ID
37520
Beschreibung
Study ID: 108504 Clinical Study ID: 108504 Study Title: An Open Label, Single Dose, Randomised, Parallel Group Pharmacokinetic Study to Evaluate a Combination Product Containing Naproxen Sodium and Sumatriptan in Adolescent Subjects With Migraine and Healthy Adult Subjects Administered at Three Doses. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00989625 Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: This is a pharmacokinetic study (Treximet) Trade Name: Naproxen Sodium and Sumatriptan Study Indication: Migraine Disorders
Stichworte
Versionen (1)
- 04.08.19 04.08.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
4. August 2019
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.
Evaluation of Naproxen Sodium and Sumatriptan in Adolescent Subjects With Migraine and Healthy Adult Subjects NCT00989625
Dose - Randomisation Number; Investigational Product
- StudyEvent: ODM
Beschreibung
Investigational Product
Alias
- UMLS CUI-1
- C0304229
Beschreibung
Date/time of dose
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C1264639
Beschreibung
Investigational Product
Datentyp
integer
Alias
- UMLS CUI [1]
- C0304229
Beschreibung
Did the subject receive the correct treatment
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [2,1]
- C0178602
- UMLS CUI [2,2]
- C1272706
Beschreibung
If subject did not receive the correct treatment, record reason(s)
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [2]
- C0392360
Ähnliche Modelle
Dose - Randomisation Number; Investigational Product
- StudyEvent: ODM
C0085732 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0087111 (UMLS CUI [1,2])
C0178602 (UMLS CUI [2,1])
C1272706 (UMLS CUI [2,2])
C0087111 (UMLS CUI [1,2])
C0392360 (UMLS CUI [2])