ID

38591

Beskrivning

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.

Länk

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

Nyckelord

  1. 2019-10-25 2019-10-25 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

25 oktober 2019

DOI

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Licens

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
Beskrivning

Administrative data

Alias
UMLS CUI-1
C1320722
Subject Number
Beskrivning

Subject Number

Datatyp

integer

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

Date/Time of Assessment

Datatyp

datetime

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

Dosing date/time

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

Optional and read-only only relevant for Day 1 Samples

Datatyp

datetime

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

Pharmacokinetics

Alias
UMLS CUI-1
C0031328
Scheduled Time of Sample
Beskrivning

Fill in entire repeating itemgroup for each time points

Datatyp

integer

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

For up to 9 hours after infusion start

Datatyp

time

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

For 12/24/48 hours post infusion start

Datatyp

date

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

Similar models

Pharmacokinetics

  1. StudyEvent: ODM
    1. Pharmacokinetics
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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