ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Efficacy and Safety Study of Apremilast (CC-10004) in Subjects With Moderate-to-Severe Plaque-Type Psoriasis (Core Study)

ClinicalTrials.gov ID: NCT00773734

Public ClinicalTrials.gov record NCT00773734. 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 May 5, 2026, 2:34 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 Phase 2B, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging, Efficacy and Safety Study of Apremilast (CC-10004) in Subjects With Moderate-to-Severe Plaque-Type Psoriasis (Core Study)

Study identification

NCT ID
NCT00773734
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Amgen
Industry
Enrollment
352 participants

Conditions and interventions

Interventions

  • Apremilast 10mg Drug
  • Apremilast 20mg Drug
  • Apremilast 30 mg Drug
  • Apremilast 30mg Drug
  • Placebo Drug

Drug

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
Aug 31, 2008
Primary completion
Jul 31, 2009
Completion
May 19, 2015
Last update posted
May 6, 2020

2008 – 2015

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Associates In Research Inc Fresno California 93720
Dermatology Associates Los Angeles California 90045
Stanford University School of Medicine Redwood City California 94063
Atlantic Skin & Cosmetic Surgery Group, PC Wilmington Delaware 19810
Renstar Medical Research Ocala Florida 34471
Atlanta Dermatology, Vein & Research Center Alpharetta Georgia 30022
NorthShore University HealthSystem Skokie Illinois 60077
Dawes/Fretzin Dermatology Group Inc Indianapolis Indiana 46256
Dermatology & Advanced Aesthetics Lake Charles Louisiana 70605
Minnesota Clinical Study Center Fridley Minnesota 55432
Central Dermatology St Louis Missouri 63117
UMDNJ Robert Wood Johnson New Brunswick New Jersey 08901
Wright State University Dayton Ohio 45408
Allergy, Asthma and Dermatology Research Center Lake Oswego Oregon 97035
Northwest Cutaneous Research Specialists Portland Oregon 97210
Oregon Med. Research Center, PC Portland Oregon 97223
Rivergate Dermatology Clinical Research Goodlettsville Tennessee 37072
Modern Research Associates Dallas Texas 75231
Dermatology Associates of Seattle Seattle Washington 98101
Aurora Advanced Healthcare, Inc Milwaukee Wisconsin 53209

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 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00773734, 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 May 6, 2020 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00773734 live on ClinicalTrials.gov.

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