ID
38598
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 Bronchoalveolar Lavage (BAL) and the samples collected during it; the BAL is performed for Cohort 7 only on Day 1, 5 hours after infusion start.
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
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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
Bronchoalveolar Lavage (BAL)
- StudyEvent: ODM
Description
Dosing Date and Time
Alias
- UMLS CUI-1
- C0178602
- UMLS CUI-2
- C1264639
Description
Bronchoalveolar Lavage
Alias
- UMLS CUI-1
- C1535502
Description
i.e. Start of BAL Procedure
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0200345
- UMLS CUI [1,2]
- C1264639
Description
BAL fluid aspirate 1 volume
Data type
float
Measurement units
- mL
Alias
- UMLS CUI [1,1]
- C0006279
- UMLS CUI [1,2]
- C0370199
- UMLS CUI [1,3]
- C0449468
Description
BAL fluid aspirate 2 volume
Data type
float
Measurement units
- mL
Alias
- UMLS CUI [1,1]
- C0006279
- UMLS CUI [1,2]
- C0370199
- UMLS CUI [1,3]
- C0449468
Description
BAL fluid aspirate 3 volume
Data type
float
Measurement units
- mL
Alias
- UMLS CUI [1,1]
- C0006279
- UMLS CUI [1,2]
- C0370199
- UMLS CUI [1,3]
- C0449468
Description
[hidden] Item is not required
Data type
datetime
Alias
- UMLS CUI [1,1]
- C1535502
- UMLS CUI [1,2]
- C1264639
Similar models
Bronchoalveolar Lavage (BAL)
- StudyEvent: ODM
C1264639 (UMLS CUI [1,2])
C3469597 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C1264639 (UMLS CUI [1,2])
C0370199 (UMLS CUI [1,2])
C0449468 (UMLS CUI [1,3])
C0370199 (UMLS CUI [1,2])
C0449468 (UMLS CUI [1,3])
C0370199 (UMLS CUI [1,2])
C0449468 (UMLS CUI [1,3])
C1264639 (UMLS CUI [1,2])
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