ID

38903

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 Spirometry which is performed at Screening, on Days 1, 2 and 28, in case of early withdrawal and as an unscheduled (repeat) assessment.

Link

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

Keywords

  1. 10/22/19 10/22/19 -
  2. 11/12/19 11/12/19 - Sarah Riepenhausen
Copyright Holder

GlaxoSmithKline

Uploaded on

November 12, 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

Spirometry

  1. StudyEvent: ODM
    1. Spirometry
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Description

Subject Number

Data type

integer

Alias
UMLS CUI [1]
C2348585
Type of Visit
Description

Identical for all Parts/Cohorts/Subcohorts. The Visit on Day 28 is denoted as "Follow-Up" for Part A but not for Part B.

Data type

integer

Alias
UMLS CUI [1]
C3641100
Date of Visit
Description

Date of Visit

Data type

date

Alias
UMLS CUI [1]
C1320303
Dosing Date and Time
Description

Dosing Date and Time

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

only applicable to Day 1 Visits

Data type

datetime

Alias
UMLS CUI [1,1]
C3897500
UMLS CUI [1,2]
C3469597
UMLS CUI [1,3]
C0304229
Spirometry
Description

Spirometry

Alias
UMLS CUI-1
C0037981
Time relative to dosing
Description

Applicable to Day 1 only. All cohorts have to perform the predose measurement, subjects of cohort 7 additionally the 7 hours post start of infusion measurement and all other cohorts the 6 hours post start of infusion measurement.

Data type

integer

Alias
UMLS CUI [1,1]
C0439564
UMLS CUI [1,2]
C3469597
UMLS CUI [1,3]
C0304229
Measurement Number
Description

for Repeat / Unscheduled assessments

Data type

integer

Alias
UMLS CUI [1,1]
C0037981
UMLS CUI [1,2]
C0449788
UMLS CUI [1,3]
C0242485
Date/time of test (Start of Assessment)
Description

Spirometry Date/Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0037981
UMLS CUI [1,2]
C1264639
FEV1 (Best of 3)
Description

FEV1

Data type

float

Measurement units
  • L
Alias
UMLS CUI [1]
C0748133
L
FVC (Best of 3)
Description

FVC

Data type

float

Measurement units
  • L
Alias
UMLS CUI [1]
C1287681
L

Similar models

Spirometry

  1. StudyEvent: ODM
    1. Spirometry
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])
Item
Type of Visit
integer
C3641100 (UMLS CUI [1])
Code List
Type of Visit
CL Item
Screening (1)
CL Item
Early Withdrawal (2)
CL Item
Part A/B, Day 1 (3)
CL Item
Part A/B, Day 2 (4)
CL Item
Part A/B, Day 28 (5)
CL Item
Repeat Assessment (6)
Date of Visit
Item
Date of Visit
date
C1320303 (UMLS CUI [1])
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
Spirometry
C0037981 (UMLS CUI-1)
Item
Time relative to dosing
integer
C0439564 (UMLS CUI [1,1])
C3469597 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
Code List
Time relative to dosing
CL Item
Predose (1)
CL Item
6 Hours Post Start of Infusion (2)
CL Item
7 Hours Post Start of Infusion (3)
Repeat Spirometry Measurement Number
Item
Measurement Number
integer
C0037981 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
C0242485 (UMLS CUI [1,3])
Spirometry Date/Time
Item
Date/time of test (Start of Assessment)
datetime
C0037981 (UMLS CUI [1,1])
C1264639 (UMLS CUI [1,2])
FEV1
Item
FEV1 (Best of 3)
float
C0748133 (UMLS CUI [1])
FVC
Item
FVC (Best of 3)
float
C1287681 (UMLS CUI [1])

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