ID
41096
Descripción
Study ID: 103447 Clinical Study ID: NKV103447 Study Title:A study to evaluate the effect of casoptiant on cardiac conduction as assessed by 12-lead electrocardiogram as compared to placebo and moxifloxacin Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: casopitant Trade Name: Rezonic,Zunrisa; Zunrisa,Rezonic Study Indication: Nausea and Vomiting, Chemotherapy-Induced
Palabras clave
Versiones (1)
- 23/6/20 23/6/20 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
23 de junio de 2020
DOI
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Licencia
Creative Commons BY-NC 4.0
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Effect of casoptiant on cardiac conduction as compared to placebo and moxifloxacin 103447
Study Conclusion; Pregnancy Information; Investigator Comment Log, Investigator's Signature
Descripción
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Descripción
Date of subject completion or withdrawal
Tipo de datos
date
Alias
- UMLS CUI [1]
- C2983670
Descripción
Time of withdrawal
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0040223
Descripción
Was the subject withdrawn from the study?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0422727
Descripción
Primary reason for withdrawal
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Descripción
If other reason for withdrawal, specify
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Descripción
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Descripción
If Yes, complete Pregnancy Notification form.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3828490
Descripción
If Yes, complete Pregnancy Notification form.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0919624
Descripción
Investigator Comment Log
Alias
- UMLS CUI-1
- C0008961
- UMLS CUI-2
- C0947611
Descripción
Investigator's Signature
Alias
- UMLS CUI-1
- C2346576
Descripción
I confirm that I have reviewed the data in this Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, complete and accurate, as of the date below.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2346576
Descripción
Investigator’s name
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826892
Descripción
Investigator's Signature Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
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Study Conclusion; Pregnancy Information; Investigator Comment Log, Investigator's Signature
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C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0947611 (UMLS CUI-2)
C1516308 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])