Informações:
Falhas:
ID
25354
Descrição
A Phase I/II Study of BGT226 in Adult Patients With Advanced Solid Malignancies Including Patients With Advanced Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00600275
Link
https://clinicaltrials.gov/show/NCT00600275
Palavras-chave
Versões (1)
- 02/09/2017 02/09/2017 -
Transferido a
2 de setembro de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Solid Tumors NCT00600275
Eligibility Solid Tumors NCT00600275
- StudyEvent: Eligibility
Similar models
Eligibility Solid Tumors NCT00600275
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Patients All
Item
all patients
boolean
C0030705 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
C0444868 (UMLS CUI [1,2])
Solid tumour Advanced
Item
histologically-confirmed, advanced solid tumors
boolean
C0280100 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C0205179 (UMLS CUI [1,2])
Progressive Disease | Recurrent disease unresectable
Item
progressive, recurrent unresectable disease
boolean
C1335499 (UMLS CUI [1])
C0277556 (UMLS CUI [2,1])
C1519810 (UMLS CUI [2,2])
C0277556 (UMLS CUI [2,1])
C1519810 (UMLS CUI [2,2])
Phase 2 Clinical Trial | Advanced breast cancer
Item
phase ii expansion part (advanced breast cancer)
boolean
C0282460 (UMLS CUI [1])
C3495917 (UMLS CUI [2])
C3495917 (UMLS CUI [2])
Hormone Receptor/HER2 Positive | Estrogen receptor positive | Progesterone receptor positive | HER2/Neu Positive
Item
confirmed positive hormone receptor (estrogen receptor and/or progesterone receptor) or positive her-2 expression status
boolean
C3898879 (UMLS CUI [1])
C0279754 (UMLS CUI [2])
C0279759 (UMLS CUI [3])
C2348909 (UMLS CUI [4])
C0279754 (UMLS CUI [2])
C0279759 (UMLS CUI [3])
C2348909 (UMLS CUI [4])
Disease Progression | Recurrent disease | Hormone Therapy Advanced disease | Anti HER2 Advanced disease
Item
disease progression/recurrence following hormonal or anti-her-2 treatment for advanced disease
boolean
C0242656 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
C0279025 (UMLS CUI [3,1])
C0679246 (UMLS CUI [3,2])
C0728747 (UMLS CUI [4,1])
C0679246 (UMLS CUI [4,2])
C0277556 (UMLS CUI [2])
C0279025 (UMLS CUI [3,1])
C0679246 (UMLS CUI [3,2])
C0728747 (UMLS CUI [4,1])
C0679246 (UMLS CUI [4,2])
Chemotherapy Regimen Quantity Unresectable Malignant Neoplasm
Item
at least one but not more than two prior chemotherapy regimens for the unresectable tumor
boolean
C0392920 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1336869 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,2])
C1336869 (UMLS CUI [1,3])
Measurable Disease MRI | Measurable Disease CT scan
Item
measurable disease by mri or ct scan
boolean
C1513041 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C1513041 (UMLS CUI [2,1])
C0040405 (UMLS CUI [2,2])
C0024485 (UMLS CUI [1,2])
C1513041 (UMLS CUI [2,1])
C0040405 (UMLS CUI [2,2])
Cowden Syndrome Advanced
Item
cowden syndrome patients with an advanced malignancy genetic confirmation of cowden syndrome
boolean
C0018553 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C0205179 (UMLS CUI [1,2])
Age
Item
age ≥ 18
boolean
C0001779 (UMLS CUI [1])
WHO performance status scale
Item
world health organization (who) performance status of ≤ 2
boolean
C1298650 (UMLS CUI [1])
Hematopoietic
Item
hematopoietic:
boolean
C0229601 (UMLS CUI [1])
Diabetes Mellitus | History of gestational diabetes mellitus
Item
no diabetes mellitus or history of gestational diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
C2183115 (UMLS CUI [2])
C2183115 (UMLS CUI [2])
Kidney Diseases | Chronic Kidney Diseases
Item
no acute or chronic renal disease
boolean
C0022658 (UMLS CUI [1])
C1561643 (UMLS CUI [2])
C1561643 (UMLS CUI [2])
Liver disease | Chronic liver disease
Item
no acute or chronic liver disease
boolean
C0023895 (UMLS CUI [1])
C0341439 (UMLS CUI [2])
C0341439 (UMLS CUI [2])
Pancreatitis | Pancreatitis, Chronic
Item
no acute or chronic pancreatitis
boolean
C0030305 (UMLS CUI [1])
C0149521 (UMLS CUI [2])
C0149521 (UMLS CUI [2])
Decreased cardiac function | Heart Diseases | Ventricular arrhythmia | Congestive heart failure | Uncontrolled hypertension
Item
no impaired cardiac function or clinically significant cardiac diseases such as ventricular arrhythmia, congestive heart failure, uncontrolled hypertension
boolean
C0232166 (UMLS CUI [1])
C0018799 (UMLS CUI [2])
C0085612 (UMLS CUI [3])
C0018802 (UMLS CUI [4])
C1868885 (UMLS CUI [5])
C0018799 (UMLS CUI [2])
C0085612 (UMLS CUI [3])
C0018802 (UMLS CUI [4])
C1868885 (UMLS CUI [5])
Myocardial Infarction | Angina, Unstable
Item
no acute myocardial infarction or unstable angina pectoris within the past 3 months
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0002965 (UMLS CUI [2])
Pregnancy | Breast Feeding | Fertility Barrier Contraception
Item
not pregnant or nursing and fertile patients must use barrier contraceptives
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0015895 (UMLS CUI [3,1])
C0004764 (UMLS CUI [3,2])
C0006147 (UMLS CUI [2])
C0015895 (UMLS CUI [3,1])
C0004764 (UMLS CUI [3,2])
Clinical Trial Eligibility Criteria Study Protocol
Item
other protocol-defined inclusion/exclusion criteria may apply.
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,2])