AzTrials
AzTrials

OsteoarthritisNCT02293564

Open-label Safety Extension Study of Gevokizumab in Erosive Osteoarthritis of the Hand

A study testing gevokizumab in people with Osteoarthritis, run by XOMA (US) LLC at 28 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to evaluate the long-term safety of gevokizumab in the treatment of active inflammatory, erosive osteoarthritis of the hand. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Osteoarthritis
What is being tested?
gevokizumab
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
312 participants
Where
28 sitesUnited States
Study dates
Mar 2013to Jan 2015
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Diagnosis of hand osteoarthritis
  • Joint tenderness and/or redness
  • At least one erosion by X-ray (as determined by the central reader)
  • Contraceptive measures adequate to prevent pregnancy during the study

Who cannot join

  • History of inflammatory disease other than hand erosive osteoarthritis (EOA) including: secondary post-traumatic osteoarthritis (OA); rheumatoid arthritis; spondylarthropathies; erosion of the ulnar styloid process; psoriatic arthritis; skin psoriasis; erosions of the wrist; fibromyalgia
  • History of gout, pseudogout, or hemochromatosis
  • History of allergic or anaphylactic reactions to monoclonal antibodies
  • History of recurrent or chronic systemic infections
  • Female subjects who are pregnant, planning to become pregnant, have recently delivered, or are breast-feeding
  • Other protocol-defined inclusion/exclusion criteria may apply

Trial locations and contacts

28 sites in 1 country.

28 sites in 1 country

United States28 sites
  • Study site

    Albuerque, New Mexico

  • Study site

    Austin, Texas

  • Study site

    Boulder, Colorado

  • Study site

    Charlottesville, Virginia

  • Study site

    Dallas, Texas

  • Study site

    Denver, Colorado

  • Study site

    Duncansville, Pennsylvania

  • Study site

    Franklin, Wisconsin

  • Study site

    Hagerstown, Maryland

  • Study site

    Indianapolis, Indiana

  • Study site

    Little Rock, Arkansas

  • Study site

    Miami, Florida

  • Study site

    Norfolk, Virginia

  • Study site

    Pinellas Park, Florida

  • Study site

    Portland, Oregon

  • Study site

    Raleigh, North Carolina

  • Study site

    Reno, Nevada

  • Study site

    Roseville, California

  • Study site

    Sacramento, California

  • Study site

    San Antonio, Texas

  • Study site

    Santa Monica, California

  • Study site

    Tampa, Florida

  • Study site

    Tucson, Arizona

  • Study site

    Vero Beach, Florida

  • Study site

    Waco, Texas

  • Study site

    West Palm Beach, Florida

  • Study site

    Wheaton, Maryland

  • Study site

    Wichita, Kansas

Other trials in United States

About this study

Official title: An Open-label Safety Extension Study of Gevokizumab in Active Inflammatory, Erosive Osteoarthritis of the Hand

The purpose of this study is to evaluate the long-term safety of gevokizumab in the treatment of active inflammatory, erosive osteoarthritis of the hand.

Conditions
Osteoarthritis
Being tested
gevokizumab
Keywords
Erosive Osteoarthritis, Osteoarthritis, Osteoarthritis of the Hand
Medical subject headings
Osteoarthritis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • gevokizumabDrug

    Solution for subcutaneous injection

Study groups in NCT02293564
Study groupRoleWhat they receive
gevokizumabExperimentalNot described
Receives: Drug: gevokizumab

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Treatment-emergent adverse events

    Safety analyses will involve examination of the incidence, severity, and type of treatment-emergent adverse events reported.

    Measured: Up to two years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Nov 2014 (estimated)
  2. Study startMar 2013
  3. Primary completionJan 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
312 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02293564
Sponsor's protocol ID
X052161
Status last verified
Feb 2015
First submitted
11 Nov 2014
Last updated
19 Feb 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing gevokizumab in people with Osteoarthritis, run by XOMA (US) LLC at 28 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Feb 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 28 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Treatment-emergent adverse events (time frame: Up to two years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Feb 2015; AzTrials last refreshed its copy on 8 Nov 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in