- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01417091
Safety, Pharmacokinetics and Pharmacodynamics of BPS804 in Osteogenesis Imperfecta
A Randomized, Open Label Intra-patient Dose Escalation Study With an Untreated Reference Group to Evaluate Safety and Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Infusions of BPS804 in Adults With Moderate Osteogenesis Imperfecta
This is a randomized, open label intra-patient dose escalation study to evaluate safety and tolerability, pharmacokinetics, and pharmacodynamics of BPS804 in adults with osteogenesis imperfecta (OI).
Pharmacodynamic effect will be determined by serological biomarkers and radiologic assessments. In addition, tolerability and pharmacokinetics (PK) will be evaluated.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Phase 2
Kontakte und Standorte
Studienorte
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Bruxelles, Belgien, 1200
- Novartis Investigative Site
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Gent, Belgien, 9000
- Novartis Investigative Site
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Wuerzburg, Deutschland, 97074
- Novartis Investigative Site
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Quebec
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Montreal, Quebec, Kanada, H3GIA6
- Novartis Investigative Site
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California
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Anaheim, California, Vereinigte Staaten, 92801
- Novartis Investigative Site
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Florida
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Miramar, Florida, Vereinigte Staaten, 33025
- Novartis Investigative Site
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Osteogenesis imperfecta
- Two or more previous fractures
- Bone mineral density Z-score of ≤ -1.0 and > -4.0
Exclusion Criteria:
- Open epiphyses
- Fracture within last 2 weeks
- Treatment with bisphosphonates/teriparatide (last 6 months)
- Surgery within last year
Other protocol-defined inclusion/exclusion criteria may apply
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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Experimental: Behandlungsgruppe
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Kein Eingriff: Untreated reference group
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Safety and tolerability (composite outcome: standard laboratory, (serious) adverse events)
Zeitfenster: Day 1 through 141
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The assessment of safety will be based on primarily on the frequency of adverse events, laboratory abnormalities, and serious adverse events suspected by the investigators to be related to study treatments.
The AE collection period extends from the time of first study drug administration drug until study completion.
The intensity of each AE will be characterized and classified into 1 of the 3 generic categories (mild, moderate, or severe).
The number and percentage of patients with adverse events will be tabulated by treatment group, body system and preferred term.
The periods for adverse event tabulation will be from dose administration up to next dose administration if a further dose is given, and from dose administration to EOS for the last dose administration of a patient.
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Day 1 through 141
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Determination of pharmacodynamic effect by means of biomarkers
Zeitfenster: Day 1 and Day 43
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Biomarker data from serum bone formation biomarkers: procollagen type I N-terminal propeptide, procollagen type I C-terminal propeptide, osteocalcin, and bone-specific alkaline phosphatase, and from serum bone resporption mbiomarkers: C-telopeptides of type I collagen cross-links, and N-telopeptides of type I collagen cross-links will be reported as concentration results, measured using a specific assay with a working range defined by the Lower limit of quantification and Upper limit of quantification.
It will be considered a sign for efficacy, if any of the above show significant (2-sided, alpha=0.05)
increase versus baseline in the BPS804 group on day 43.
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Day 1 and Day 43
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Change in Z-score from baseline to Day 141
Zeitfenster: Day 1 and Day 141
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Bone mineral density will be assessed by dual-energy X-ray absorptiometry of the lumbar spine.
Analysis will include four vertebral levels from L1 to L4.
Individual vertebral levels may be excluded due to artifact.
Bone mineral density Z-scores will be used as these are a comparison of a patient's BMD to that of a patient of the same age, sex, and ethnicity.
The comparison of change from baseline with the matching change in the reference group will be done by 2-sample t-tests (1-sided).
It will be considered a sign for efficacy, if any of the above show significant (2-sided, alpha=0.05)
increase versus baseline in the BPS804 group on day 141.
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Day 1 and Day 141
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Determination of the serum concentration-time profiles of BPS804
Zeitfenster: Day 1 (prior to administration and 3x after administration) and Days 2, 8, 15 (2x), 16, 29 (4x), 30, 36, 43, 57, 85, 113,141
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Individual and overlaying individual serum concentration-time profiles of BPS804 will be constructed from the serial sampling on Day 1 (prior to administration and 3x after administration) and Days 2, 8, 15 (2x), 16, 29 (4x), 30, 36, 43, 57, 85, 113,141.
In addition arithmetic and geometric mean serum concentration-time profiles of BPS804 will be constructed from the above data points.
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Day 1 (prior to administration and 3x after administration) and Days 2, 8, 15 (2x), 16, 29 (4x), 30, 36, 43, 57, 85, 113,141
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Determination of the area under the serum concentration-time curve from time zero to the end of the dosing interval tau after the first dose
Zeitfenster: Day 1 (prior to administration and 3x after administration) and Days 2, and 8
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The area under the serum concentration-time curve from time zero to the end of the dosing interval tau after the first dose will be derived using using non-compartmental methods from data collected on Day 1 (4x) and Days 2, and 8.
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Day 1 (prior to administration and 3x after administration) and Days 2, and 8
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Determination of the maximal concentration after the first dose
Zeitfenster: Day 1 (prior to administration and 3x after administration) and Days 2, and 8
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The maximal concentration after the first dose will be derived using using non-compartmental methods from data collected Day 1 (4x) and Days 2, and 8.
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Day 1 (prior to administration and 3x after administration) and Days 2, and 8
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Determination of the time of maximal concentration after the first dose
Zeitfenster: Day 1 (prior to administration and 3x after administration) and Days 2, and 8
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The time of maximal concentration after the first dose will be derived using using non-compartmental methods from data collected Day 1 (4x) and Days 2, and 8.
