ID
38597
Descrizione
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).
collegamento
https://clinicaltrials.gov/ct2/show/NCT01476046
Keywords
versioni (1)
- 25/10/19 25/10/19 -
Titolare del copyright
GlaxoSmithKline
Caricato su
25 ottobre 2019
DOI
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Licenza
Creative Commons BY-NC 3.0
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Phase I Trial of Intravenous TNFR1 Antagonist GSK1995057 in Healthy Subjects - NCT01476046
Telemetry
- StudyEvent: ODM
Descrizione
Dosing Date and Time
Alias
- UMLS CUI-1
- C0178602
- UMLS CUI-2
- C1264639
Descrizione
Telemetry 1 Hour Predose To 12 Hours Post Start of Infusion
Alias
- UMLS CUI-1
- C0039451
- UMLS CUI-2
- C1948053
Descrizione
Telemetry Start Date/Time
Tipo di dati
datetime
Alias
- UMLS CUI [1,1]
- C3897500
- UMLS CUI [1,2]
- C0039451
Descrizione
Telemetry Stop Date/Time
Tipo di dati
datetime
Alias
- UMLS CUI [1,1]
- C0039451
- UMLS CUI [1,2]
- C3899266
Descrizione
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
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0039451
- UMLS CUI [1,2]
- C0456984
Similar models
Telemetry
- StudyEvent: ODM
C1264639 (UMLS CUI [1,2])
C3469597 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C1948053 (UMLS CUI-2)
C0039451 (UMLS CUI [1,2])
C3899266 (UMLS CUI [1,2])
C0456984 (UMLS CUI [1,2])
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