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Completed Phase 2 Interventional Results available

A Study to Evaluate the Efficacy and Safety of DC-806 in Participants With Moderate to Severe Plaque Psoriasis

ClinicalTrials.gov ID: NCT05896527

Public ClinicalTrials.gov record NCT05896527. 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 17, 2026, 9:55 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 Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Dose-ranging Study to Evaluate the Efficacy and Safety of DC-806 in Participants With Moderate to Severe Plaque Psoriasis

Brief summary

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

This was a 12-week treatment, multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-ranging study to evaluate the efficacy and safety of DC-806 in participants with moderate to severe plaque psoriasis. This study evaluated the efficacy, safety, tolerability, and pharmacokinetics (PK) of multiple oral doses of DC-806 in participants with moderate to severe plaque psoriasis.

Study identification

NCT ID
NCT05896527
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
229 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
May 2, 2023 (Actual)
Primary completion
Mar 25, 2024 (Actual)
Completion
Mar 25, 2024 (Actual)
Last update posted
Apr 4, 2025

2023 – 2024

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
First OC Dermatology Fountain Valley California 92708-3701 —
Clinical Science Institute Santa Monica California 90404-2120 —
Driven Research LLC Coral Gables Florida 33134-3901 —
Kirsch Dermatology - Probity - PPDS Naples Florida 34102-6538 —
GCP Global Clinical Professionals, LLC St. Petersburg Florida 33713-8012 —
ForCare Clinical Research - CenExel FCR - PPDS Tampa Florida 33613-1244 —
The Indiana Clinical Trials Center, PC Plainfield Indiana 46168-2792 —
Dermatology Specialists Research - 501 S 2nd St Louisville Kentucky 40202-2862 —
DICE Therapeutics Study Site New York New York 10003-3314 —
Dermatologists of Southwest Ohio - Probity - PPDS Mason Ohio 45040-4520 —
Paddington Testing Company Inc Philadelphia Pennsylvania 19103-4738 —
Center for Clinical Studies - Webster Webster Texas 77598-4927 —
Virginia Clinical Research Inc Norfolk Virginia 23502-3945 —

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 43 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05896527, 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 Apr 4, 2025 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05896527 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →