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Completed Phase 1Phase 2 Interventional Results available

GP2013 in the Treatment of RA Patients Refractory to or Intolerant of Standard Therapy

ClinicalTrials.gov ID: NCT01274182

Public ClinicalTrials.gov record NCT01274182. 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 21, 2026, 7:28 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 Randomized, Double-blind, Controlled Study to Evaluate PK, PD, Safety and Efficacy of GP2013 and Rituximab in Patients With Rheumatoid Arthritis Refractory or Intolerant to Standard DMARDs and up to Three Anti-TNF Therapies.

Brief summary

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

The purpose of this study is to determine the PK/PD, efficacy and safety of GP2013 in patients with severe rheumatoid arthritis.

Study identification

NCT ID
NCT01274182
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Sandoz
Industry
Enrollment
312 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
Jan 2011 (Type not available)
Primary completion
Jan 2016 (Actual)
Completion
Nov 2016 (Actual)
Last update posted
Jan 24, 2018

2011 – 2016

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Miller Clinical Research Los Angeles California 90057 —
Bluegrass Community Research, Inc. Lexington Kentucky 40504 —
Klein & Associates Cumberland Maryland 21502 —
Klein & Associates Hagerstown Maryland 21740 —
Clinical Pharmacology Study Group Worcester Massachusetts 01605 —
Physician Research Collaboration, LLC Lincoln Nebraska 68516 —
Innovative Health Research Las Vegas Nevada 89128 —
DJL Clinical Research PLLC Charlotte North Carolina 28210 —
Health Research of Oklahoma Oklahoma City Oklahoma 73103 —
Altoona Center for Clinical Research Duncansville Pennsylvania 16635 —
Clinical Research Center of Reading LLC Wyomissing Pennsylvania 19610 —
Low Country Rheumatology, PA Charleston South Carolina 29406 —
Regional Health Clinical Research Rapid City South Dakota — —
West Tennessee Research Institute Jackson Tennessee 38305 —
Arthritis & Osteoporosis Center of South Texas San Antonio Texas 78232 —
The Seattle Arthritis Center Seattle Washington 98133 —

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 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01274182, 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 Jan 24, 2018 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01274182 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →