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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