ID

38493

Beschrijving

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 basic information on the Holter ECG, which is scheduled at the Screening Visit and on Day 1, and which can also be performed as an additional (unscheduled/repeat) assessment.

Link

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

Trefwoorden

  1. 22-10-19 22-10-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

22 oktober 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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

  1. StudyEvent: ODM
    1. Holter
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Beschrijving

Subject Number

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Type of Visit
Beschrijving

Identical for all Parts/Cohorts/Subcohorts.

Datatype

integer

Alias
UMLS CUI [1]
C3641100
Date of Visit
Beschrijving

Date of Visit

Datatype

date

Alias
UMLS CUI [1]
C1320303
Holter
Beschrijving

Holter

Alias
UMLS CUI-1
C0013801
Measurement number
Beschrijving

only for repeat/unscheduled assessment

Datatype

integer

Alias
UMLS CUI [1,1]
C0013801
UMLS CUI [1,2]
C0449788
UMLS CUI [1,3]
C0242485
Dosing date/time
Beschrijving

[hidden] optional

Datatype

datetime

Alias
UMLS CUI [1,1]
C1264639
UMLS CUI [1,2]
C3469597
UMLS CUI [1,3]
C0304229
Start Date and Time of Holter
Beschrijving

Start Date/Time of Holter

Datatype

datetime

Alias
UMLS CUI [1,1]
C0013801
UMLS CUI [1,2]
C3897500
Stop Date and Time of Holter
Beschrijving

Stop Date/Time of Holter

Datatype

datetime

Alias
UMLS CUI [1,1]
C0013801
UMLS CUI [1,2]
C3899266
Interpretation of Holter
Beschrijving

If Abnormal - Clinically significant: 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

Datatype

integer

Alias
UMLS CUI [1,1]
C0013801
UMLS CUI [1,2]
C0438154

Similar models

  1. StudyEvent: ODM
    1. Holter
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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
Part A/B Day 1 (1 hour predose to 24 hours post start of infusion) (2)
CL Item
Repeat Assessment (3)
Date of Visit
Item
Date of Visit
date
C1320303 (UMLS CUI [1])
Item Group
Holter
C0013801 (UMLS CUI-1)
Holter measurement number
Item
Measurement number
integer
C0013801 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
C0242485 (UMLS CUI [1,3])
Dosing date/time
Item
Dosing date/time
datetime
C1264639 (UMLS CUI [1,1])
C3469597 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
Start Date/Time of Holter
Item
Start Date and Time of Holter
datetime
C0013801 (UMLS CUI [1,1])
C3897500 (UMLS CUI [1,2])
Stop Date/Time of Holter
Item
Stop Date and Time of Holter
datetime
C0013801 (UMLS CUI [1,1])
C3899266 (UMLS CUI [1,2])
Item
Interpretation of Holter
integer
C0013801 (UMLS CUI [1,1])
C0438154 (UMLS CUI [1,2])
Code List
Interpretation of Holter
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
CL Item
No result (optional item) (4)
CL Item
Unable to evaluate (optional item) (5)

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