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Effect of Febuxostat on Joint Damage in Hyperuricemic Subjects With Early Gout

3. September 2014 aktualisiert von: Takeda

A Multicenter, Randomized, Double-Blind, Phase 2 Study to Evaluate the Effect of Febuxostat Versus Placebo in Joint Damage in Hyperuricemic Subjects With Early Gout

This purpose of this study is to assess the effect of febuxostat, once daily (QD), on joint damage in patients with elevated serum urate levels and gout.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

Gout is caused by high levels of uric acid in the body, and is associated with a broad range of comorbidities including heart disease, chronic kidney disease and additional risk factors like obesity and high blood pressure. Hyperuricemia, which is defined as an elevation in serum urate levels, develops into gout when urate crystals form from supersaturated body fluids and settle in joints and other organs. Urate-lowering therapy is used to treat hyperuricemia in patients with gout.

Current treatments focus on initiating urate-lowering therapy in hyperuricemic gout patients who have experienced multiple acute gout flares within the past year. However, joint damage caused by crystal deposition may occur much earlier than previously considered. Monosodium urate crystals have been found present in the joints of people with hyperuricemia who do not have any symptoms. The presence of monosodium urate crystals would indicate that after the crystals form, they stay within the joint if serum urate levels are not reduced. Lowering uric acid levels and maintaining them may reduce acute gout flare episodes and possibly halt or reduce joint damage in patients with gout.

This study will evaluate the effect of febuxostat on joint damage in hyperuricemic patients with early gout. All patients will receive gout flare prophylaxis for the first 6 months of the study. Gout flares may also be treated throughout the study.

A variety of imaging techniques are in use to evaluate gout. Plain radiographs (x-rays), Magnetic Resonance Imaging (MRI) and Dual Energy Computed Tomography (DECT) will be utilized in this study. The modified Sharp/Van Der Heijde scoring method (named after Drs. Sharp and Van Der Heijde) for assessment of x-rays has been validated in patients with chronic gout and will be used in this study for evaluating erosion and joint space narrowing. Participants are expected to have 15 visits which will include plain radiographic examinations at 5 visits, 3 Magnetic Resonance Imaging (MRI) examinations and 3 DECT procedures at selected sites.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

