ID
33385
Beschreibung
Study ID: 107806 Clinical Study ID: RA3107806 Study Title: An open label study to determine the safety, tolerability, excretion balance and pharmacokinetics of Losmapimod, administered as a single dose of an oral solution to healthy adult male subjects Patient Level Data: Clinicaltrials.gov Identifier: NCT00599612 https://clinicaltrials.gov/ct2/show/NCT00599612 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: losmapimod Trade Name: losmapimod Study Indication: Pulmonary Disease, Chronic Obstructive The study consists of a screening, study visit and follow-up. The protocol identifier for all: RA3107806 This document contains Study conclusion, Investigator Comment Log, Investigator's signature. It has to be filled in for the end of study.
Link
https://clinicaltrials.gov/ct2/show/NCT00599612
Stichworte
Versionen (2)
- 07.12.18 07.12.18 -
- 11.12.18 11.12.18 - Sarah Riepenhausen
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
7. Dezember 2018
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY-NC 3.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Safety, tolerability, excretion balance and pharmacokinetics of Losmapimod in healthy males, NCT00599612
Study conclusion, Investigator Comment Log, Investigator's signature
Beschreibung
Study conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Beschreibung
day month year
Datentyp
date
Alias
- UMLS CUI [1]
- C1549507
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C0422727
Beschreibung
Subject's withdraw
Datentyp
text
Alias
- UMLS CUI [1]
- C2349954
Beschreibung
If you tick 1: Record details on the Non-Serious Adverse Events or Serious Adverse Event pages as appropriate. To 6 and 7: Only tick if none of the other primary reasons are appropriate
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0566251
Beschreibung
Investigator discretion, specification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0008961
- UMLS CUI [1,2]
- C0022423
- UMLS CUI [2,1]
- C2349954
- UMLS CUI [2,2]
- C0566251
Beschreibung
Withdrew consent , specification
Datentyp
text
Alias
- UMLS CUI [1]
- C1707492
- UMLS CUI [2,1]
- C2349954
- UMLS CUI [2,2]
- C0566251
Beschreibung
Investigator Comment Log
Alias
- UMLS CUI-1
- C0008961
- UMLS CUI-2
- C0947611
Beschreibung
Investigator's signature
Alias
- UMLS CUI-1
- C2346576
Beschreibung
Confirmation complete data in CRF
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C3899518
Beschreibung
Investigator's signature
Datentyp
text
Alias
- UMLS CUI [1]
- C2346576
Beschreibung
Investigator's name (print)
Datentyp
text
Alias
- UMLS CUI [1]
- C2826892
Beschreibung
day month year
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Ähnliche Modelle
Study conclusion, Investigator Comment Log, Investigator's signature
C0011008 (UMLS CUI [2,1])
C0422727 (UMLS CUI [2,2])
C0566251 (UMLS CUI [1,2])
C0022423 (UMLS CUI [1,2])
C2349954 (UMLS CUI [2,1])
C0566251 (UMLS CUI [2,2])
C2349954 (UMLS CUI [2,1])
C0566251 (UMLS CUI [2,2])
C0947611 (UMLS CUI-2)
C1516308 (UMLS CUI [1,2])
C3899518 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])