ID
37520
Beschrijving
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
Trefwoorden
Versies (1)
- 04-08-19 04-08-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
4 augustus 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Evaluation of Naproxen Sodium and Sumatriptan in Adolescent Subjects With Migraine and Healthy Adult Subjects NCT00989625
Dose - Randomisation Number; Investigational Product
- StudyEvent: ODM
Beschrijving
Investigational Product
Alias
- UMLS CUI-1
- C0304229
Beschrijving
Date/time of dose
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C1264639
Beschrijving
Investigational Product
Datatype
integer
Alias
- UMLS CUI [1]
- C0304229
Beschrijving
Did the subject receive the correct treatment
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [2,1]
- C0178602
- UMLS CUI [2,2]
- C1272706
Beschrijving
If subject did not receive the correct treatment, record reason(s)
Datatype
text
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [2]
- C0392360
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Dose - Randomisation Number; Investigational Product
- StudyEvent: ODM
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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])