- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01230801
Safety/Tolerability/Pharmacokinetic (PK)/Pharmacodynamics (PD) Study of BMN701 in Patients With Late-Onset Pompe Disease
8. mai 2018 oppdatert av: BioMarin Pharmaceutical
A Phase 1/2 Open-label Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamic and Preliminary Efficacy of BMN 701 (GILT-tagged Recombinant Human GAA) in Patients With Late-onset Pompe Disease
A Phase 1/2, open-label, multicenter, multiple dose escalation study of BMN 701 administered by intravenous infusion every 2 weeks over a 24-week treatment period to patients with late-onset Pompe disease.
Studieoversikt
Studietype
Intervensjonell
Registrering (Faktiske)
22
Fase
- Fase 2
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Adelaide, SA
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Adelaide, Adelaide, SA, Australia, 5006
- Royal Adelaide Hospital, SA Pathology
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California
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La Jolla, California, Forente stater, 92103-8765
- Univ of California San Diego School of Medicine
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Florida
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Gainesville, Florida, Forente stater, 32610
- University of Florida College of Medicine
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Kansas
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Kansas City, Kansas, Forente stater, 66160
- University of Kansas Medical Center
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-
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-
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Nice, Frankrike, 06202
- Hôpital de I´Archet- Centre Hospitalier Universitaire Nice
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Paris Cedex 13, Frankrike, 75651
- Hôpital Pitié-Salpêtrière
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Birmingham, Storbritannia, B15 2TH
- Old Queen Elizabeth Hospital, Department of Medicine
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London, Storbritannia, NW3 2QG
- Royal Free Hospital
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Salford, Storbritannia, M6 8HD
- Salford Royal Hospital NHS Trust
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Rheinland-pfalz
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Mainz, Rheinland-pfalz, Tyskland, 55131
- Zentrum für Kinder- und Jugenmedizin
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
13 år og eldre (Barn, Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion criteria:
- Patient has been diagnosed with Pompe Disease prior to or during the screening period based on 2 GAA gene mutations and either: endogenous GAA activity <75% of the lower limit of the normal adult range reported by the testing laboratory, as assessed in cultured skin fibroblasts -or- endogenous GAA activity <75% of the lower limit of the normal adult range reported by the testing laboratory, as assessed by dried blood spot or whole blood assay;
- Patient is male or female and 13 years of age or older at the time of enrollment in the study;
- Sexually active patients must be willing to use an acceptable method of contraception while participating in the study and for at least 4 months following the last dose of BMN 701;
- If patient is female and not considered to be of childbearing potential, she is at least 2 years post-menopausal or had tubal ligation at least 1 year prior to screening, or who have had total hysterectomy;
- If patient is female and of childbearing potential, she has negative urine pregnancy tests during the Screening Period and at the Baseline visit and be willing to have additional pregnancy tests during the study;
- Patient has ≥30% predicted upright FVC and either <80% predicted upright FVC, or >10% reduction in supine FVC compared to upright FVC during the Screening Period;
- Patient is naïve to Enzyme Replacement Therapy (ERT) with rhGAA;
- Patient must be able to ambulate at least 40 meters (131.2 feet) on the 6MWT conducted at the Screening visit (use of assistive devices such as walker, cane, or crutches, is permitted); and
- If subject was female, she was not lactating
Exclusion criteria:
- Patient has a history of diabetes or other disease known to cause hypoglycemia and is currently receiving, or might anticipate receiving, hypoglycemic agents during the course of the study;
- Patient has been on any immunosuppressive medication other than glucocorticosteroids within 1 year prior to enrollment into this study;
- Patient requires invasive ventilatory assistance at the time of enrollment into the study;
- Patient has received any investigational medication within 30 days prior to the first dose of study drug or is scheduled to receive any investigational drug other than BMN 701 during the course of the study;
- Patient has previously been admitted to the study;
- Patient is breastfeeding at screening or planning to become pregnant (self or partner) at any time during the study;
- Patient has a medical condition or extenuating circumstance that, in the opinion of the Investigator, might compromise the patient's ability to comply with the protocol requirements or compromise the patient's well being or safety;
- Patient has any condition that, in the view of the Investigator, places the patient at high risk of poor treatment compliance or of not completing the study.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: BMN 701
IV infusion
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GILT-merket rekombinant human GAA
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Number of Participants With Adverse Events
Tidsramme: 24 weeks
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Number of Participants with Adverse Events as a Measure of Safety and Tolerability
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24 weeks
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change From Baseline in Six Minutes Walk Test
Tidsramme: Baseline up to 24 weeks
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Change from Baseline in Six Minutes Walk Test.
