Study Evaluating Long-Term Safety Of ATN-103 In Subjects With Rheumatoid Arthritis

March 10, 2016 updated by: Ablynx

An Open-Label Extension Study To Assess The Long-term Safety And Tolerability Of ATN-103 In Subjects With Rheumatoid Arthritis

This open-label extension study will allow subjects who have completed either the 3242K1-2000-WW or 3242K1-2001-JA study to receive up to an additional 48 weeks of ATN-103 treatment and will provide data on the long-term safety and tolerability of ATN-103 in subjects with rheumatoid arthritis.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
266

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Canada
      • Quebec, Canada, G1W 4R4
        • Investigational Site
    • Manitoba
      • Winnipeg, Manitoba, Canada, R3A 1M3
        • Investigational Site
    • Ontario
      • Kitchener, Ontario, Canada, N2M 5N6
        • Investigational Site
      • St. Catharines, Ontario, Canada, L2N 7E4
        • Investigational Site
      • Toronto, Ontario, Canada, M9L 3A2
        • Investigational Site
  • Hungary
      • Budapest, Hungary, 1023
        • Investigational Site
      • Budapest, Hungary, 1036
        • Investigational Site
      • Debrecen, Hungary, 4032
        • Investigational Site
  • Japan
    • Chiba
      • Nitona-cho, Chuoh-ku, Chiba-shi, Chiba, Japan
        • Investigational Site
    • Ehime
      • Bunkyoucho, Matsuyama, Ehime, Japan
        • Investigational Site
    • Fukuoka
      • Chuoh-ku, Fukuoka-shi, Fukuoka, Japan
        • Investigational Site
      • Kurume, Fukuoka, Japan
        • Investigational Site
      • Yoshio-machi Iizuka-shi, Fukuoka, Japan
        • Investigational Site
    • Gunma
      • Tohrimachi, Takasaki, Gunma, Japan
        • Investigational Site
    • Hyogo
      • Kato, Hyogo, Japan
        • Investigational Site
    • Kumamoto
      • Kumamoto-shi, Kumamoto, Japan
        • Investigational Site
    • Kyoto
      • Honmachi, Higashiyama, Kyoto, Japan
        • Investigational Site
    • Miyazaki
      • Miyazaki-city, Miyazaki, Japan
        • Investigational Site
    • Nagano
      • Nagano-shi, Nagano, Japan
        • Investigational Site
    • Nagasaki
      • Yamato, Sasebo, Nagasaki, Japan
        • Investigational Site
    • Osaka
      • Higashi-tyo, Kawachi Nagano, Osaka, Japan
        • Investigational Site
    • Saga
      • Ureshino-machi, Ureshino-shi, Saga, Japan
        • Investigational Site
    • Saitama
      • Kawagoe, Saitama, Japan
        • Investigational Site
      • Midori-cho 2 chome Tokorozawa-shi, Saitama, Japan
        • Investigational Site
    • Tokyo
      • Kawada-cho, Shinjyuku-ku, Tokyo, Japan
        • Investigational Site
      • Shinanomachi, Shinjuku, Tokyo, Japan
        • Investigational Site
    • Toyama
      • Takaoka-shi, Toyama, Japan
        • Investigational Site
  • Russian Federation
      • Kemerovo, Russian Federation, 650066
        • Investigational Site
      • Moscow, Russian Federation, 115522
        • Investigational Site
      • Novosibirsk, Russian Federation, 630008
        • Investigational Site
      • Orenburg, Russian Federation, 460018
        • Investigational Site
      • Ryazan, Russian Federation, 390026
        • Investigational Site
      • Vladimir, Russian Federation, 600023
        • Investigational Site
      • Yaroslavl, Russian Federation, 150062
        • Investigational Site
      • Yaroslavl, Russian Federation, 150003
        • Investigational Site
  • Serbia
      • Belgrade, Serbia, 11000
        • Investigational Site
      • Niska Banja, Serbia, 18205
        • Investigational Site
  • South Africa
    • Gauteng
      • Les Marais, Gauteng, South Africa, 0084
        • Investigational Site
    • KwaZulu-Natal
      • Berea, KwaZulu-Natal, South Africa, 4001
        • Investigational Site
    • Western Cape
      • Panorama, Western Cape, South Africa, 7500
        • Investigational Site
      • Pinelands, Western Cape, South Africa, 7405
        • Investigational Site
  • Switzerland
      • Chur, Switzerland, 7000
        • Investigational Site
  • United States
    • Alabama
      • Birmingham, Alabama, United States, 35216
        • Investigational Site
      • Huntsville, Alabama, United States, 35801
        • Investigational Site
    • Arizona
      • Peoria, Arizona, United States, 85381
        • Investigational Site
    • California
      • Riverside, California, United States, 92501
        • Investigational Site
      • Upland, California, United States, 91786
        • Investigational Site
    • Connecticut
      • Bridgeport, Connecticut, United States, 06606
        • Investigational Site
    • Delaware
      • Newark, Delaware, United States, 19713
        • Investigational Site
    • Florida
      • Ocala, Florida, United States, 34474
        • Investigational Site
      • Port Orange, Florida, United States, 32127
        • Investigational Site
      • Vero Beach, Florida, United States, 32960
        • Investigational Site
    • Idaho
      • Coeur d'Alene, Idaho, United States, 83814
        • Investigational Site
    • Maryland
      • Frederick, Maryland, United States, 21702
        • Investigational Site
    • Michigan
      • Lansing, Michigan, United States, 48910
        • Investigational Site
    • New Jersey
      • Freehold, New Jersey, United States, 07728
        • Investigational Site
    • North Carolina
      • Charlotte, North Carolina, United States, 28210
        • Investigational Site
      • Winston-Salem, North Carolina, United States, 27157
        • Investigational Site
    • Ohio
      • Columbus, Ohio, United States, 43213
        • Investigational Site
    • Oklahoma
      • Oklahoma City, Oklahoma, United States, 73103
        • Investigational Site
      • Tulsa, Oklahoma, United States, 74104
        • Investigational Site
    • Oregon
      • Lake Oswego, Oregon, United States, 97035
        • Investigational Site
    • South Carolina
      • Columbia, South Carolina, United States, 29204
        • Investigational Site
      • Myrtle Beach, South Carolina, United States, 29572
        • Investigational Site
    • Tennessee
      • Nashville, Tennessee, United States, 37205
        • Investigational Site
    • Texas
      • Dallas, Texas, United States, 75231
        • Investigational Site
      • San Antonio, Texas, United States, 78217
        • Investigational Site

