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Completed Phase 3 Interventional Results available

Phase 3 Study of M923 and Humira® in Subjects With Chronic Plaque-type Psoriasis

ClinicalTrials.gov ID: NCT02581345

Public ClinicalTrials.gov record NCT02581345. 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 Nov 7, 2026, 2:48 PM EST

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Official title

A Phase 3 Randomized, Double-blind, Multicenter Study to Evaluate Efficacy, Safety, and Immunogenicity of an Adalimumab Biosimilar (M923) and Humira® in Subjects With Moderate to Severe Chronic Plaque-type Psoriasis

Brief summary

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

The purpose of the study is to evaluate efficacy, safety, and immunogenicity of a proposed adalimumab biosimilar (M923) and Humira in participants with moderate to severe chronic plaque-type psoriasis.

Study identification

NCT ID
NCT02581345
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Momenta Pharmaceuticals, Inc.
Industry
Enrollment
572 participants

Conditions and interventions

Interventions

Biological

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
Sep 2015 (Type not available)
Primary completion
Apr 4, 2017 (Actual)
Completion
Apr 4, 2017 (Actual)
Last update posted
Oct 17, 2018

2015 – 2017

United States locations

U.S. sites
24
U.S. states
11
U.S. cities
23
Facility City State ZIP Site status
Wallace Medical Group, Inc. Beverly Hills California 90211 —
Encino Research Center Encino California 91436 —
eStudySite La Mesa California 91942 —
eStudySite Oceanside California 92056 —
eStudySite San Diego California 92120 —
Shahram Jacobs MD, INC Sherman Oaks California 91403 —
Horizons Clinical Research Center, LLC Denver Colorado 80220 —
Bioclinical Research Alliance; Inc Miami Florida 33155 —
Sanitas Reasearch, LLC Miami Florida 33155 —
Renstar Medical Research Ocala Florida 34471 —
Compass Research, LLC Orlando Florida 32806 —
Dawes Fretzin Clinical Research Group, LLC Indianapolis Indiana 46256 —
Radiant Research; Inc. Overland Park Kansas 66210 —
Tufts Medical Center; Inc. Boston Massachusetts 02111 —
Bay State Clinical Trials, Inc Watertown Massachusetts 02472 —
eStudySite Las Vegas Nevada 89109 —
Radiant Research; Inc. Cincinnati Ohio 45249 —
Radiant Research, Inc. Columbus Ohio 43212 —
Radiant Clinical Research Anderson South Carolina 29621 —
Palmetto Clinical Trial Services, LLC Fountain Inn South Carolina 29644 —
Radiant Research, Inc. Greer South Carolina 29650 —
Austin Institute for Clinical Research, LLC Pflugerville Texas 78660 —
Clinical Trials of Texas; Inc. San Antonio Texas 78229 —
National Clinical Research-Richmond, Inc 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 66 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02581345, 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 Oct 17, 2018 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02581345 live on ClinicalTrials.gov.

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