ID
38263
Beskrivning
Study ID: 111539 Clinical Study ID: 111539 Study Title: A Single-Blind Study of the Safety, Pharmacokinetics and Pharmacodynamics of scalating Repeat Doses of GSK249320 in Patients With Stroke Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00833989 https://clinicaltrials.gov/ct2/show/NCT00833989 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Refanezumab, Placebo Trade Name: N/A Study Indication: Ischaemic Attack, Transient The study consists of 8 visits: Day 1, Week 1 (Day 5), Week 2 (Day 10), Week 4 (Day 30), Week 8 (Day 60), Week 12 (Day 90), Week 16 (Day 112), Follow-up (F/U). All subjects will receive two doses. The first dose within 24-72 hrs after stroke the second dose 9 +/- 1 days after the first one. Each dose will be given as an intravenous infusion over 60 minutes. This document contains the concomitant medication form. It has to be filled in if concomitant medication has been taken by subject.
Länk
https://clinicaltrials.gov/ct2/show/NCT00833989
Nyckelord
Versioner (2)
- 2019-09-22 2019-09-22 -
- 2019-10-05 2019-10-05 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
5 oktober 2019
DOI
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Licens
Creative Commons BY-NC 3.0
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Safety, Pharmacokinetics and Pharmacodynamics of Refanezumab in Patients with Stroke, NCT00833989
Concomitant medication
- StudyEvent: ODM
Beskrivning
Concomitant Medication
Alias
- UMLS CUI-1
- C2347852
Beskrivning
Sequence Number
Datatyp
integer
Alias
- UMLS CUI [1]
- C2348184
Beskrivning
(Trade Name preferred)
Datatyp
text
Alias
- UMLS CUI [1,1]
- C2360065
- UMLS CUI [1,2]
- C2347852
Beskrivning
In the original form this item is hidden.
Datatyp
text
Alias
- UMLS CUI [1]
- C2826819
Beskrivning
Total daily dose
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C2347852
Beskrivning
Units of concomitant medication
Datatyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0439148
Beskrivning
Route of concomitant medication
Datatyp
text
Alias
- UMLS CUI [1]
- C2826730
Beskrivning
Reason for Medication
Datatyp
text
Alias
- UMLS CUI [1]
- C2826696
Beskrivning
day month year
Datatyp
partialDate
Alias
- UMLS CUI [1]
- C2826734
Beskrivning
Concomitant medication prior to study
Datatyp
text
Alias
- UMLS CUI [1]
- C2826667
Beskrivning
If you tick No, please specify End date in the following item.
Datatyp
text
Alias
- UMLS CUI [1]
- C2826666
Beskrivning
day month year
Datatyp
date
Alias
- UMLS CUI [1]
- C2826744
Similar models
Concomitant medication
- StudyEvent: ODM
C2347852 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,2])