ID
15682
Beschrijving
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)
Trefwoorden
Versies (1)
- 08-06-16 08-06-16 -
Geüploaded op
8 juni 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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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
Beschrijving
Inclusion/Exclusion
Beschrijving
Protocol Version
Datatype
text
Alias
- UMLS CUI [1]
- C2985700
Beschrijving
informed consent date
Datatype
text
Alias
- UMLS CUI [1]
- C2985782
Beschrijving
If no, record the unmet criterion numbers as indicated in the protocol.
Datatype
boolean
Alias
- UMLS CUI [1]
- C1516637
Beschrijving
Inclusion Criteria
Datatype
text
Alias
- UMLS CUI [1]
- C1512693
Beschrijving
Inclusion Criteria
Datatype
text
Alias
- UMLS CUI [1]
- C1512693
Beschrijving
Inclusion Criteria
Datatype
text
Alias
- UMLS CUI [1]
- C1512693
Beschrijving
Exclusion Criteria
Datatype
text
Alias
- UMLS CUI [1]
- C0680251
Beschrijving
Exclusion Criteria
Datatype
text
Alias
- UMLS CUI [1]
- C0680251
Beschrijving
Exclusion Criteria
Datatype
text
Alias
- UMLS CUI [1]
- C0680251
Beschrijving
Exclusion Criteria
Datatype
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])