ID

32391

Descripción

Safety and Efficacy of GMX1777 in the Treatment of Refractory Solid Tumors or Lymphomas; ODM derived from: https://clinicaltrials.gov/show/NCT00457574

Link

https://clinicaltrials.gov/show/NCT00457574

Palabras clave

  1. 29/10/18 29/10/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

29 de octubre de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 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.

Eligibility Solid Tumors and Lymphomas NCT00457574

Eligibility Solid Tumors and Lymphomas NCT00457574

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must have a histologically or cytologically confirmed solid tumor or lymphoma
Descripción

Solid Neoplasm | Lymphoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0280100
UMLS CUI [2]
C0024299
no limitations on allowable type and amount of prior therapy.
Descripción

Limitation Absent Prior Therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0449295
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C1514463
patients must have a life expectancy of greater than 8 weeks
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
patients must have normal organ and marrow function
Descripción

Organ function | Bone Marrow function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678852
UMLS CUI [2,1]
C0005953
UMLS CUI [2,2]
C0031843
patients must be willing to submit blood sampling for planned pk analysis
Descripción

Blood sampling Pharmacokinetic aspects

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0031328
patients must have the ability to understand and willingness to sign a written informed consent form
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
no other agents or therapies administered with the intent to treat malignancy
Descripción

Pharmaceutical Preparations Other Cancer treatment | Cancer treatment Other

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C0920425
UMLS CUI [2,1]
C0920425
UMLS CUI [2,2]
C0205394
patients with prior exposure to gmx1777 or gmx1778
Descripción

Exposure to GMX1777 | Exposure to GMX 1778

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332157
UMLS CUI [1,2]
C2346839
UMLS CUI [2,1]
C0332157
UMLS CUI [2,2]
C2713488
uncontrolled, intercurrent illness
Descripción

Comorbidity Uncontrolled

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205318
pregnant women and women who are breast feeding
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147

Similar models

Eligibility Solid Tumors and Lymphomas NCT00457574

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Solid Neoplasm | Lymphoma
Item
patients must have a histologically or cytologically confirmed solid tumor or lymphoma
boolean
C0280100 (UMLS CUI [1])
C0024299 (UMLS CUI [2])
Limitation Absent Prior Therapy
Item
no limitations on allowable type and amount of prior therapy.
boolean
C0449295 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1514463 (UMLS CUI [1,3])
Life Expectancy
Item
patients must have a life expectancy of greater than 8 weeks
boolean
C0023671 (UMLS CUI [1])
Organ function | Bone Marrow function
Item
patients must have normal organ and marrow function
boolean
C0678852 (UMLS CUI [1])
C0005953 (UMLS CUI [2,1])
C0031843 (UMLS CUI [2,2])
Blood sampling Pharmacokinetic aspects
Item
patients must be willing to submit blood sampling for planned pk analysis
boolean
C0005834 (UMLS CUI [1,1])
C0031328 (UMLS CUI [1,2])
Informed Consent
Item
patients must have the ability to understand and willingness to sign a written informed consent form
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pharmaceutical Preparations Other Cancer treatment | Cancer treatment Other
Item
no other agents or therapies administered with the intent to treat malignancy
boolean
C0013227 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,3])
C0920425 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
Exposure to GMX1777 | Exposure to GMX 1778
Item
patients with prior exposure to gmx1777 or gmx1778
boolean
C0332157 (UMLS CUI [1,1])
C2346839 (UMLS CUI [1,2])
C0332157 (UMLS CUI [2,1])
C2713488 (UMLS CUI [2,2])
Comorbidity Uncontrolled
Item
uncontrolled, intercurrent illness
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant women and women who are breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

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