ID

20627

Beschrijving

A Study of Oral LBH589 in Adult Patients With Advanced Hematological Malignancies; ODM derived from: https://clinicaltrials.gov/show/NCT00621244

Link

https://clinicaltrials.gov/show/NCT00621244

Trefwoorden

Versies (1)
  1. 07-03-17 07-03-17 -
Geüploaded op

7 maart 2017

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Lymphoma NCT00621244

Engels

Eligibility Lymphoma NCT00621244

1 Formulieren  
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00621244
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients (≥18 years old) with advanced hematological malignancies who have relapsed after or are refractory to standard therapy, or for which no standard therapy exists; or, are considered inappropriate candidates for standard therapy
Beschrijving

age, advanced hematological malignancies, relapsed after or are refractory to standard therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C0376545
UMLS CUI [2,2]
C0679246
UMLS CUI [3]
C0277556
UMLS CUI [4]
C0205269
world health organization (who) performance status ≤ 2
Beschrijving

who performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1298650
patients must meet protocol-specified hematologic and non-hematologic laboratory values
Beschrijving

laboratory

Datatype

boolean

Alias
UMLS CUI [1]
C0587081
patients must have adequate liver and renal function
Beschrijving

liver function, renal function

Datatype

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0232804
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
concurrent brain metastases or leukemic infiltration of the cerebrospinal fluid
Beschrijving

brain metastases, leukemic infiltration of the cerebrospinal fluid

Datatype

boolean

Alias
UMLS CUI [1]
C0220650
UMLS CUI [2,1]
C0162679
UMLS CUI [2,2]
C0007806
peripheral neuropathy ≥ ctcae grade 2
Beschrijving

peripheral neuropathy

Datatype

boolean

Alias
UMLS CUI [1]
C0031117
unresolved diarrhea ≥ ctcae grade 2
Beschrijving

unresolved diarrhea

Datatype

boolean

Alias
UMLS CUI [1]
C0267664
concurrent severe and/or uncontrolled medical conditions which may compromise participation in the study, including impaired heart function or clinically significant heart disease, and impaired gastrointestinal function or disease that may significantly alter aborption of lbh589
Beschrijving

Comorbidity; Limited (extensiveness); Protocol Compliance | Decreased cardiac function | Heart Diseases | Abnormal digestive tract function; drug absorption

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0525058
UMLS CUI [2]
C0232166
UMLS CUI [3]
C0018799
UMLS CUI [4,1]
C0232459
UMLS CUI [4,2]
C0678745
female patients who are pregnant or breast feeding
Beschrijving

pregnancy, breast feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients not willing to use an effective method of birth control
Beschrijving

contraceptive methods

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
patients taking medications specified by the protocol as prohibited for administration in combination with lbh589
Beschrijving

Pharmaceutical Preparations; Drug Interactions; LBH589

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0687133
UMLS CUI [1,3]
C1566164
patients with another primary malignancy that currently requires active intervention or is currently clinically significant
Beschrijving

Comorbidity; Malignant Neoplasms; Treatment required for

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0006826
UMLS CUI [1,3]
C0332121
other protocol-defined inclusion/exclusion criteria may apply
Beschrijving

ID.13

Datatype

boolean

Terug naar het begin van de pagina

Similar models

Eligibility Lymphoma NCT00621244

1 Formulieren
  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00621244
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age, advanced hematological malignancies, relapsed after or are refractory to standard therapy
Item
adult patients (≥18 years old) with advanced hematological malignancies who have relapsed after or are refractory to standard therapy, or for which no standard therapy exists; or, are considered inappropriate candidates for standard therapy
boolean
C0001779 (UMLS CUI [1])
C0376545 (UMLS CUI [2,1])
C0679246 (UMLS CUI [2,2])
C0277556 (UMLS CUI [3])
C0205269 (UMLS CUI [4])
who performance status
Item
world health organization (who) performance status ≤ 2
boolean
C1298650 (UMLS CUI [1])
laboratory
Item
patients must meet protocol-specified hematologic and non-hematologic laboratory values
boolean
C0587081 (UMLS CUI [1])
liver function, renal function
Item
patients must have adequate liver and renal function
boolean
C0232741 (UMLS CUI [1])
C0232804 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
brain metastases, leukemic infiltration of the cerebrospinal fluid
Item
concurrent brain metastases or leukemic infiltration of the cerebrospinal fluid
boolean
C0220650 (UMLS CUI [1])
C0162679 (UMLS CUI [2,1])
C0007806 (UMLS CUI [2,2])
peripheral neuropathy
Item
peripheral neuropathy ≥ ctcae grade 2
boolean
C0031117 (UMLS CUI [1])
unresolved diarrhea
Item
unresolved diarrhea ≥ ctcae grade 2
boolean
C0267664 (UMLS CUI [1])
Comorbidity; Limited (extensiveness); Protocol Compliance | Decreased cardiac function | Heart Diseases | Abnormal digestive tract function; drug absorption
Item
concurrent severe and/or uncontrolled medical conditions which may compromise participation in the study, including impaired heart function or clinically significant heart disease, and impaired gastrointestinal function or disease that may significantly alter aborption of lbh589
boolean
C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0232166 (UMLS CUI [2])
C0018799 (UMLS CUI [3])
C0232459 (UMLS CUI [4,1])
C0678745 (UMLS CUI [4,2])
pregnancy, breast feeding
Item
female patients who are pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
contraceptive methods
Item
patients not willing to use an effective method of birth control
boolean
C0700589 (UMLS CUI [1])
Pharmaceutical Preparations; Drug Interactions; LBH589
Item
patients taking medications specified by the protocol as prohibited for administration in combination with lbh589
boolean
C0013227 (UMLS CUI [1,1])
C0687133 (UMLS CUI [1,2])
C1566164 (UMLS CUI [1,3])
Comorbidity; Malignant Neoplasms; Treatment required for
Item
patients with another primary malignancy that currently requires active intervention or is currently clinically significant
boolean
C0009488 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
C0332121 (UMLS CUI [1,3])
ID.13
Item
other protocol-defined inclusion/exclusion criteria may apply
boolean
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial