ID
38595
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 Randomisation of trial participants as well as the actual application of the investigational product GSK1995057 on Day 1.
Link
https://clinicaltrials.gov/ct2/show/NCT01476046
Keywords
Versions (1)
- 10/25/19 10/25/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
October 25, 2019
DOI
To request one please log in.
License
Creative Commons BY-NC 3.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
Phase I Trial of Intravenous TNFR1 Antagonist GSK1995057 in Healthy Subjects - NCT01476046
Randomisation and Investigational Product - IV Dosing
- StudyEvent: ODM
Description
Randomisation Number
Alias
- UMLS CUI-1
- C0034656
- UMLS CUI-2
- C0237753
Description
If yes, provide Randomisation Number and Date/time of randomisation
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0332149
Description
if applicable
Data type
integer
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0237753
Description
if applicable
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C1264639
Description
Investigational Product - IV dosing
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0678766
- UMLS CUI-3
- C0348016
Description
Time is optional
Data type
partialDatetime
Alias
- UMLS CUI [1,1]
- C3897500
- UMLS CUI [1,2]
- C3469597
- UMLS CUI [1,3]
- C0304229
Description
Time is optional
Data type
partialDatetime
Alias
- UMLS CUI [1,1]
- C3899266
- UMLS CUI [1,2]
- C3469597
- UMLS CUI [1,3]
- C0304229
Description
Dose of investigational product
Data type
float
Measurement units
- mg
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0678766
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0678766
- UMLS CUI [1,3]
- C1519795
Description
If no, record reasons. Per Protocol treatment: 0.0004 mg/kg (Cohort 1), 0.002 mg/kg (Cohort 2), 0.01 mg/kg (Cohort 3), 0.05 mg/kg (Cohort 4), 0.25 mg/kg (Cohort 5), 2.0 mg/kg (Cohort 6/7), administered over 1 hour (Cohort 1), 2 hours (Cohort 2) or 3 hours (Cohorts 3 to 7).
Data type
text
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C2349182
Description
if applicable
Data type
text
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C3827420
Similar models
Randomisation and Investigational Product - IV Dosing
- StudyEvent: ODM
C1264639 (UMLS CUI [1,2])
C0332149 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,2])
C0678766 (UMLS CUI-2)
C0348016 (UMLS CUI-3)
C3469597 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C3469597 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C0678766 (UMLS CUI [1,2])
C0678766 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
C2349182 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C3827420 (UMLS CUI [1,3])