ID
33289
Beschrijving
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
Trefwoorden
Versies (3)
- 04-12-18 04-12-18 -
- 07-12-18 07-12-18 -
- 10-12-18 10-12-18 - Sarah Riepenhausen
Houder van rechten
GlaxoSmithKline
Geüploaded op
4 december 2018
DOI
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Licentie
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
Beschrijving
Concomitant medication
Alias
- UMLS CUI-1
- C2347852
Beschrijving
If Yes, record each medication on a separate line using Trade Names where possible in following items. .
Datatype
text
Alias
- UMLS CUI [1,1]
- C1524063
- UMLS CUI [1,2]
- C2347852
Beschrijving
(Trade name preferred)
Datatype
text
Alias
- UMLS CUI [1]
- C0013227
Beschrijving
Unit Dose
Datatype
text
Alias
- UMLS CUI [1]
- C2826646
Beschrijving
Units
Datatype
text
Alias
- UMLS CUI [1]
- C1519795
Beschrijving
Frequency
Datatype
text
Alias
- UMLS CUI [1]
- C3476109
Beschrijving
Route
Datatype
text
Alias
- UMLS CUI [1]
- C0013153
Beschrijving
Reason for medication
Datatype
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0013227
Beschrijving
day month year
Datatype
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Beschrijving
00:00-23:59
Datatype
time
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1301880
Beschrijving
Taken prior to study
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C2347804
Beschrijving
day month year
Datatype
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Beschrijving
00:00-23:59
Datatype
time
Alias
- UMLS CUI [1]
- C2826659
Beschrijving
Ongoing medication
Datatype
text
Alias
- UMLS CUI [1]
- C2826666
Similar models
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])