- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT00581945
Safety and Efficacy of Multiple Doses of Canakinumab (ACZ885) in Chronic Obstructive Pulmonary Disease (COPD) Patients
28. Juni 2011 aktualisiert von: Novartis
A Randomized, Double-blind, Placebo Controlled, Exploratory Study to Assess the Safety and Efficacy of Multiple Doses of ACZ885 in Chronic Obstructive Pulmonary Disease (COPD) Patients
Was to evaluate the safety, tolerability and efficacy of multiple doses of canakinumab (ACZ885) vs. placebo when administered via intravenous infusion (IV), on pulmonary function in patients with COPD
Studienübersicht
Status
Abgeschlossen
Bedingungen
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Tatsächlich)
147
Phase
- Phase 2
- Phase 1
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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California
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Anaheim, California, Vereinigte Staaten, 92801
- Novartis Investigator Site
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Los Angeles, California, Vereinigte Staaten, 90095
- Novartis Investigator Site
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Florida
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Panama City, Florida, Vereinigte Staaten, 32405
- Novartis Investigator Site
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Georgia
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Marietta, Georgia, Vereinigte Staaten, 300060
- Novartis Investigator Site
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Maryland
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Baltimore, Maryland, Vereinigte Staaten, 21224
- Novartis Investigator Site
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Michigan
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Livonia, Michigan, Vereinigte Staaten, 48152
- Novartis Investigator Site
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Minnesota
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Minneapolis, Minnesota, Vereinigte Staaten, 55402
- Novartis Investigator Site
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Nebraska
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Omaha, Nebraska, Vereinigte Staaten, 68198-5885
- Novartis Investigator Site
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New York
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Buffalo, New York, Vereinigte Staaten, 14215
- Novartis Investigator Site
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South Carolina
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Spartanburg, South Carolina, Vereinigte Staaten, 29303
- Novartis Investigator Site
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Virginia
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Richmond, Virginia, Vereinigte Staaten, 23225
- Novartis Investigator Site
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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
40 Jahre bis 80 Jahre (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Beschreibung
Inclusion Criteria:
- Male and/or female subjects from 40-80 years (inclusive) of age
- Subjects have a clinical diagnosis of COPD
- Smokers or Ex-smokers with a smoking history of at least 20 pack years
- Post-bronchodilator forced expiratory volume in 1 second (FEV1 ) at screening ≤ 50% of the predicted normal value
- Post-bronchodilator FEV1/FVC ratio < 70%
- History of at least one treated exacerbation during the 24 months year prior to screening or C-Reactive Protein (CRP) ≥3.47 mg/L,
- Subjects should have no concomitant other lung disease or significant concomitant medical conditions that would affect the subjects' safety when participating in the study, or that would be expected to impact on the results of the study
- Female subjects must have been surgically sterilized at least 6 months prior to screening or must be using two forms of contraception, or postmenopausal women
- Able to provide written informed consent prior to study participation.
- Able to communicate well with the investigator and comply with the requirements of the study.
Exclusion Criteria:
- COPD exacerbation(s) requiring treatment within 4 weeks prior to first dosing
- History of lung reduction surgery
- Any undiagnosed nodule on chest x-ray
- Presence of certain medical conditions as specified by the protocol
- Subjects requiring oral or parenteral corticosteroids equivalent to > 10 mg/day or > 20 mg every other day of prednisone or prednisolone
- Documented homozygous alpha-1 antitrypsin deficiency.
- Participation in any clinical investigation within 4 weeks prior to dosing or longer if required by local regulation.
- Donation or loss of 400 mL or more of blood within 8 weeks prior to dosing.
- A past medical history of clinically significant electrocardiogram (ECG) abnormalities or a family history of a prolonged QT-interval syndrome.
- A known hypersensitivity to drugs similar to the study drug.
- History of immunocompromise, including a positive HIV test result.
- A positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result.
