ID
15682
Descripción
The primary objective of this study is to evaluate the long-term safety profile of BG00012 (dimethyl fumarate). Secondary objectives of this study are to evaluate the long-term efficacy of BG00012 using clinical endpoints and disability progression, to evaluate further the long-term effects of BG00012 on multiple sclerosis (MS) brain lesions on magnetic resonance imaging (MRI) scans in participants who had MRI scans as part of Studies 109MS301 (NCT00420212) and 109MS302 (NCT00451451) and to evaluate the long-term effects of BG00012 on health economics assessments and the visual function test. NCT00835770 Part: Baseline Visit (Day 1)
Palabras clave
Versiones (1)
- 8/6/16 8/6/16 -
Subido en
8 de junio de 2016
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 3.0
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.
Baseline Visit (Day 1): Inclusion/Exclusion BG00012 Monotherapy Safety and Efficacy Extension Study in Multiple Sclerosis (MS) (ENDORSE) NCT00835770
Baseline Visit (Day 1): Inclusion/Exclusion BG00012 Monotherapy Safety and Efficacy Extension Study in Multiple Sclerosis (MS) (ENDORSE) NCT00835770
Descripción
Inclusion/Exclusion
Descripción
Protocol Version
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2985700
Descripción
informed consent date
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2985782
Descripción
If no, record the unmet criterion numbers as indicated in the protocol.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1516637
Descripción
Inclusion Criteria
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1512693
Descripción
Inclusion Criteria
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1512693
Descripción
Inclusion Criteria
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1512693
Descripción
Exclusion Criteria
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0680251
Descripción
Exclusion Criteria
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0680251
Descripción
Exclusion Criteria
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0680251
Descripción
Exclusion Criteria
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0680251
Similar models
Baseline Visit (Day 1): Inclusion/Exclusion BG00012 Monotherapy Safety and Efficacy Extension Study in Multiple Sclerosis (MS) (ENDORSE) NCT00835770
C0600091 (UMLS CUI [1,2])