314

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

  • Vereinigte Staaten
    • Arizona
      • Mesa, Arizona, Vereinigte Staaten
      • Tucson, Arizona, Vereinigte Staaten
    • California
      • Burbank, California, Vereinigte Staaten
      • Carmichael, California, Vereinigte Staaten
      • Costa Mesa, California, Vereinigte Staaten
      • Irvine, California, Vereinigte Staaten
      • Orange, California, Vereinigte Staaten
      • Rancho Cucamonga, California, Vereinigte Staaten
      • San Diego, California, Vereinigte Staaten
      • San Luis Obispo, California, Vereinigte Staaten
    • Connecticut
      • Trumbull, Connecticut, Vereinigte Staaten
    • Florida
      • Boynton Beach, Florida, Vereinigte Staaten
      • Daytona Beach, Florida, Vereinigte Staaten
      • Fort Lauderdale, Florida, Vereinigte Staaten
      • Hialeah, Florida, Vereinigte Staaten
      • Miami, Florida, Vereinigte Staaten
      • Sanford, Florida, Vereinigte Staaten
      • Tampa, Florida, Vereinigte Staaten
      • Winter Park, Florida, Vereinigte Staaten
    • Hawaii
      • Honolulu, Hawaii, Vereinigte Staaten
    • Illinois
      • Arlington Heights, Illinois, Vereinigte Staaten
    • Indiana
      • Avon, Indiana, Vereinigte Staaten
      • Greenfield, Indiana, Vereinigte Staaten
    • Kansas
      • Wichita, Kansas, Vereinigte Staaten
    • Maine
      • Rockport, Maine, Vereinigte Staaten
    • Minnesota
      • Chaska, Minnesota, Vereinigte Staaten
    • Mississippi
      • Belzoni, Mississippi, Vereinigte Staaten
      • Olive Branch, Mississippi, Vereinigte Staaten
    • Montana
      • Billings, Montana, Vereinigte Staaten
      • Missoula, Montana, Vereinigte Staaten
    • Nebraska
      • Bellevue, Nebraska, Vereinigte Staaten
    • Nevada
      • Henderson, Nevada, Vereinigte Staaten
      • Las Vegas, Nevada, Vereinigte Staaten
    • New Mexico
      • Albuquerque, New Mexico, Vereinigte Staaten
    • North Carolina
      • Charlotte, North Carolina, Vereinigte Staaten
      • Lenoir, North Carolina, Vereinigte Staaten
      • Shelby, North Carolina, Vereinigte Staaten
    • Ohio
      • Dayton, Ohio, Vereinigte Staaten
      • Franklin, Ohio, Vereinigte Staaten
      • Willoughby Hills, Ohio, Vereinigte Staaten
    • Oklahoma
      • Oklahoma City, Oklahoma, Vereinigte Staaten
    • Oregon
      • Eugene, Oregon, Vereinigte Staaten
    • Pennsylvania
      • Duncansville, Pennsylvania, Vereinigte Staaten
    • Rhode Island
      • East Providence, Rhode Island, Vereinigte Staaten
    • South Carolina
      • Columbia, South Carolina, Vereinigte Staaten
    • South Dakota
      • Rapid City, South Dakota, Vereinigte Staaten
    • Tennessee
      • Kingsport, Tennessee, Vereinigte Staaten
    • Texas
      • Austin, Texas, Vereinigte Staaten
      • Houston, Texas, Vereinigte Staaten
      • San Antonio, Texas, Vereinigte Staaten
      • Southlake, Texas, Vereinigte Staaten
      • Sugar Land, Texas, Vereinigte Staaten
    • Virginia
      • Arlington, Virginia, Vereinigte Staaten
      • Burke, Virginia, Vereinigte Staaten
      • Manassas, Virginia, Vereinigte Staaten
    • Wisconsin
      • Kenosha, Wisconsin, Vereinigte Staaten

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • The participant, or the participant's legally acceptable representative, signs a written informed consent form/Health Insurance Portability & Accountability Act (HIPAA) Authorization prior to the initiation of any study procedures.

  • Must have a history or presence of gout defined as having one or more of the following conditions of the American Rheumatism Association (ARA) preliminary criteria for the diagnosis of gout

    • A tophus proven to contain urate crystals by chemical or polarized light microscopic means and/or
    • Characteristic urate crystals in the joint fluid and/or

    • History of at least 6 of the following clinical, laboratory and x-ray phenomena*: *More than one flare criteria will be excluded for the purpose of this study if the participant has a history of only a single acute gout flare.

      • More than one attack of acute arthritis*
      • maximum inflammation developed within 1 day
      • monoarticular arthritis
      • redness observed over joints
      • first metatarsophalangeal joint painful or swollen
      • unilateral first metatarsophalangeal joint attack
      • unilateral tarsal joint attack
      • tophus (proven or suspected)
      • hyperuricemia
      • asymmetric swelling within a joint on x-ray
      • sub-cortical cysts without erosions on x-ray
      • joint fluid culture negative for organisms during attacks
    • *More than one flare criteria will be excluded for the purpose of this study if the participant has a history of only a single acute gout flare.

