drugset / Trial / NCT03333694

Safety, Tolerability, and Efficacy Study of CLL442 in Patients With Cutaneous Squamous Cell Carcinoma in Situ (SCCis)

NCT03333694 ↗

Phase 1 Terminated 40 enrolled Novartis Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
Subject CLL442 Unknown — Topical