ID
41044
Descripción
This form documents the concomitant medications taken during the study. To be filled in continously. 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
Palabras clave
Versiones (1)
- 16/6/20 16/6/20 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
16 de junio de 2020
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 4.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
Sumatriptan pharmacokinetics for TREXIMA/IMITREX ID 103629
Concomitant Medications
- StudyEvent: ODM
Descripción
Concomintant Medications
Alias
- UMLS CUI-1
- C2347852
Descripción
Concomitant Agent Drug Name
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Descripción
Concomitant Agent Unit Dose
Tipo de datos
float
Alias
- UMLS CUI [1]
- C2826646
Descripción
Concomitant Agent Unit
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0439148
Descripción
Concomitant Agent Frequency
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826654
Descripción
Concomitant Agent Drug Administration Routes
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0013153
Descripción
Concomitant Agent Indication
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C3146298
Descripción
Hr:Min (00:00-23:59)
Tipo de datos
datetime
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Descripción
Concomitant Agent Taken Prior to Study?
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826667
Descripción
Concomitant Agent Ongoing
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826666
Descripción
Hr:Min (00:00-23:59) To be filled in if the angent is not ongoing.
Tipo de datos
datetime
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0806020
- UMLS CUI [1,3]
- C1522314
Similar models
Concomitant Medications
- StudyEvent: ODM
C2360065 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
C0806020 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,3])
Sin comentarios