ID
38587
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 is to be filled in continously during the study and/or at the follow-up evaluation and contains information on other medication the participant has received during the course of the study.
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
Concomitant Medications
- StudyEvent: ODM
Description
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
Description
Concomitant Medication Number
Data type
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0600091
Description
Sequence Number
Data type
text
Alias
- UMLS CUI [1]
- C2348184
Description
Trade Name preferred
Data type
text
Alias
- UMLS CUI [1]
- C2360065
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1]
- C2826819
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0871468
Description
[hidden]
Data type
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1516698
- UMLS CUI [1,3]
- C0805701
Description
[hidden]
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0805701
- UMLS CUI [1,2]
- C0231175
Description
Concomitant Medication Unit Dose
Data type
text
Alias
- UMLS CUI [1]
- C2826811
Description
Concomitant Medication Units
Data type
text
Alias
- UMLS CUI [1]
- C2826646
Description
Concomitant Medication Frequency
Data type
text
Alias
- UMLS CUI [1]
- C2826654
Description
Concomitant Medication Route
Data type
text
Alias
- UMLS CUI [1]
- C2826730
Description
Concomitant Medication reason
Data type
text
Alias
- UMLS CUI [1]
- C2826696
Description
Concomitant Medication start date/time
Data type
partialDatetime
Alias
- UMLS CUI [1]
- C2826825
Description
Concomitant Medication Taken Prior to Study?
Data type
text
Alias
- UMLS CUI [1]
- C2826667
Description
If no, specify End Date and Time
Data type
text
Alias
- UMLS CUI [1]
- C2826666
Description
Concomitant Medication end date/time
Data type
partialDatetime
Alias
- UMLS CUI [1]
- C2826815
Similar models
Concomitant Medications
- StudyEvent: ODM
C1264639 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0231175 (UMLS CUI [1,2])
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