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years to 80 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Subjects must have completed study 3242K1-2000-WW or 3242K1-2001-JA and have had no events that, in the opinion of the investigator, would preclude entry or participation in this study.

Exclusion Criteria:

  • Pregnant or nursing women.
  • Any major illness/condition or evidence of an unstable clinical condition (eg, renal, hepatic, cardiovascular, hematological, gastrointestinal, endocrine, pulmonary, immunologic [eg, Felty syndrome, human immunodeficiency virus (HIV) infection], infectious, neurological, or cerebral psychiatric disease, or evidence of demyelinating disease) that, in the investigator's judgment, will substantially increase the risk associated with the subject's developing an adverse event (AE) or serious adverse event (SAE) during the study, or preclude the evaluation of the subject's response.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NON_RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
EXPERIMENTAL: Arm 1: ATN-103_30mg
Drug: ATN-103
A single subcutaneous injection of ATN-103 every 4 weeks (approx 13 SC injections during the study)
EXPERIMENTAL: Arm 2: ATN-103_80 mg
Drug: ATN-103
A single subcutaneous injection of ATN-103 every 4 weeks (approx 13 SC injections during the study)

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Time Frame
Collection of safety data and assessments will include adverse events, treatment-emergent adverse events, injection site reactions, infections, vital signs and safety laboratory measurements.
Time Frame: 18 months
18 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Ablynx

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Director: Medical Director, MD, Ablynx NV

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
February 1, 2010

Primary Completion (ACTUAL)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
February 1, 2012

Study Completion (ACTUAL)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
February 1, 2012

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
February 2, 2010

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
February 4, 2010

First Posted (ESTIMATE)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
February 5, 2010

Study Record Updates

Last Update Posted (ESTIMATE)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
April 11, 2016

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
March 10, 2016

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
January 1, 2013

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • 3242K1-2003
  • B2271005

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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