ID
38189
Descripción
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.
Link
https://clinicaltrials.gov/ct2/show/NCT00833989
Palabras clave
Versiones (1)
- 25/9/19 25/9/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
25 de septiembre de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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Safety, Pharmacokinetics and Pharmacodynamics of Refanezumab in Patients with Stroke, NCT00833989
Demography
- StudyEvent: ODM
Descripción
Demography
Alias
- UMLS CUI-1
- C1704791
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0421451
Descripción
If female, please record child-bearnig potential in the following item.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0079399
Descripción
Only in female patients.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3831118
Descripción
Ethnicity
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0015031
Descripción
Geographic ancestry
Alias
- UMLS CUI-1
- C3841890
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0085756
- UMLS CUI [3]
- C0027567
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1515945
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238696
- UMLS CUI [3]
- C1519427
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C4540996
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1556094
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238697
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C1513907
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0238604
- UMLS CUI [3]
- C2698217
Descripción
Check all that apply
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3841890
- UMLS CUI [2]
- C0043157
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Demography
- StudyEvent: ODM
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C0085756 (UMLS CUI [2])
C0027567 (UMLS CUI [3])
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C0238696 (UMLS CUI [2])
C1519427 (UMLS CUI [3])
C4540996 (UMLS CUI [2])
C1556094 (UMLS CUI [2])
C0238697 (UMLS CUI [2])
C1513907 (UMLS CUI [2])
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C2698217 (UMLS CUI [3])
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