ID
41049
Description
This form documents if pharmacokinetics measurement was repeated. To be filled in after doing the repeated measurement (or at study conclusion). Study ID: 103629 Clinical Study ID: TRX103629 Study Title: An open-label, randomized, 3-period crossover study to evaluate sumatriptan and naproxen pharmacokinetics for a combination tablet product containing sumatriptan/naproxen sodium followed by IMITREX™ (sumatriptan succinate) Injection 4mg administered using the IMITREX STATdose System and a sumatriptan/naproxen sodium tablet followed by IMITREX (sumatriptan succinate) Injection 6mg administered using the STATdose system compared with an IMITREX tablet 100mg followed by an IMITREX tablet 100mg Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00875784 Clinicaltrials.gov link: https://clinicaltrials.gov/ct2/show/NCT00875784 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: sumatriptan Trade Name: Imitrex ,Imiject ,Imigran; Imitrex,Imiject,Imigran Study Indication: Migraine Disorders
Link
https://clinicaltrials.gov/ct2/show/NCT00875784
Keywords
Versions (1)
- 6/16/20 6/16/20 -
Copyright Holder
GlaxoSmithKline
Uploaded on
June 16, 2020
DOI
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License
Creative Commons BY-NC 4.0
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Sumatriptan pharmacokinetics for TREXIMA/IMITREX ID 103629
Repeat Pharmacokinetics Blood
- StudyEvent: ODM
Description
REPEAT PHARMACOKINETICS BLOOD
Alias
- UMLS CUI-1
- C0031328
- UMLS CUI-2
- C0005767
- UMLS CUI-3
- C0205341
Similar models
Repeat Pharmacokinetics Blood
- StudyEvent: ODM
C0005767 (UMLS CUI-2)
C0205341 (UMLS CUI-3)
C0005767 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
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