ID

33872

Description

Study of Nivolumab in Subjects With Relapsed or Refractory Follicular Lymphoma (FL) (CheckMate 140); ODM derived from: https://clinicaltrials.gov/show/NCT02038946

Lien

https://clinicaltrials.gov/show/NCT02038946

Mots-clés

  1. 04/01/2019 04/01/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

4 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Lymphoma NCT02038946

Eligibility Lymphoma NCT02038946

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT02038946
Criteria
Description

Criteria

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
grade 1, 2, or 3a fl without pathologic evidence of transformation
Description

Follicular Lymphoma Grade | Transformation Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0024301
UMLS CUI [1,2]
C0441800
UMLS CUI [2,1]
C1536010
UMLS CUI [2,2]
C0332197
male and female, ages 18 and above, with relapsed or refractory fl lymphoma after > or =2 prior treatment lines; each of the 2 prior treatment lines must include at least cd20 antibody and/or an alkylating agent
Description

Age | Recurrent Follicular Lymphoma | Refractory Follicular Lymphoma | Status post Therapeutic procedure Quantity | Therapeutic procedure Including CD20 Antibody | Therapeutic procedure Including Alkylating Agent

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C1335701
UMLS CUI [3]
C1335723
UMLS CUI [4,1]
C0231290
UMLS CUI [4,2]
C0087111
UMLS CUI [4,3]
C1265611
UMLS CUI [5,1]
C0087111
UMLS CUI [5,2]
C0332257
UMLS CUI [5,3]
C3891557
UMLS CUI [6,1]
C0087111
UMLS CUI [6,2]
C0332257
UMLS CUI [6,3]
C0002073
eastern cooperative oncology group (ecog) performance status (ps) 0-1
Description

ECOG performance status

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known central nervous system lymphoma
Description

Central nervous system lymphoma

Type de données

boolean

Alias
UMLS CUI [1]
C0742472
history of interstitial lung disease
Description

Lung Disease, Interstitial

Type de données

boolean

Alias
UMLS CUI [1]
C0206062
subjects with active, known or suspected autoimmune disease
Description

Autoimmune Disease | Autoimmune Disease Suspected

Type de données

boolean

Alias
UMLS CUI [1]
C0004364
UMLS CUI [2,1]
C0004364
UMLS CUI [2,2]
C0750491
prior allogeneic stem cell transplant
Description

Allogeneic Stem Cell Transplantation

Type de données

boolean

Alias
UMLS CUI [1]
C2242529
prior autologous stem cell transplant ≤12 weeks prior to first dose of study drug
Description

Transplantation of autologous hematopoietic stem cell

Type de données

boolean

Alias
UMLS CUI [1]
C1831743

Similar models

Eligibility Lymphoma NCT02038946

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT02038946
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Item Group
C1512693 (UMLS CUI)
Follicular Lymphoma Grade | Transformation Absent
Item
grade 1, 2, or 3a fl without pathologic evidence of transformation
boolean
C0024301 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C1536010 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Age | Recurrent Follicular Lymphoma | Refractory Follicular Lymphoma | Status post Therapeutic procedure Quantity | Therapeutic procedure Including CD20 Antibody | Therapeutic procedure Including Alkylating Agent
Item
male and female, ages 18 and above, with relapsed or refractory fl lymphoma after > or =2 prior treatment lines; each of the 2 prior treatment lines must include at least cd20 antibody and/or an alkylating agent
boolean
C0001779 (UMLS CUI [1])
C1335701 (UMLS CUI [2])
C1335723 (UMLS CUI [3])
C0231290 (UMLS CUI [4,1])
C0087111 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
C0087111 (UMLS CUI [5,1])
C0332257 (UMLS CUI [5,2])
C3891557 (UMLS CUI [5,3])
C0087111 (UMLS CUI [6,1])
C0332257 (UMLS CUI [6,2])
C0002073 (UMLS CUI [6,3])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance status (ps) 0-1
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Central nervous system lymphoma
Item
known central nervous system lymphoma
boolean
C0742472 (UMLS CUI [1])
Lung Disease, Interstitial
Item
history of interstitial lung disease
boolean
C0206062 (UMLS CUI [1])
Autoimmune Disease | Autoimmune Disease Suspected
Item
subjects with active, known or suspected autoimmune disease
boolean
C0004364 (UMLS CUI [1])
C0004364 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Allogeneic Stem Cell Transplantation
Item
prior allogeneic stem cell transplant
boolean
C2242529 (UMLS CUI [1])
Transplantation of autologous hematopoietic stem cell
Item
prior autologous stem cell transplant ≤12 weeks prior to first dose of study drug
boolean
C1831743 (UMLS CUI [1])

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