drugset / Trial / NCT03333694
Safety, Tolerability, and Efficacy Study of CLL442 in Patients With Cutaneous Squamous Cell Carcinoma in Situ (SCCis)
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this first in human and proof of concept study is to characterize the safety, tolerability and initial efficacy of CLL442 in patients with Squamous Cell Carcinoma in situ (SCCis) to enable further clinical development of CLL442.
Timeline
- Start
- 2017-12-15
- Primary completion
- 2018-11-01
- Completion
- 2018-11-01
Outcome
Outcome not reported
Stopped (Enrollment): “The study fully enrolled and completed after last patient completed the study”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CLL442 | Unknown | — | Topical |