drugset / Trial / NCT04925713
IFx-Hu2.0 for the Treatment of Patients With Skin Cancer
NaSingle-groupOpen-labelTreatment
Summary
One hundred patients will receive IFx-Hu2.0 on an outpatient basis at a single time point in a single lesion. These patients will be assessed for any immediate adverse reactions and at Week 4 (Day 28+/-5 days) for any delayed adverse events..
Timeline
- Start
- 2021-06-10
- Primary completion
- 2021-10-07
- Completion
- 2022-03-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IFx-Hu2.0 | Vaccine | 0.1 mg | Other |