drugset / Trial / NCT01676831
Topical Resiquimod for the Treatment of Early Stage Cutaneous T Cell Lymphoma (CTCL)
Non-randomizedSingle-groupOpen-labelTreatment
Summary
The objective of this study is to explore the safety and the preliminary efficacy of two concentrations (0.06% and 0.03%)gel that is applied to lesions of early stage (IA, IB,IIA) Cutaneous T Cell Lymphoma patients. This study is supported by grant 1R01FD004092-01A1 from the Office of Orphan Products Development, FDA.
Timeline
- Start
- 2012-02
- Primary completion
- 2015-01
- Completion
- 2015-09-28
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Resiquimod | Small molecule | 0.03 % | Topical |
| Subject | Resiquimod | Small molecule | 0.06 % | Topical |