ID
39859
Descripción
Study ID: 110399 Clinical Study ID: 110399 Study Title: A randomized, double blind, parallel group, placebo controlled 28 day study to investigate the safety, tolerability and pharmacodynamics of SB-656933 in subjects with cystic fibrosis. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00903201 https://clinicaltrials.gov/ct2/show/NCT00903201?term=NCT00903201 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: SB656933, Placebo Trade Name: N/A Study Indication: Cystic Fibrosis The study consists of a screening, five study visits and a follow-up (time relative to Baseline in days): Visit 1: Screening, Day -28 to -16 Visit 2a: Day -7 to -4 Visit 2b: Day 1 Visit 3: Day 14 Visit 4: Day 21 Visit 5: Day 28 Visit 6: Early Withdrawal/ Follow-up, Day 35 to 42. From day 1 to day 28 the patients will receive daily doses. This document contains the Status of treatment Blind, the Study conclusion and the Pregnancy information form. It has to be filled in for follow-up.
Link
https://clinicaltrials.gov/ct2/show/NCT00903201?term=NCT00903201
Palabras clave
Versiones (2)
- 19/2/20 19/2/20 -
- 24/2/20 24/2/20 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
24 de febrero de 2020
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 4.0
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Safety, tolerability and pharmacodynamics of Elubrixin in cystic fibrosis patients, NCT00903201
Treatment Blind, Study conclusion, Pregnancy information
- StudyEvent: ODM
Descripción
Status of treatment Blind
Alias
- UMLS CUI-1
- C0749659
- UMLS CUI-2
- C2347038
Descripción
If you tick yes, please fill in the following items, complete the Adverse Event form and/or Investigational Product forms as appropriate.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3897431
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
Descripción
00:00-23:59
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0040223
Descripción
Reason blind broken
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
Descripción
Other Reason blind broken
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0205394
Descripción
Study conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0805839
Descripción
If you tick yes, please complete details in the following items.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0422727
Descripción
day month year
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0679006
- UMLS CUI [1,3]
- C0011008
Descripción
If you tick "Adverse event", record details on the Non-Serious Adverse Events or Serious Adverse Events forms as appropriate. Select "Investigator discretion" if none of the other primary reasons are appropriate.
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Descripción
Reason for withdrawal, Investigator discretion, specification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0008961
- UMLS CUI [1,2]
- C0022423
- UMLS CUI [1,3]
- C2349954
- UMLS CUI [1,4]
- C0566251
Descripción
Data owner should check the box when data cleaning is complete.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1706256
- UMLS CUI [1,2]
- C1519316
Descripción
Office Use 1
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0008976
- UMLS CUI [1,2]
- C1707478
- UMLS CUI [1,3]
- C0442603
- UMLS CUI [1,4]
- C1524063
Descripción
Office Use 2
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0008976
- UMLS CUI [1,2]
- C1707478
- UMLS CUI [1,3]
- C0442603
- UMLS CUI [1,4]
- C1524063
Descripción
Pregnancy information (female)
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
- UMLS CUI-3
- C0086287
Descripción
Pregnancy information (male)
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
- UMLS CUI-3
- C0086582
Similar models
Treatment Blind, Study conclusion, Pregnancy information
- StudyEvent: ODM
C2347038 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,2])
C0022423 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
C1519316 (UMLS CUI [1,2])
C1707478 (UMLS CUI [1,2])
C0442603 (UMLS CUI [1,3])
C1524063 (UMLS CUI [1,4])
C1707478 (UMLS CUI [1,2])
C0442603 (UMLS CUI [1,3])
C1524063 (UMLS CUI [1,4])
C1533716 (UMLS CUI-2)
C0086287 (UMLS CUI-3)
C1533716 (UMLS CUI-2)
C0086582 (UMLS CUI-3)
C3887537 (UMLS CUI [1,2])
C3828490 (UMLS CUI [1,3])