ID
37683
Descripción
Study ID: 105377 Clinical Study ID: 105377 Study Title: A randomised, open-label, parallel-group design study to evaluate the pharmacokinetic characteristics, safety and tolerability of single oral doses of three prototype 300mg enteric coated - modified release formulations of Lamotrigine in healthy subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Lamotrigine Study Indication: Epilepsy
Palabras clave
Versiones (1)
- 16/8/19 16/8/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
16 de agosto de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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Pharmacokinetic characteristics, safety and tolerability of single oral doses of three prototype 300mg enteric coated - modified release formulations of Lamotrigine (Study ID: 105377)
Pharmacogenetics - Research Consent; Research Withdrawal of Consent
Descripción
Pharmacogenetic Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C1707492
- UMLS CUI-2
- C0031325
Descripción
Has subject withdrawn consent for PGx research?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C2347500
Descripción
Has a request been made for sample destruction?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
Descripción
Reason for request for sample destruction
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [1,4]
- C0392360
Descripción
If other reason for request for sample destruction, specify.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1272683
- UMLS CUI [1,4]
- C0392360
- UMLS CUI [1,5]
- C0205394
- UMLS CUI [1,6]
- C2348235
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Pharmacogenetics - Research Consent; Research Withdrawal of Consent
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C1272683 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
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C0392360 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
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C0205394 (UMLS CUI [1,5])
C2348235 (UMLS CUI [1,6])