  • Is male and at least 18 years of age OR;

    • Female ≥45 years of age and at least 2 years post-menopausal AND has a Follicle Stimulating Hormone (FSH) level ≥40 IU/L OR
    • Female receiving hormone replacement therapy (HRT) must be ≥55 years of age (FSH level not required).
  • Has hyperuricemia defined as serum Uric Acid (sUA) level ≥7.0 mg/dL at Screening.
  • Has a history of ≤2 (1 or 2) flares. In participants with a history of 2 flares, must have had only one flare in any 12 month period. The primary affected joint will be based on the location of the first gout flare which must be located within right or left metatarsophalangeal (MTP), interphalangeal (IP), ankle, metacarpophalangeal (MCP), Proximal Inter-Phalangeal (PIP), or distal inter-phalangeal (DIP) joints prior to Screening.
  • Is capable of understanding and complying with protocol requirements, including scheduled clinic procedures.

Exclusion Criteria:

  • Previously on urate-lowering therapy (allopurinol, febuxostat or probenecid).
  • Has secondary hyperuricemia (eg due to myeloproliferative disorder or organ transplant).
  • Has a history of xanthinuria.
  • Has a known hypersensitivity to any component of the febuxostat formulation.
  • Has rheumatoid arthritis.
  • Has active peptic ulcer disease.
  • Has a history of cancer, except basal cell carcinoma of the skin, which has not been in remission for at least 5 years prior to the first dose of study medication.
  • Has experienced either a myocardial infarction (MI) or stroke within 90 days prior to the Screening visit.
  • Has alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) values greater than 2.0 the upper limit of normal during the Screening period.
  • Has a significant medical condition and/or conditions that would interfere with the treatment, safety or compliance with the protocol at the discretion of the Investigator.
  • Has a history of drug abuse (defined as any illicit drug use) or a history of alcohol abuse with 5 years prior to the Screening visit. Participant consumes >14 alcoholic beverages/week.
  • Has received any investigational medicinal product within 30 days prior to the Screening visit. In addition, the participant has been previously randomized into this study and received at least one dose of double blind study drug treatment.
  • Has an estimated Glomerular filtration rate (eGFR) <60 mL/min calculated using the Modification of Diet in Renal Disease (MDRD) formula by the Central Laboratory.
  • Has a serum creatinine at Screening greater than 2.0 mg/dL.
  • Has a known history of infection with hepatitis B, hepatitis C or human immunodeficiency virus.
  • Is a study site employee, or is an immediate family member (ie, spouse, parent, child, and sibling) of a study site employee involved in conduct of this study.
  • Is unable to understand verbal or written English or any other language for which a certified translation of the approved informed consent form is available.
  • Is required to take excluded medications.

  • Magnetic Resolution Imaging:

    • Has a known hypersensitivity to gadolinium
    • Has history of severe asthma
    • Has an electronically, magnetically or mechanically activated implanted device
    • Has any object that could present a potential hazard or interfere with MRI interpretation secondary to the artifact (i.e. metallic foreign bodies)
    • Has a significant medical condition considered by the Investigator (or radiologist) to interfere with the participant's ability to receive gadolinium (eg Sickle cell anemia).

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Febuxostat 40 mg or 80 mg
Febuxostat 40 mg or 80 mg (based on serum urate levels at Day 14), capsules, orally, once daily for up to 24 Months.
Arzneimittel: Febuxostat
Febuxostat-Kapseln
Andere Namen:
  • Ulorisch
  • TMX-67
Placebo-Komparator: Placebo
Febuxostat placebo-matching capsules, orally, once daily for up to 24 Months.
Arzneimittel: Placebo for Febuxostat
Febuxostat placebo-matching capsules

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Mean Change From Baseline to Month 24 in the Modified Sharp/Van Der Heijde Erosion Score of the Single Affected Joint
Zeitfenster: Baseline and Month 24
The single affected joint was defined as the joint with the history of the first acute gout flare. Radiographs (X-rays) of this single joint in the hands or feet were evaluated using the modified Sharp/van der Heijde method. Each erosion was assessed using a 4-point scale where 0=no erosions (best) to 3=large erosion passing the mid-line (worst). Individual erosion scores were summed to a maximum erosion score of 5 for joints in the hands and 10 for joints in the feet. Higher scores indicated more joint damage. A negative change from Baseline indicated improvement.
Baseline and Month 24

