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Completed Phase 4 Interventional Results available

A Study to Determine the Effect of Methotrexate (MTX) Dose on Clinical Outcome and Ultrasonographic Signs in Subjects With Moderately to Severely Active Rheumatoid Arthritis (RA) Treated With Adalimumab (MUSICA)

ClinicalTrials.gov ID: NCT01185288

Public ClinicalTrials.gov record NCT01185288. 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 3, 2026, 5:03 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 Multicenter, Double-Blind, Randomized, Parallel-Arm Study to Determine the Effect of Methotrexate Dose on Clinical Outcome and Ultrasonographic Signs in Subjects With Moderately to Severely Active Rheumatoid Arthritis Treated With Adalimumab (MUSICA)

Brief summary

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

This study will investigate the efficacy of both low and high doses of methotrexate (MTX) in combination with open-label adalimumab (ADA) in patients who have had an inadequate response to high dose of MTX. The study will also evaluate the pharmacokinetics and safety of the two regimens of MTX in combination with ADA in participants with rheumatoid arthritis (RA).

Study identification

NCT ID
NCT01185288
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
309 participants

Conditions and interventions

Interventions

Biological · 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, 2010
Primary completion
Dec 31, 2012
Completion
Dec 31, 2012
Last update posted
Mar 17, 2014

2010 – 2013

United States locations

U.S. sites
46
U.S. states
25
U.S. cities
43
Facility City State ZIP Site status
Site Reference ID/Investigator# 38982 Huntsville Alabama 35801
Site Reference ID/Investigator# 38686 Tuscaloosa Alabama 35406
Site Reference ID/Investigator# 42044 Mesa Arizona 85202
Site Reference ID/Investigator# 37983 Phoenix Arizona 85031
Site Reference ID/Investigator# 44823 Little Rock Arkansas 72205
Site Reference ID/Investigator# 37981 Hemet California 92543
Site Reference ID/Investigator# 40208 Long Beach California 90822
Site Reference ID/Investigator# 38423 Sacramento California 95816
Site Reference ID/Investigator# 38204 Victorville California 92395
Site Reference ID/Investigator# 40762 Walnut Creek California 94598
Site Reference ID/Investigator# 43049 Danbury Connecticut 06810
Site Reference ID/Investigator# 38687 Jacksonville Florida 32209
Site Reference ID/Investigator# 40105 Miami Florida 33169
Site Reference ID/Investigator# 38083 Sarasota Florida 34239
Site Reference ID/Investigator# 38688 Lawrenceville Georgia 30045
Site Reference ID/Investigator# 38689 Meridian Idaho 83642
Site Reference ID/Investigator# 38085 Rock Island Illinois 61201
Site Reference ID/Investigator# 40128 Springfield Illinois 62704
Site Reference ID/Investigator# 38981 Bowling Green Kentucky 42101
Site Reference ID/Investigator# 38086 Covington Louisiana 70433
Site Reference ID/Investigator# 40125 Fall River Massachusetts 02720
Site Reference ID/Investigator# 65490 Las Vegas Nevada 89102
Site Reference ID/Investigator# 40124 Clifton New Jersey 07012
Site Reference ID/Investigator# 38978 Freehold New Jersey 07728
Site Reference ID/Investigator# 40123 Voorhees Township New Jersey 08043
Site Reference ID/Investigator# 38264 Smithtown New York 11787
Site Reference ID/Investigator# 38983 The Bronx New York 10467
Site Reference ID/Investigator# 38263 Asheville North Carolina 28803
Site Reference ID/Investigator# 38261 Greenville North Carolina 27834
Site Reference ID/Investigator# 39024 Mayfield Village Ohio 44143
Site Reference ID/Investigator# 40127 Oklahoma City Oklahoma 73104
Site Reference ID/Investigator# 38202 Bend Oregon 97701
Site Reference ID/Investigator# 39023 Eugene Oregon 97401
Site Reference ID/Investigator# 38265 Duncansville Pennsylvania 16635
Site Reference ID/Investigator# 38082 Jackson Tennessee 38305
Site Reference ID/Investigator# 37980 Dallas Texas 75231
Site Reference ID/Investigator# 44888 Dallas Texas 75246
Site Reference ID/Investigator# 43050 Houston Texas 77074
Site Reference ID/Investigator# 43735 San Antonio Texas 78229
Site Reference ID/Investigator# 44344 Richmond Virginia 23294
Site Reference ID/Investigator# 40210 Seattle Washington 98101
Site Reference ID/Investigator# 38084 Seattle Washington 98122
Site Reference ID/Investigator# 38542 Seattle Washington 98133
Site Reference ID/Investigator# 38424 Spokane Washington 99204
Site Reference ID/Investigator# 38203 Tacoma Washington 98405
Site Reference ID/Investigator# 38087 Franklin Wisconsin 53132

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01185288, 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 Mar 17, 2014 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01185288 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →