ID
40301
Description
Study ID: 110635 Clinical Study ID: 110635 Study Title: A double-blind, randomized, placebo controlled, parallel group, multi-center, phase III trial of ofatumumab investigating clinical efficacy in adult patients with active rheumatoid arthritis who had an inadequate response to methotrexate therapy (FINAL ANALYSIS: follow-up period and cumulative safety data across the whole study) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00611455 Sponsor: GlaxoSmithKline Phase: Phase 3 Study Recruitment Status: Completed Generic Name: ofatumumab, Placebo Study Indication: Arthritis, Rheumatoid
Mots-clés
Versions (1)
- 31/03/2020 31/03/2020 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
31 mars 2020
DOI
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Licence
Creative Commons BY-NC 4.0
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Efficacy of ofatumumab in adult patients with active rheumatoid arthritis with inadequate response to methotrexate NCT00611455
Status of Treatment Blind; Pregnancy Information; Pharmacogenetic Research Withdrawal of Consent; Study Conclusion; Infusion
Description
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Description
If Yes, complete the paper Pregnancy Notification form
Type de données
boolean
Alias
- UMLS CUI [1]
- C3828490
Description
If Yes, complete the paper Pregnancy Notification form Check Not Applicable if female partner not of childbearing potential or no female partner
Type de données
text
Alias
- UMLS CUI [1,1]
- C0919624
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C0008972
Description
Pharmacogenetic Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C1707492
- UMLS CUI-2
- C0031325
Description
If yes, date informed consent withdrawn
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
Description
Date informed consent withdrawn
Type de données
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0011008
Description
Has a request been made for PGx sample destruction?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Description
If a request has been made for PGx sample destruction, check reason
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0392360
Description
Sample type
Type de données
text
Alias
- UMLS CUI [1]
- C2347029
Description
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Description
Date of subject completion or withdrawal
Type de données
date
Alias
- UMLS CUI [1]
- C2983670
Description
If yes, complete primary reason for withdrawal
Type de données
boolean
Alias
- UMLS CUI [1]
- C0422727
Description
Primary reason for withdrawal
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Description
Infusion
Alias
- UMLS CUI-1
- C0574032
Description
If yes was Infusion A or B administered
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0574032
- UMLS CUI [1,2]
- C0545082
Description
Was Infusion A or B administered
Type de données
text
Alias
- UMLS CUI [1]
- C0574032
Similar models
Status of Treatment Blind; Pregnancy Information; Pharmacogenetic Research Withdrawal of Consent; Study Conclusion; Infusion
C2347038 (UMLS CUI-2)
C1264639 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,3])
C0031325 (UMLS CUI-2)
C0031325 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0392360 (UMLS CUI [1,5])
C0392360 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,2])