ID

14628

Beschrijving

Global Phase1 Study to Assess the Safety and Tolerability of AZD1208 in Advanced Solid Tumors and Malignant Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT01588548

Link

https://clinicaltrials.gov/show/NCT01588548

Trefwoorden

  1. 24-04-16 24-04-16 -
Geüploaded op

24 april 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Advanced Solid Malignancies NCT01588548

Eligibility Advanced Solid Malignancies NCT01588548

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who have signed this written informed consent form after a full explanation about the participation in this study
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
patients aged 18 years or older patients diagnosed with a solid malignant tumour or malignant lymphoma that is refractory to standard therapies or for which no standard therapies exist
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
patients with good physical conditions (you can walk and can look after yourself) within the last 2 weeks.
Beschrijving

physical condition

Datatype

boolean

Alias
UMLS CUI [1]
C1142435
patients who have at least one lesion that can be accurately assessed
Beschrijving

lesion

Datatype

boolean

Alias
UMLS CUI [1]
C0221198
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who have recently received or are receiving prohibited medications or treatments
Beschrijving

prohibited medications or treatments

Datatype

boolean

Alias
UMLS CUI [1,1]
C0138547
UMLS CUI [1,2]
C0013227
patients who have any unresolved side effects of previous treatments
Beschrijving

unresolved side effects

Datatype

boolean

Alias
UMLS CUI [1]
C0879626
patients who have spinal cord compression or brain metastases
Beschrijving

spinal cord compression or brain metastases

Datatype

boolean

Alias
UMLS CUI [1]
C0037926
UMLS CUI [2]
C0220650
patients who have severe systemic diseases (e.g., uncontrolled hypertension, hepatitis b, hepatitis c and human immunodeficiency virus [hiv] infection)
Beschrijving

severe systemic diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0442893
patients with significant abnormal ecg findings
Beschrijving

ecg findings

Datatype

boolean

Alias
UMLS CUI [1]
C0438154

Similar models

Eligibility Advanced Solid Malignancies NCT01588548

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
informed consent
Item
patients who have signed this written informed consent form after a full explanation about the participation in this study
boolean
C0021430 (UMLS CUI [1])
age
Item
patients aged 18 years or older patients diagnosed with a solid malignant tumour or malignant lymphoma that is refractory to standard therapies or for which no standard therapies exist
boolean
C0001779 (UMLS CUI [1])
physical condition
Item
patients with good physical conditions (you can walk and can look after yourself) within the last 2 weeks.
boolean
C1142435 (UMLS CUI [1])
lesion
Item
patients who have at least one lesion that can be accurately assessed
boolean
C0221198 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
prohibited medications or treatments
Item
patients who have recently received or are receiving prohibited medications or treatments
boolean
C0138547 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
unresolved side effects
Item
patients who have any unresolved side effects of previous treatments
boolean
C0879626 (UMLS CUI [1])
spinal cord compression or brain metastases
Item
patients who have spinal cord compression or brain metastases
boolean
C0037926 (UMLS CUI [1])
C0220650 (UMLS CUI [2])
severe systemic diseases
Item
patients who have severe systemic diseases (e.g., uncontrolled hypertension, hepatitis b, hepatitis c and human immunodeficiency virus [hiv] infection)
boolean
C0442893 (UMLS CUI [1])
ecg findings
Item
patients with significant abnormal ecg findings
boolean
C0438154 (UMLS CUI [1])

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