ID
33053
Descrizione
This form contains a form to document the study conclusion and pregnancy information. To be assessed at the follow-up visit. 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
collegamento
https://clinicaltrials.gov/ct2/show/NCT00875784
Keywords
versioni (2)
- 25/11/18 25/11/18 -
- 25/11/18 25/11/18 -
Titolare del copyright
GlaxoSmithKline
Caricato su
25 novembre 2018
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 3.0
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Sumatriptan pharmacokinetics for TREXIMA/IMITREX NCT00875784
Study Conclusion and Pregnancy Information
- StudyEvent: ODM
Descrizione
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008976
Descrizione
Date of subject completion or withdrawal
Tipo di dati
date
Alias
- UMLS CUI [1]
- C2983670
Descrizione
If yes, complete primary reason for witltdrawal
Tipo di dati
text
Alias
- UMLS CUI [1]
- C0422727
Descrizione
In case you tick Adverse Event: Record details on the Non-Serious Adverse Events or Serious Adverse Events forms as appropriate. In case you tick Investigator discretion, specify in the next item. Select this reason if none of the other primary reasons are appropriate.
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Descrizione
Withdrawal from the study at the investigator's discretion, specification
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C1710220
- UMLS CUI [1,3]
- C0679006
- UMLS CUI [1,4]
- C2348235
Descrizione
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Descrizione
if Yes, complete the paper Pregnancy Notification form Check Not Applicable iffemale partner not of childbearing potential or no female partner
Tipo di dati
text
Alias
- UMLS CUI [1]
- C0919624
Descrizione
If Yes, complete the paper Pregnancy Notification form
Tipo di dati
text
Alias
- UMLS CUI [1]
- C0032961
Similar models
Study Conclusion and Pregnancy Information
- StudyEvent: ODM
C0392360 (UMLS CUI [1,2])
C1710220 (UMLS CUI [1,2])
C0679006 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])