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ID

38591

Beschreibung

Study ID: 110951 Clinical Study ID: 110951 Study Title: A two-part, randomised, placebo-controlled study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of single doses of intravenously infused GSK1995057 in healthy subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01476046 See https://clinicaltrials.gov/ct2/show/NCT01476046 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: N/A, Placebo Trade Name: N/A Study Indication: Respiratory Disorders This phase I trial primarily studies the safety and tolerability of ascending single intravenous doses of the selective TNFR1 antagonist GSK1995057 in healthy volunteers, and secondly explores the drug's pharmacodynamics, pharmacokinetics, concentration in lung epithelial lining fluid as well as its effect on immune system markers. The drug is hypothesized to be useful for Acute Lung Injury. The single-centre study consists of two parts A and B with seven cohorts/ten subcohorts in total. Part A includes ascending doses of the investigational product given to subjects negative or positive for pre-existing human anti-heavy chain variable domain (HAVH) antibodies (Cohorts 1 to 3 with Subcohorts 1a, 2a and 3a negative for HAVH and 1b, 2b, 3b positive for HAVH). Part B includes only subjects negative for HAVH, with ascending doses given to Cohorts 4 to 6. Cohort 7 receives the same dose as Cohort 6, but whereas the other Cohorts are single-blinded, Cohort 7 is open-label and additionally receives a bronchoalveolar lavage (BAL). The study consists of a Screening Visit (up to 56 days before Day 1, the day of the drug administration), Visits on Day -1, 1, 2, 3, 5, 7, 14, 28 and Follow-Up Visits on Day 57 and 85. This form contains information on pharmacokinetic samples which are taken repeatedly on Day 1, 2 and 3.

Link

https://clinicaltrials.gov/ct2/show/NCT01476046

Stichworte

  1. 25.10.19 25.10.19 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

25. Oktober 2019

DOI

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Lizenz

Creative Commons BY-NC 3.0

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    Phase I Trial of Intravenous TNFR1 Antagonist GSK1995057 in Healthy Subjects - NCT01476046

    Pharmacokinetics

    1. StudyEvent: ODM
      1. Pharmacokinetics
    Administrative data
    Beschreibung

    Administrative data

    Alias
    UMLS CUI-1
    C1320722
    Subject Number
    Beschreibung

    Subject Number

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Date/Time of Assessment
    Beschreibung

    Date/Time of Assessment

    Datentyp

    datetime

    Alias
    UMLS CUI [1,1]
    C2985720
    UMLS CUI [1,2]
    C1264639
    Dosing date/time
    Beschreibung

    Dosing date/time

    Alias
    UMLS CUI-1
    C0178602
    UMLS CUI-2
    C1264639
    Dosing date/time
    Beschreibung

    Optional and read-only only relevant for Day 1 Samples

    Datentyp

    datetime

    Alias
    UMLS CUI [1,1]
    C0178602
    UMLS CUI [1,2]
    C1264639
    Pharmacokinetics
    Beschreibung

    Pharmacokinetics

    Alias
    UMLS CUI-1
    C0031328
    Scheduled Time of Sample
    Beschreibung

    Fill in entire repeating itemgroup for each time points

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0040223
    UMLS CUI [1,2]
    C0200345
    UMLS CUI [1,3]
    C1301732
    Actual Time of Sample
    Beschreibung

    For up to 9 hours after infusion start

    Datentyp

    time

    Alias
    UMLS CUI [1,1]
    C0040223
    UMLS CUI [1,2]
    C0200345
    Actual Date/Time of Sample
    Beschreibung

    For 12/24/48 hours post infusion start

    Datentyp

    date

    Alias
    UMLS CUI [1,1]
    C1264639
    UMLS CUI [1,2]
    C0200345

    Ähnliche Modelle

    Pharmacokinetics

    1. StudyEvent: ODM
      1. Pharmacokinetics
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Administrative data
    C1320722 (UMLS CUI-1)
    Subject Number
    Item
    Subject Number
    integer
    C2348585 (UMLS CUI [1])
    Date/Time of Assessment
    Item
    Date/Time of Assessment
    datetime
    C2985720 (UMLS CUI [1,1])
    C1264639 (UMLS CUI [1,2])
    Item Group
    Dosing date/time
    C0178602 (UMLS CUI-1)
    C1264639 (UMLS CUI-2)
    Dosing date/time
    Item
    Dosing date/time
    datetime
    C0178602 (UMLS CUI [1,1])
    C1264639 (UMLS CUI [1,2])
    Item Group
    Pharmacokinetics
    C0031328 (UMLS CUI-1)
    Item
    Scheduled Time of Sample
    integer
    C0040223 (UMLS CUI [1,1])
    C0200345 (UMLS CUI [1,2])
    C1301732 (UMLS CUI [1,3])
    Code List
    Scheduled Time of Sample
    CL Item
    Part A/B Day 1 Predose (1)
    CL Item
    Part A/B Day 1 0.5 Hours Post Start of Infusion (2)
    CL Item
    Part A/B Day 1 1 Hour Post Start of Infusion (3)
    CL Item
    Part A/B Day 1 2 Hours Post Start of Infusion (4)
    CL Item
    Part A/B Day 1 3 Hours Post Start of Infusion (5)
    CL Item
    Part A/B Day 1 4 Hours Post Start of Infusion (6)
    CL Item
    Part A/B Day 1 6 Hours Post Start of Infusion (7)
    CL Item
    Part A/B Day 1 9 Hours Post Start of Infusion (8)
    CL Item
    Part A/B Day 1 12 Hours Post Start of Infusion (9)
    CL Item
    Part A/B Day 2 24 Hours Post Start of Infusion (10)
    CL Item
    Part A/B Day 3 48 Hours Post Start of Infusion (11)
    Time of Sample
    Item
    Actual Time of Sample
    time
    C0040223 (UMLS CUI [1,1])
    C0200345 (UMLS CUI [1,2])
    Date/Time of Sample
    Item
    Actual Date/Time of Sample
    date
    C1264639 (UMLS CUI [1,1])
    C0200345 (UMLS CUI [1,2])

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