ID
38587
Beschreibung
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
Stichworte
Versionen (1)
- 25.10.19 25.10.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
25. Oktober 2019
DOI
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Lizenz
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
Beschreibung
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
Beschreibung
Concomitant Medication Number
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0600091
Beschreibung
Sequence Number
Datentyp
text
Alias
- UMLS CUI [1]
- C2348184
Beschreibung
Trade Name preferred
Datentyp
text
Alias
- UMLS CUI [1]
- C2360065
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C2826819
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0871468
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1516698
- UMLS CUI [1,3]
- C0805701
Beschreibung
[hidden]
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0805701
- UMLS CUI [1,2]
- C0231175
Beschreibung
Concomitant Medication Unit Dose
Datentyp
text
Alias
- UMLS CUI [1]
- C2826811
Beschreibung
Concomitant Medication Units
Datentyp
text
Alias
- UMLS CUI [1]
- C2826646
Beschreibung
Concomitant Medication Frequency
Datentyp
text
Alias
- UMLS CUI [1]
- C2826654
Beschreibung
Concomitant Medication Route
Datentyp
text
Alias
- UMLS CUI [1]
- C2826730
Beschreibung
Concomitant Medication reason
Datentyp
text
Alias
- UMLS CUI [1]
- C2826696
Beschreibung
Concomitant Medication start date/time
Datentyp
partialDatetime
Alias
- UMLS CUI [1]
- C2826825
Beschreibung
Concomitant Medication Taken Prior to Study?
Datentyp
text
Alias
- UMLS CUI [1]
- C2826667
Beschreibung
If no, specify End Date and Time
Datentyp
text
Alias
- UMLS CUI [1]
- C2826666
Beschreibung
Concomitant Medication end date/time
Datentyp
partialDatetime
Alias
- UMLS CUI [1]
- C2826815
Ähnliche Modelle
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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