The 6MWT measured the maximum distance the subject could walk on a flat, hard surface in a period of 6 minutes
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Baseline up to 24 weeks
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Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change From Baseline in Percent Predicted Upright Forced Vital Capacity
Tidsramme: Baseline up to 24 week
|
Change from Baseline in Percent Predicted Upright Forced Vital Capacity.
Changes in respiratory function were assessed by measurement of MEP, MIP and MVV; and percent predicted upright and supine FVC.
|
Baseline up to 24 week
|
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Change From Baseline in Percent Predicted Supine Forced Vital Capacity
Tidsramme: Baseline up to 24 weeks
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Change from Baseline in Percent Predicted Supine Forced Vital Capacity.
Changes in respiratory function were assessed by measurement of MEP, MIP and MVV; and percent predicted upright and supine FVC.
|
Baseline up to 24 weeks
|
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Change From Baseline in Percent Predicted Upright Maximum Expiratory Pressure
Tidsramme: Baseline up to 24 weeks
|
Change from Baseline in Percent Predicted Upright Maximum Expiratory Pressure.
Changes in respiratory function were assessed by measurement of MEP, MIP and MVV; and percent predicted upright and supine FVC.
|
Baseline up to 24 weeks
|
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Change From Baseline in Percent Predicted Upright Maximum Inspiratory Pressure
Tidsramme: Baseline up to 24 weeks
|
Change from Baseline in Percent Predicted Upright Maximum Inspiratory Pressure.
Changes in respiratory function were assessed by measurement of MEP, MIP and MVV; and percent predicted upright and supine FVC.
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Baseline up to 24 weeks
|
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Change From Baseline in Upright Maximum Ventilatory Volume
Tidsramme: Baseline up to 24 weeks
|
Change from Baseline in Upright Maximum Ventilatory Volume.
Changes in respiratory function were assessed by measurement of MEP, MIP and MVV; and percent predicted upright and supine FVC.
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Baseline up to 24 weeks
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Studieleder: Medical Monitor, BioMarin Pharmaceutical
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
17. januar 2011
Primær fullføring (Faktiske)
6. mars 2013
Studiet fullført (Faktiske)
6. mars 2013
Datoer for studieregistrering
Først innsendt
27. oktober 2010
Først innsendt som oppfylte QC-kriteriene
28. oktober 2010
Først lagt ut (Anslag)
29. oktober 2010
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
11. juni 2018
Siste oppdatering sendt inn som oppfylte QC-kriteriene
8. mai 2018
Sist bekreftet
1. mai 2018
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Metabolske sykdommer
- Hjernesykdommer
- Sykdommer i sentralnervesystemet
- Sykdommer i nervesystemet
- Genetiske sykdommer, medfødte
- Karbohydratmetabolisme, medfødte feil
- Metabolisme, medfødte feil
- Lysosomale lagringssykdommer
- Hjernesykdommer, metabolske
- Hjernesykdommer, metabolske, medfødte
- Lysosomale lagringssykdommer, nervesystemet
- Glykogenlagringssykdom
- Glykogenlagringssykdom Type II
Andre studie-ID-numre
- POM-001
- 2010-023561-22 (EudraCT-nummer)
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Ja
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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