ID
38189
Description
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 demography form. It has to be filled in for Day 1.
Lien
https://clinicaltrials.gov/ct2/show/NCT00833989
Mots-clés
Versions (1)
- 25/09/2019 25/09/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
25 septembre 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Safety, Pharmacokinetics and Pharmacodynamics of Refanezumab in Patients with Stroke, NCT00833989
Demography
- StudyEvent: ODM
Description
Demography
Alias
- UMLS CUI-1
- C1704791
Description
day month year
Type de données
date
Alias
- UMLS CUI [1]
- C0421451
Description
If female, please record child-bearnig potential in the following item.
Type de données
text
Alias
- UMLS CUI [1]
- C0079399
Description
Only in female patients.
Type de données
integer
Alias
- UMLS CUI [1]
- C3831118
Description
Ethnicity
Type de données
integer
Alias
- UMLS CUI [1]
- C0015031
Description
Geographic ancestry
Alias
- UMLS CUI-1
- C3841890
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0085756
- UMLS CUI [3]
- C0027567
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1515945
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238696
- UMLS CUI [3]
- C1519427
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C4540996
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1556094
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238697
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1513907
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238604
- UMLS CUI [3]
- C2698217
Description
Check all that apply
Type de données
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0043157
Similar models
Demography
- StudyEvent: ODM
C2986440 (UMLS CUI [1,2])
C0085756 (UMLS CUI [2])
C0027567 (UMLS CUI [3])
C1515945 (UMLS CUI [2])
C0238696 (UMLS CUI [2])
C1519427 (UMLS CUI [3])
C4540996 (UMLS CUI [2])
C1556094 (UMLS CUI [2])
C0238697 (UMLS CUI [2])
C1513907 (UMLS CUI [2])
C0238604 (UMLS CUI [2])
C2698217 (UMLS CUI [3])
C0043157 (UMLS CUI [2])