ID

13245

Beschrijving

Phase 1b Acute Myelogenous Leukemia (AML) Study With ABT-199 + Decitabine or Azacitidine (Chemo Combo); ODM derived from: https://clinicaltrials.gov/show/NCT02203773

Link

https://clinicaltrials.gov/show/NCT02203773

Trefwoorden

Versies (1)
  1. 26-01-16 26-01-16 -
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CC BY-NC 3.0

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26 januari 2016

DOI

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Creative Commons BY-NC 3.0
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Eligibility Acute Myelogenous Leukemia NCT02203773

Engels

Eligibility Acute Myelogenous Leukemia NCT02203773

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. subjects must have histological confirmation of aml by who criteria and be ineligible for treatment with a standard cytarabine and anthracycline induction regimen due to co-morbidity or other factors.
Beschrijving

AML

Datatype

boolean

Alias
UMLS CUI [1]
C0023467
2. subjects must have received no prior treatment for aml with the exception of hydroxyurea, allowed through the first cycle of study treatment. note: subject may have been treated for prior myelodysplastic syndrome (excluding hypomethylating agents).
Beschrijving

prior treatment

Datatype

boolean

Alias
UMLS CUI [1]
C0087111
3. subjects must have an eastern cooperative oncology group (ecog) performance status of 0 to 2.
Beschrijving

ECOG

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
4. subject must have adequate renal function as demonstrated by a calculated creatinine clearance ≥ 50 ml/min; determined via urine collection for 24-hour creatinine clearance or by the cockcroft gault formula.
Beschrijving

renal function

Datatype

boolean

Alias
UMLS CUI [1]
C0373595
5. subject must have adequate liver function.
Beschrijving

liver function

Datatype

boolean

Alias
UMLS CUI [1]
C0232741
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. subject has received treatment with a hypomethylating agent and/or cytarabine for a pre-existing myeloid disorder.
Beschrijving

hypomethylating agent and/or cytarabine

Datatype

boolean

Alias
UMLS CUI [1]
C0010711
2. subject must not have favorable risk cytogenetics as categorized by the nccn guidelines version 2, 2014 for acute myeloid leukemia.
Beschrijving

risk cytogenetics

Datatype

boolean

Alias
UMLS CUI [1]
C0010802
3. subject has t(8;21), inv(16) or t(15;17) karyotype abnormalities.
Beschrijving

karyotype abnormalities

Datatype

boolean

Alias
UMLS CUI [1]
C1261273
4. subject has acute promyelocytic leukemia (french-american-british class m3 aml).
Beschrijving

APL

Datatype

boolean

Alias
UMLS CUI [1]
C0023487
5. subject has known active cns involvement with aml.
Beschrijving

CNS Leukemia

Datatype

boolean

Alias
UMLS CUI [1]
C1332884
6. subject has received the following within 7 days prior to the initiation of study treatment: potent cyp3a inducers such as rifampin, carbamazepine, phenytoin, and st. john's wort; warfarin or requires the use of warfarin and its equivalent drugs, such as phenprocoumon; (due to potential drug-drug interactions that may potentially increase the exposure of warfarin and complications of anticoagulant effect). cyp3a inhibitors such as fluconazole, ketoconazole, and clarithromycin.
Beschrijving

CYP3A interactions, warfarin

Datatype

boolean

Alias
UMLS CUI [1]
C3830624
UMLS CUI [2]
C3830625
UMLS CUI [3]
C0043031
7. subject has a history of other malignancies prior to study entry, with the exception of: adequately treated in situ carcinoma of the cervix uteri or carcinoma in situ of breast; basal cell carcinoma of the skin or localized squamous cell carcinoma of the skin; previous malignancy confined and surgically resected (or treated with other modalities) with curative intent.
Beschrijving

prior malignancy

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
8. subject has a white blood cell count > 25 × 10^9/l. note: hydroxyurea is permitted to meet this criterion.
Beschrijving

leukocytes

Datatype

boolean

Alias
UMLS CUI [1]
C0023508
9. subject is a candidate for a bone marrow or stem cell transplant within 12 weeks after study enrollment.
Beschrijving

one marrow or stem cell transplant

Datatype

boolean

Alias
UMLS CUI [1]
C0005961
UMLS CUI [2]
C1504389
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Similar models

Eligibility Acute Myelogenous Leukemia NCT02203773

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
AML
Item
1. subjects must have histological confirmation of aml by who criteria and be ineligible for treatment with a standard cytarabine and anthracycline induction regimen due to co-morbidity or other factors.
boolean
C0023467 (UMLS CUI [1])
prior treatment
Item
2. subjects must have received no prior treatment for aml with the exception of hydroxyurea, allowed through the first cycle of study treatment. note: subject may have been treated for prior myelodysplastic syndrome (excluding hypomethylating agents).
boolean
C0087111 (UMLS CUI [1])
ECOG
Item
3. subjects must have an eastern cooperative oncology group (ecog) performance status of 0 to 2.
boolean
C1520224 (UMLS CUI [1])
renal function
Item
4. subject must have adequate renal function as demonstrated by a calculated creatinine clearance ≥ 50 ml/min; determined via urine collection for 24-hour creatinine clearance or by the cockcroft gault formula.
boolean
C0373595 (UMLS CUI [1])
liver function
Item
5. subject must have adequate liver function.
boolean
C0232741 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
hypomethylating agent and/or cytarabine
Item
1. subject has received treatment with a hypomethylating agent and/or cytarabine for a pre-existing myeloid disorder.
boolean
C0010711 (UMLS CUI [1])
risk cytogenetics
Item
2. subject must not have favorable risk cytogenetics as categorized by the nccn guidelines version 2, 2014 for acute myeloid leukemia.
boolean
C0010802 (UMLS CUI [1])
karyotype abnormalities
Item
3. subject has t(8;21), inv(16) or t(15;17) karyotype abnormalities.
boolean
C1261273 (UMLS CUI [1])
APL
Item
4. subject has acute promyelocytic leukemia (french-american-british class m3 aml).
boolean
C0023487 (UMLS CUI [1])
CNS Leukemia
Item
5. subject has known active cns involvement with aml.
boolean
C1332884 (UMLS CUI [1])
CYP3A interactions, warfarin
Item
6. subject has received the following within 7 days prior to the initiation of study treatment: potent cyp3a inducers such as rifampin, carbamazepine, phenytoin, and st. john's wort; warfarin or requires the use of warfarin and its equivalent drugs, such as phenprocoumon; (due to potential drug-drug interactions that may potentially increase the exposure of warfarin and complications of anticoagulant effect). cyp3a inhibitors such as fluconazole, ketoconazole, and clarithromycin.
boolean
C3830624 (UMLS CUI [1])
C3830625 (UMLS CUI [2])
C0043031 (UMLS CUI [3])
prior malignancy
Item
7. subject has a history of other malignancies prior to study entry, with the exception of: adequately treated in situ carcinoma of the cervix uteri or carcinoma in situ of breast; basal cell carcinoma of the skin or localized squamous cell carcinoma of the skin; previous malignancy confined and surgically resected (or treated with other modalities) with curative intent.
boolean
C0006826 (UMLS CUI [1])
leukocytes
Item
8. subject has a white blood cell count > 25 × 10^9/l. note: hydroxyurea is permitted to meet this criterion.
boolean
C0023508 (UMLS CUI [1])
one marrow or stem cell transplant
Item
9. subject is a candidate for a bone marrow or stem cell transplant within 12 weeks after study enrollment.
boolean
C0005961 (UMLS CUI [1])
C1504389 (UMLS CUI [2])
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