0 Ratings

ID

38597

Description

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 the telemetry assessment which is performed on Day 1 one hour pre-dose to 12 hours post start of infusion (for all cohorts/Parts).

Link

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

Keywords

  1. 10/25/19 10/25/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

October 25, 2019

DOI

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License

Creative Commons BY-NC 3.0

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

    Telemetry

    1. StudyEvent: ODM
      1. Telemetry
    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Number
    Description

    Subject Number

    Data type

    integer

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

    Date/Time of Assessment

    Data type

    datetime

    Alias
    UMLS CUI [1,1]
    C2985720
    UMLS CUI [1,2]
    C1264639
    Dosing Date and Time
    Description

    Dosing Date and Time

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

    Read-only

    Data type

    datetime

    Alias
    UMLS CUI [1,1]
    C3897500
    UMLS CUI [1,2]
    C3469597
    UMLS CUI [1,3]
    C0304229
    Telemetry 1 Hour Predose To 12 Hours Post Start of Infusion
    Description

    Telemetry 1 Hour Predose To 12 Hours Post Start of Infusion

    Alias
    UMLS CUI-1
    C0039451
    UMLS CUI-2
    C1948053
    Start Date and Time
    Description

    Telemetry Start Date/Time

    Data type

    datetime

    Alias
    UMLS CUI [1,1]
    C3897500
    UMLS CUI [1,2]
    C0039451
    Stop Date and Time
    Description

    Telemetry Stop Date/Time

    Data type

    datetime

    Alias
    UMLS CUI [1,1]
    C0039451
    UMLS CUI [1,2]
    C3899266
    Result of Telemetry
    Description

    Complete the abnormality form for all clinically significant abnormalities, and additionally complete the AE form if the abnormality meets the protocol definition for an AE

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0039451
    UMLS CUI [1,2]
    C0456984

    Similar models

    Telemetry

    1. StudyEvent: ODM
      1. Telemetry
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    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 and Time
    C0178602 (UMLS CUI-1)
    C1264639 (UMLS CUI-2)
    Start Dosing date/time
    Item
    Start Dosing date/time
    datetime
    C3897500 (UMLS CUI [1,1])
    C3469597 (UMLS CUI [1,2])
    C0304229 (UMLS CUI [1,3])
    Item Group
    Telemetry 1 Hour Predose To 12 Hours Post Start of Infusion
    C0039451 (UMLS CUI-1)
    C1948053 (UMLS CUI-2)
    Telemetry Start Date/Time
    Item
    Start Date and Time
    datetime
    C3897500 (UMLS CUI [1,1])
    C0039451 (UMLS CUI [1,2])
    Telemetry Stop Date/Time
    Item
    Stop Date and Time
    datetime
    C0039451 (UMLS CUI [1,1])
    C3899266 (UMLS CUI [1,2])
    Item
    Result of Telemetry
    integer
    C0039451 (UMLS CUI [1,1])
    C0456984 (UMLS CUI [1,2])
    Code List
    Result of Telemetry
    CL Item
    Normal (1)
    CL Item
    Abnormal - Not clinically significant (2)
    CL Item
    Abnormal - Clinically significant (3)

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