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Day 1 (prior to administration and 3x after administration) and Days 2, and 8
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Determination of the maximal concentration after the second dose
Zeitfenster: Day 15 (prior to administration and 1x after administration) and Day 16
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The maximal concentration after the second dose will be derived using using non-compartmental methods from data collected from days 15 (2x) and 16.
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Day 15 (prior to administration and 1x after administration) and Day 16
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Determination of the time of maximal concentration after the second dose
Zeitfenster: Day 15 (prior to administration and 1x after administration) and Day 16
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The time of maximal concentration after the second dose will be derived using using non-compartmental methods from data collected from days 15 (2x) and 16.
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Day 15 (prior to administration and 1x after administration) and Day 16
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Determination of the area under the serum concentration-time curve from time zero to infinity after the third dose
Zeitfenster: Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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The area under the serum concentration-time curve from time zero to the end of the dosing interval tau after the third dose will be derived using non-compartmental methods from data collected on Days 29 (4x), 30, 36, 43, 57, 85, 113, and 141.
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Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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Determination of the area under the serum concentration-time curve from time zero to the time of the last quantifiable concentration after the third dose
Zeitfenster: Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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The area under the serum concentration-time curve from time zero to the time of the last quantifiable concentration after the third dose will be derived using non-compartmental methods from data collected on Days 29 (4x), 30, 36, 43, 57, 85, 113, and 141.
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Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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Determination of the area under the serum concentration-time curve from time zero to the end of the dosing interval tau after the third dose
Zeitfenster: Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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The area under the serum concentration-time curve from time zero to the end of the dosing interval tau after the third dose will be derived using non-compartmental methods from data collected on Days 29 (4x), 30, 36, 43, 57, 85, 113, and 141.
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Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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Determination of the maximal serum concentration after the third dose
Zeitfenster: Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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The maximal serum concentration after the third dose will be derived using using non-compartmental methods from data collected on Days 29 (4x), 30, 36, 43, 57, 85, 113, and 141.
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Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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Determination of the time of maximal concentration after the third dose
Zeitfenster: Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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The time of maximal concentration after the third dose will be derived using using non-compartmental methods from data collected on Days 29 (4x), 30, 36, 43, 57, 85, 113, and 141.
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Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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Determination of the terminal elimination half-life after the third dose
Zeitfenster: Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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The terminal elimination half-life after the third dose will be derived from data collected on Days 29 (4x), 30, 36, 43, 57, 85, 113, and 141 using a compound-specific modeling approach.
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Days 29 (prior to administration and 3x after administration) and 30, 36, 43, 57, 85, 113, and 141
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Determination of the concentration of total sclerostin in serum
Zeitfenster: Screening, Days 1, 8, 15, 29, 36, 43, 57, 85, 113, 141
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The function of sclerostin is described as an endogenous negative regulator of bone formation.
Total serum sclerostin will be measured from samples collected at screening and on days 1, 8, 15, 29, 36, 43, 57, 85, 113, and 141
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Screening, Days 1, 8, 15, 29, 36, 43, 57, 85, 113, 141
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Immunogenicity evaluation in serum
Zeitfenster: Days 1, 29, 85, and 141
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Immunogenicity will only be assessed in patients randomized to the treatment group.
Anti-BPS804 antibodies will be measured in human serum on Days 1, 29, 85, and 141 An immunogenicity positive patient at end of study will be followed up until anti-BPS804 antibody levels are back to levels measured on Day 1.
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Days 1, 29, 85, and 141
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Mitarbeiter und Ermittler
Sponsor
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- CBPS804A2201
- 2011-001465-41 (EudraCT-Nummer)
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Produkt, das in den USA hergestellt und aus den USA exportiert wird
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 .
Klinische Studien zur Osteogenesis imperfecta
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Ultragenyx Pharmaceutical IncMereo BioPharmaAbgeschlossenOsteogenesis imperfecta Typ III | Osteogenesis imperfecta Typ IV | Osteogenesis imperfecta, Typ IVereinigte Staaten, Kanada, Dänemark, Frankreich, Vereinigtes Königreich
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Nationwide Children's HospitalAbgeschlossenOsteogenesis imperfecta Typ III | Osteogenesis imperfecta Typ IIVereinigte Staaten
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Emory UniversityNoch keine RekrutierungOsteogenesis imperfecta | Osteogenesis imperfecta Typ III
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Novartis PharmaceuticalsAbgeschlossenOsteogenesis imperfectaVereinigte Staaten
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Shriners Hospitals for ChildrenNovartisAbgeschlossen
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AmgenBeendetOsteogenesis imperfecta (OI)Kanada, Tschechien, Spanien, Vereinigtes Königreich, Vereinigte Staaten, Italien, Ungarn, Australien, Belgien, Frankreich, Deutschland, Polen
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Istituto Ortopedico RizzoliRekrutierungOsteogenesis imperfectaItalien
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Baylor College of MedicineRekrutierungOsteogenesis imperfectaVereinigte Staaten
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SanofiRekrutierungOsteogenesis imperfectaVereinigte Staaten, Australien, Kanada, Frankreich
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Ultragenyx Pharmaceutical IncMereo BioPharmaAktiv, nicht rekrutierendOsteogenesis imperfectaVereinigte Staaten, Truthahn, Deutschland, Vereinigtes Königreich, Italien, Portugal, Kanada, Australien, Argentinien, Frankreich, Niederlande, Polen
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