ID
38810
Beschreibung
Study ID: 111610 Clinical Study ID: 111610 Study Title: A randomised, double-blind, placebo-controlled study in healthy volunteers to examine the safety, tolerability and pharmacokinetics of a) single, ascending and b) twice-daily repeat doses of intranasal SB-705498. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00907933 Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: SB705498, Placebo Study Indication: Rhinitis
Stichworte
Versionen (1)
- 05.11.19 05.11.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
5. November 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Safety, tolerability and pharmacokinetics of single, ascending and twice-daily repeat doses of intranasal SB-705498 NCT00907933
Investigational Product (Period 1 - 5; Day 1 - Day 16)
- StudyEvent: ODM
Beschreibung
Investigational Product (Dose) (Day 1 - 13)
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0178602
Beschreibung
Dose Timepoint
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C2348792
Beschreibung
Start date/time of dose
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [2,1]
- C1301880
- UMLS CUI [2,2]
- C0178602
Beschreibung
Number of Actuations
Datentyp
integer
Alias
- UMLS CUI [1]
- C4055499
Beschreibung
Did the subject receive the correct treatment during this dosing interval?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
Beschreibung
If the subject did not receive the correct treatment during this dosing interval, record reasons.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C0392360
Beschreibung
Investigational Product (Day 3 - Day 13 Dose)
Alias
- UMLS CUI-1
- C0304229
Beschreibung
Dose Timepoint
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2348792
- UMLS CUI [1,2]
- C2348792
Beschreibung
Start date/time of dose
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [2,1]
- C1301880
- UMLS CUI [2,2]
- C0178602
Beschreibung
Number of Actuations
Datentyp
integer
Alias
- UMLS CUI [1]
- C4055499
Beschreibung
Did the subject receive the correct treatment during this dosing interval?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
Beschreibung
If the subject did not receive the correct treatment during this dosing interval, record reasons.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C0392360
Beschreibung
Investigational Product (Dose) (Day 14 - 16)
Alias
- UMLS CUI-1
- C0304229
Beschreibung
Dose Timepoint
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2348792
- UMLS CUI [1,2]
- C2348792
Beschreibung
Start date/time of dose
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [2,1]
- C1301880
- UMLS CUI [2,2]
- C0178602
Beschreibung
Number of Actuations
Datentyp
integer
Alias
- UMLS CUI [1]
- C4055499
Beschreibung
Did the subject receive the correct treatment during this dosing interval?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
Beschreibung
If the subject did not receive the correct treatment during this dosing interval, record reasons.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C0392360
Ähnliche Modelle
Investigational Product (Period 1 - 5; Day 1 - Day 16)
- StudyEvent: ODM
C0040223 (UMLS CUI [1,2])
C0178602 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0087111 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0178602 (UMLS CUI-2)
C0178602 (UMLS CUI [1,2])
C1301880 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0087111 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,2])
C1301880 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0087111 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,2])
C1301880 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0087111 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])