ID
40301
Descripción
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
Palabras clave
Versiones (1)
- 31/3/20 31/3/20 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
31 de marzo de 2020
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 4.0
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.
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
Descripción
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Descripción
If Yes, complete the paper Pregnancy Notification form
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3828490
Descripción
If Yes, complete the paper Pregnancy Notification form Check Not Applicable if female partner not of childbearing potential or no female partner
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0919624
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C0008972
Descripción
Pharmacogenetic Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C1707492
- UMLS CUI-2
- C0031325
Descripción
If yes, date informed consent withdrawn
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0031325
Descripción
Date informed consent withdrawn
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0011008
Descripción
Has a request been made for PGx sample destruction?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Descripción
If a request has been made for PGx sample destruction, check reason
Tipo de datos
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
Descripción
Sample type
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2347029
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
If yes, complete primary reason for withdrawal
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
Infusion
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])