) Disease progression to platinum-containing chemotherapy; 2) Failure to anti-PD-1/PDL1 blockade after receiving at least 2 doses alone or in combination. iii. Arm C - Sarcoma. Participants must have received no more than th |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | ImmVira Pharma Co. Ltd |
| Locations | Gilbert, Arizona, United States; Boston, Massachusetts, United States; Boston, Massachusetts, United States; Pittsburgh, Pennsylvania, United States; Dallas, Texas, United States; Fairfax, Virginia, United States (+3 more sites) |
| Start date | 2020-09-17 |
| NCT ID | NCT04370587 |
| Official listing | https://clinicaltrials.gov/study/NCT04370587 |