ID

38589

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 information on repeated/unscheduled pharmacokinetic blood samples.

Link

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

Trefwoorden

  1. 25-10-19 25-10-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

25 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

Repeat Pharmacokinetics Blood

Administrative data
Beschrijving

Administrative data

Alias
UMLS CUI-1
C1320722
Subject Number
Beschrijving

Subject Number

Datatype

integer

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

Date/Time of Assessment

Datatype

datetime

Alias
UMLS CUI [1,1]
C2985720
UMLS CUI [1,2]
C1264639
Pharmacokinetics Blood - Unscheduled
Beschrijving

Pharmacokinetics Blood - Unscheduled

Alias
UMLS CUI-1
C0031328
UMLS CUI-2
C0005767
UMLS CUI-3
C3854240
Sample Number
Beschrijving

Sample Number

Datatype

integer

Alias
UMLS CUI [1]
C1299222
Date and time sample collected
Beschrijving

Date/time sample

Datatype

datetime

Alias
UMLS CUI [1,1]
C0200345
UMLS CUI [1,2]
C1264639
PK Sample ID
Beschrijving

PK Sample ID

Datatype

text

Alias
UMLS CUI [1,1]
C1299222
UMLS CUI [1,2]
C0201734

Similar models

Repeat Pharmacokinetics Blood

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])
Date/Time of Assessment
Item
Date/Time of Assessment
datetime
C2985720 (UMLS CUI [1,1])
C1264639 (UMLS CUI [1,2])
Item Group
Pharmacokinetics Blood - Unscheduled
C0031328 (UMLS CUI-1)
C0005767 (UMLS CUI-2)
C3854240 (UMLS CUI-3)
Sample Number
Item
Sample Number
integer
C1299222 (UMLS CUI [1])
Date/time sample
Item
Date and time sample collected
datetime
C0200345 (UMLS CUI [1,1])
C1264639 (UMLS CUI [1,2])
PK Sample ID
Item
PK Sample ID
text
C1299222 (UMLS CUI [1,1])
C0201734 (UMLS CUI [1,2])

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