ID
38587
Beskrivning
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.
Länk
https://clinicaltrials.gov/ct2/show/NCT01476046
Nyckelord
Versioner (1)
- 2019-10-25 2019-10-25 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
25 oktober 2019
DOI
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Licens
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
Beskrivning
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
Beskrivning
Concomitant Medication Number
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0600091
Beskrivning
Sequence Number
Datatyp
text
Alias
- UMLS CUI [1]
- C2348184
Beskrivning
Trade Name preferred
Datatyp
text
Alias
- UMLS CUI [1]
- C2360065
Beskrivning
[hidden]
Datatyp
text
Alias
- UMLS CUI [1]
- C2826819
Beskrivning
[hidden]
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0871468
Beskrivning
[hidden]
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1516698
- UMLS CUI [1,3]
- C0805701
Beskrivning
[hidden]
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0805701
- UMLS CUI [1,2]
- C0231175
Beskrivning
Concomitant Medication Unit Dose
Datatyp
text
Alias
- UMLS CUI [1]
- C2826811
Beskrivning
Concomitant Medication Units
Datatyp
text
Alias
- UMLS CUI [1]
- C2826646
Beskrivning
Concomitant Medication Frequency
Datatyp
text
Alias
- UMLS CUI [1]
- C2826654
Beskrivning
Concomitant Medication Route
Datatyp
text
Alias
- UMLS CUI [1]
- C2826730
Beskrivning
Concomitant Medication reason
Datatyp
text
Alias
- UMLS CUI [1]
- C2826696
Beskrivning
Concomitant Medication start date/time
Datatyp
partialDatetime
Alias
- UMLS CUI [1]
- C2826825
Beskrivning
Concomitant Medication Taken Prior to Study?
Datatyp
text
Alias
- UMLS CUI [1]
- C2826667
Beskrivning
If no, specify End Date and Time
Datatyp
text
Alias
- UMLS CUI [1]
- C2826666
Beskrivning
Concomitant Medication end date/time
Datatyp
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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