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Completed Phase 2 Interventional Results available

PoC Study to Evaluate the Efficacy and Safety of Secukinumab 300 mg in Patients With Lichen Planus

ClinicalTrials.gov ID: NCT04300296

Public ClinicalTrials.gov record NCT04300296. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 6:28 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Proof of Concept Study to Evaluate the Efficacy, Safety and Tolerability of Secukinumab 300 mg Over 32 Weeks in Adult Patients With Biopsy-proven Forms of Lichen Planus Not Adequately Controlled With Topical Therapies - PRELUDE

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary purpose of the proof of concept study is to elucidate the efficacy of secukinumab in the treatment of adult patients with biopsy-proven lichen planus not adequately controlled by topical therapies, and to assess the safety and tolerability over 32 weeks.

Study identification

NCT ID
NCT04300296
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
111 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 27, 2020 (Actual)
Primary completion
Nov 16, 2021 (Actual)
Completion
May 3, 2022 (Actual)
Last update posted
Aug 22, 2023

2020 – 2022

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35233 —
Novartis Investigative Site Thousand Oaks California 91320 —
Novartis Investigative Site Cromwell Connecticut 06416 —
Novartis Investigative Site Jacksonville Florida 32224 —
Novartis Investigative Site Miami Florida 33125 —
Novartis Investigative Site Snellville Georgia 30078 —
Novartis Investigative Site Omaha Nebraska 68144 —
Novartis Investigative Site Las Vegas Nevada 89128 —
Novartis Investigative Site East Windsor New Jersey 08520 —
Novartis Investigative Site Forest Hills New York 11375 —
Novartis Investigative Site New York New York 10025 1737 —
Novartis Investigative Site Portland Oregon 97223 —
Novartis Investigative Site Charleston South Carolina 29407 —
Novartis Investigative Site Houston Texas 77030 —
Novartis Investigative Site Pflugerville Texas 78660 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04300296, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 22, 2023 · Synced Oct 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04300296 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →