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Completed Phase 3 Interventional

To Study Generic Calcipotriene and Betamethasone Dipropionate Topical Suspension, 0.005%/0.064%, in the Treatment of Scalp Psoriasis

ClinicalTrials.gov ID: NCT03331523

Public ClinicalTrials.gov record NCT03331523. 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 Sep 5, 2026, 3:10 PM 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 Phase III, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multiple-Site Study to Evaluate the Therapeutic Equivalence of a Generic Calcipotriene and Betamethasone Dipropionate Topical Suspension, 0.005%/0.064% (Glenmark Pharmaceuticals Ltd) to the Marketed Product Taclonex® Topical Suspension (LEO Pharma Inc.) in the Treatment of Scalp Psoriasis

Brief summary

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

This is a phase III, randomized, double-blind, placebo-controlled, parallel- group, multiple-site study to evaluate the therapeutic equivalence of generic calcipotriene and betamethasone dipropionate topical suspension, 0.005%/0.064% of Glenmark Pharmaceuticals Ltd to that of the marketed product Taclonex® topical suspension of Leo Pharma Inc. in the treatment of scalp psoriasis.

Study identification

NCT ID
NCT03331523
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
643 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
Oct 19, 2017
Primary completion
Oct 24, 2018
Completion
Oct 24, 2018
Last update posted
Dec 20, 2018

2017 – 2018

United States locations

U.S. sites
31
U.S. states
15
U.S. cities
28
Facility City State ZIP Site status
Investigational Site 24 Encinitas California 92024
Investigational Site 3 Fremont California 94538
Investigational Site 13 San Diego California 92108
Investigational Site 20 San Diego California 92123
Investigational Site 32 Santa Monica California 90404
Investigational Site 14 Denver Colorado 80220
Investigational Site 1 Miami Florida 33144
Investigational Site 30 Miami Florida 33175
Investigational Site 7 Miramar Florida 33027
Investigational Site 22 Tampa Florida 33609
Investigational Site 15 New Albany Indiana 47150
Investigational Site 10 South Bend Indiana 46617
Investigational Site 21 Louisville Kentucky 40241
Investigational Site 6 Ann Arbor Michigan 48103
Investigational Site 12 Fridley Minnesota 55432
Investigational Site 26 Saint Joseph Missouri 64506
Investigational Site 17 Henderson Nevada 89052
Investigational Site 25 Las Vegas Nevada 89128
Investigational Site 29 Forest Hills New York 11375
Investigational Site 28 Rochester New York 14623
Investigational Site 4 High Point North Carolina 27262
Investigational Site 18 Fountain Inn South Carolina 29644
Investigational Site 27 Mt. Pleasant South Carolina 29464
Investigational Site 9 Knoxville Tennessee 37922
Investigational Site 8 Nashville Tennessee 37215
Investigational Site 5 Austin Texas 78759
Investigational Site 11 College Station Texas 77845
Investigational Site 16 San Antonio Texas 78213
Investigational Site 19 San Antonio Texas 78249
Investigational Site 31 Norfolk Virginia 23507
Investigational Site 23 Richmond Virginia 23294

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03331523, 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 Dec 20, 2018 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03331523 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →