ID
33477
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 the Concomitant Medications form. It has to be filled in if concomitant medications were taken by subject during study.
Link
https://clinicaltrials.gov/ct2/show/NCT00599612
Stichworte
Versionen (3)
- 04.12.18 04.12.18 -
- 07.12.18 07.12.18 -
- 10.12.18 10.12.18 - Sarah Riepenhausen
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
10. Dezember 2018
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Safety, tolerability, excretion balance and pharmacokinetics of Losmapimod in healthy males, NCT00599612
Concomitant Medications
- StudyEvent: ODM
Beschreibung
Concomitant medication
Alias
- UMLS CUI-1
- C2347852
Beschreibung
If Yes, record each medication on a separate line using Trade Names where possible in following items. .
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1524063
- UMLS CUI [1,2]
- C2347852
Beschreibung
(Trade name preferred)
Datentyp
text
Alias
- UMLS CUI [1]
- C0013227
Beschreibung
Unit Dose
Datentyp
float
Alias
- UMLS CUI [1]
- C0869039
Beschreibung
Units
Datentyp
text
Alias
- UMLS CUI [1]
- C1519795
Beschreibung
Frequency
Datentyp
text
Alias
- UMLS CUI [1]
- C3476109
Beschreibung
Route
Datentyp
text
Alias
- UMLS CUI [1]
- C0013153
Beschreibung
Reason for medication
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0013227
Beschreibung
day month year
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Beschreibung
00:00-23:59
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1301880
Beschreibung
Taken prior to study
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C2347804
Beschreibung
day month year
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Beschreibung
00:00-23:59
Datentyp
time
Alias
- UMLS CUI [1]
- C2826659
Beschreibung
Ongoing medication
Datentyp
text
Alias
- UMLS CUI [1]
- C2826666
Ähnliche Modelle
Concomitant Medications
- StudyEvent: ODM
C2347852 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
C0806020 (UMLS CUI [1,2])