- History of drug or alcohol abuse within the 12 months prior to screening or evidence of such abuse as indicated by the laboratory assays conducted during screening.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Grundlegende Wissenschaft
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Doppelt
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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Experimental: Canakinumab
Participants received an initial dose of 1 mg/kg canakinumab (ACZ885) via intravenous infusion.
Four weeks later, participants received a dose of 3 mg/kg canakinumab, and another dose of 3 mg/kg two weeks later.
Thereafter, participants received doses of 6 mg/kg every four weeks until completion of the 45-week treatment period.
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The dose of canakinumab (ACZ885) administered was individualized, based on the subject's weight pre-dose, and was administered via intravenous infusion.
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Placebo-Komparator: Placebo
Participants received a matching placebo intravenous infusion at weeks 1, 5, 7, and thereafter every four weeks until completion of the 45-week treatment period.
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Matching placebo to ACZ885 administered via intravenous infusion.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1)
Zeitfenster: Baseline, Week 25 and Week 45
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Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second.
FEV1 was measured by spirometry performed at approximately the same time of day on each visit to avoid diurnal variation.
All spirometry calibrations and evaluations followed the recommendations of the American Thoracic Society / European Respiratory Society guidelines for acceptability.
A positive change from baseline in FEV1 indicates improvement in lung function.
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Baseline, Week 25 and Week 45
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Change From Baseline in Forced Expiratory Volume in 1 Second Percent Predicted
Zeitfenster: Baseline, Week 25 and Week 45
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The FEV1 percent predicted expresses FEV1 as a percentage of the "predicted values" for participants of similar characteristics (height, age, sex, and sometimes race and weight).
A positive change from baseline in FEV1 % predicted indicates improvement in lung function.
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Baseline, Week 25 and Week 45
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Change From Baseline in Forced Vital Capacity (FVC)
Zeitfenster: Baseline, Week 25 and Week 45
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Forced Vital Capacity is the amount of air which can be forcibly exhaled from the lungs after taking the deepest breath possible.
FVC was assessed by spirometry.
A positive change from baseline in FVC indicates improvement in lung function.
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Baseline, Week 25 and Week 45
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Change From Baseline in Slow Vital Capacity (SVC)
Zeitfenster: Baseline, Week 25 and Week 45
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Vital Capacity is the amount of air that can be forcibly exhaled from the lungs after a full inhalation.
Slow Vital Capacity (SVC) test is performed by having the patient slowly and completely blow out all of the air from their lungs.
A positive change from baseline in SVC indicates improvement in lung function.
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Baseline, Week 25 and Week 45
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Change From Baseline in Forced Expiratory Flow 25% to 75%
Zeitfenster: Baseline, Week 25 and Week 45
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The forced expiratory flow (FEF) 25%-75% measurement describes the amount of air expelled from the lungs during the middle half (25% - 75%) of the forced vital capacity test and is measured using spirometry.
A positive change from baseline in FEF indicates improvement in lung function.
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Baseline, Week 25 and Week 45
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Number of Participants Who Experienced Serious Adverse Events or Discontinued Due to Adverse Events
Zeitfenster: Adverse events were collected during the 45 week treatment period and the 12 week follow-up period.
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Safety was assessed by the number of participants with serious adverse events and/or adverse events leading to study discontinuation.
A summary of adverse events is presented with this outcome, additional details are provided in the Adverse Events section.
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Adverse events were collected during the 45 week treatment period and the 12 week follow-up period.
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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
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. Januar 2007
Primärer Abschluss (Tatsächlich)
1. Mai 2010
Studienabschluss (Tatsächlich)
1. Mai 2010
Studienanmeldedaten
Zuerst eingereicht
21. Dezember 2007
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
21. Dezember 2007
Zuerst gepostet (Schätzen)
28. Dezember 2007
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
30. Juni 2011
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
28. Juni 2011
Zuletzt verifiziert
1. Juni 2011
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- CACZ885B2204
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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