CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 93 enrolled
Drug / intervention
Placebo +2 moredrug
Likely dose
Placebo 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02844777
NCT02844777Phase 2Completed

Randomized, Double-Blind, Placebo-Controlled, Parallel-Cohort Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Once-Daily Application of Topical VDA-1102 Ointment for 28 Days in Subjects With Actinic Keratosis

Vidac Pharma·interventional·Posted Jul 26, 2016·Updated Jan 12, 2023

In Brief

A Phase 2 clinical trial evaluating Placebo, 5% VDA-1102, and 1 other intervention for Actinic Keratosis. Completed, enrolled 93 participants across 1 site.

Detailed Summary

This Phase 2 clinical trial is a multi-center, randomized, double-blind, placebo-controlled, multiple-dose, parallel-cohort study to assess the efficacy, safety and tolerability of VDA-1102 in the treatment of actinic keratosis (AK) on the head of male and female adult subjects.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedJul 26, 2016
Enrollment StartJul 15, 2016
Primary CompletionMay 26, 2017
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 9.9 years ago

Interventions

Placebodrug

200 mg applied once-daily for 28 days

5% VDA-1102drug

200 mg applied once-daily for 28 days

10% VDA-1102drug

200 mg applied once-daily for 28 days