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Mean Change From Baseline to Month 24 in the Modified Sharp/Van Der Heijde Total Scores From Full Hands and Feet Radiographs
Zeitfenster: Baseline and Month 24
Radiographs (X-rays) of 40 joints in the hands and 12 joints in the feet were evaluated using the modified Sharp/van der Heijde method. Each erosion was assessed using a 4-point scale where 0=no erosions (best) to 3=large erosion passing the mid-line (worst) for a total erosion score range of 0 to 320. Joint space narrowing (JSN) was assessed using a 5-point scale where 0=normal (best) to 4=absence of joint space, presumptive evidence of ankyloses, or complete luxation (worst) for a total JSN score range of 0 to 208. The Erosion Score and the JSN Score were combined for a total possible score of 0 to 528. Higher scores indicated more joint damage. A negative change from Baseline indicated improvement.
Baseline and Month 24
Mean Change From Baseline to Month 24 in the Modified Sharp/Van Der Heijde Erosion Scores From Full Hands and Feet Radiographs
Zeitfenster: Baseline and Month 24
Radiographs (X-rays) of 40 joints in the hands and 12 joints in the feet were evaluated using the modified Sharp/van der Heijde method. Each erosion was assessed using a 4-point scale where 0=no erosions (best) to 3=large erosion passing the mid-line (worst) for a total erosion score range of 0 to 320. Higher scores indicated more joint damage. A negative change from Baseline indicated improvement.
Baseline and Month 24
Mean Change From Baseline to Month 24 in the Rheumatoid Arthritis MRI Scoring System (RAMRIS) Score of the Single Affected Joint
Zeitfenster: Baseline and Month 24
The single affected joint was defined as the joint with the history of the first acute gout flare. Magnetic Resonance Imaging (MRI) was evaluated using the Rheumatoid Arthritis MRI Score (RAMRIS). Bone erosion in the proximal and distal location were each assessed in the affected joint using an 11-point scale where 0=no erosion (best) to 10=91-100% bone eroded (worst) for a bone erosion score range of 0 to 20. Bone marrow edema in the proximal and distal location were each assessed using a 4-point scale where 0=no edema (best) to 3=67-100% edema (worst) for a bone marrow edema (BME) score range of 0 to 6. Synovitis was assessed in the affected joint using a 4-point scale where 0=normal (best) to 3=severe (worst). Higher scores indicated more joint damage. A negative change from Baseline indicated improvement.
Baseline and Month 24
Mean Change From Baseline to Month 24 in the Modified Sharp/Van Der Heijde Total Score of the Single Affected Joint
Zeitfenster: Baseline and Month 24
The single affected joint was defined as the joint with the history of the first acute gout flare. Radiographs (X-rays) of the single affected joint in the hands or feet were evaluated using the modified Sharp/van der Heijde method. Each erosion was assessed using a 4-point scale where 0=no erosions (best) to 3=large erosion passing the mid-line (worst) and Joint space narrowing (JSN) was assessed using a 5-point scale where 0=normal (best) to 4=absence of joint space, presumptive evidence of ankyloses, or complete luxation (worst). The Erosion Score and the JSN Score were summed for the Total Score. Higher scores indicated more joint damage. A negative change from Baseline indicated improvement.
Baseline and Month 24

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Takeda

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Nützliche Links

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. März 2010

Primärer Abschluss (Tatsächlich)

1. September 2013

Studienabschluss (Tatsächlich)

1. September 2013

Studienanmeldedaten

Zuerst eingereicht

26. Februar 2010

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

1. März 2010

Zuerst gepostet (Schätzen)

2. März 2010

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

10. September 2014

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

3. September 2014

Zuletzt verifiziert

1. September 2014

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • TMX-67_204
  • U1111-1113-8098 (Registrierungskennung: WHO)

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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