ID

38592

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 urine samples for pharmacokinetics which are collected on Days 1 and 2.

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 Urine

  1. StudyEvent: ODM
    1. Pharmacokinetics Urine
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

Datentyp

datetime

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C1264639
Pharmacokinetics Urine
Beschreibung

Pharmacokinetics Urine

Alias
UMLS CUI-1
C0031328
UMLS CUI-2
C0042036
Urine Collection Period
Beschreibung

Fill in entire repeating itemgroup for each period

Datentyp

integer

Alias
UMLS CUI [1,1]
C0200354
UMLS CUI [1,2]
C1948053
Was all of the sample collected for this interval?
Beschreibung

Not applicable to predose collection period

Datentyp

text

Alias
UMLS CUI [1,1]
C0200354
UMLS CUI [1,2]
C0205197
Start date and Actual start time
Beschreibung

Start date/time urine collection

Datentyp

datetime

Alias
UMLS CUI [1,1]
C0200354
UMLS CUI [1,2]
C3897500
Stop date and Actual stop time
Beschreibung

Not applicable to predose collection period

Datentyp

datetime

Alias
UMLS CUI [1,1]
C0200354
UMLS CUI [1,2]
C3899266
Total sample volume
Beschreibung

Urine sample volume

Datentyp

float

Maßeinheiten
  • mL
Alias
UMLS CUI [1]
C1278293
mL

Ähnliche Modelle

Pharmacokinetics Urine

  1. StudyEvent: ODM
    1. Pharmacokinetics Urine
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])
C0304229 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
Item Group
Pharmacokinetics Urine
C0031328 (UMLS CUI-1)
C0042036 (UMLS CUI-2)
Item
Urine Collection Period
integer
C0200354 (UMLS CUI [1,1])
C1948053 (UMLS CUI [1,2])
Code List
Urine Collection Period
CL Item
Day 1 Predose (1)
CL Item
0-8 Hours Post Start of Infusion (2)
CL Item
8-16 Hours Post Start of Infusion (3)
CL Item
16-24 Hours Post Start of Infusion (4)
CL Item
24-32 Hours Post Start of Infusion (5)
CL Item
32-40 Hours Post Start of Infusion (6)
CL Item
40-48 Hours Post Start of Infusion (7)
Item
Was all of the sample collected for this interval?
text
C0200354 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
Code List
Was all of the sample collected for this interval?
CL Item
Yes (Y)
CL Item
No (N)
Start date/time urine collection
Item
Start date and Actual start time
datetime
C0200354 (UMLS CUI [1,1])
C3897500 (UMLS CUI [1,2])
Stop date/time urine collection
Item
Stop date and Actual stop time
datetime
C0200354 (UMLS CUI [1,1])
C3899266 (UMLS CUI [1,2])
Urine sample volume
Item
Total sample volume
float
C1278293 (UMLS CUI [1])

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