ID

15383

Description

Cord Blood Natural Killer (NK) Cells in Chronic Lymphocytic Leukemia (CLL); ODM derived from: https://clinicaltrials.gov/show/NCT02280525

Lien

https://clinicaltrials.gov/show/NCT02280525

Mots-clés

Versions (1)
  1. 29/05/2016 29/05/2016 -
Téléchargé le

29 mai 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Leukemia NCT02280525

Anglais

Eligibility Leukemia NCT02280525

1 Formulaires  
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT02280525
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. patients with history of b-cll who have received at least 2 lines of standard chemoimmunotherapy and have persistent disease.
Description

Chronic Lymphocytic Leukemia | Chemoimmunotherapy Standard | Persistent Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0023434
UMLS CUI [2,1]
C2986423
UMLS CUI [2,2]
C1442989
UMLS CUI [3]
C2983415
2. patients with acute lymphoblastic leukemia (all), acute myelogenous leukemia (aml), chronic myelogenous leukemia (cml) with relapsed or refractory disease.
Description

Acute lymphocytic leukemia | Leukemia, Myelocytic, Acute | Myeloid Leukemia, Chronic | Recurrent disease | Refractory Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0023449
UMLS CUI [2]
C0023467
UMLS CUI [3]
C0023473
UMLS CUI [4]
C0277556
UMLS CUI [5]
C1514815
3. patients with histologically confirmed aggressive b cell nhl with chemotherapy-refractory disease. chemotherapy refractory disease is defined as one or more of the following: stable disease or progressive disease as best response to most recent chemotherapy containing regimen or disease progression or recurrence within 12 months of prior autologous or allogeneic stem cell transplant. subjects must have received adequate prior therapy including at a minimum: anti-cd20 monoclonal antibody unless tumor is cd20-negative, an anthracycline containing chemotherapy regimen. subjects with transformed fl must have received prior chemotherapy for follicular lymphoma and subsequently have chemo-refractory disease after transformation to diffuse large b-cell lymphoma (dlbcl).
Description

B-Cell Lymphomas | Chemotherapy Regimen | Refractory Disease | autologous hematopoietic stem cell transplant | allogenic hematopoietic stem cell transplant | rituximab | Chemotherapy Regimen Anthracyclines | Lymphoma, Follicular | Diffuse Large B-Cell Lymphoma

Type de données

boolean

Alias
UMLS CUI [1]
C0079731
UMLS CUI [2]
C0392920
UMLS CUI [3]
C1514815
UMLS CUI [4]
C2193200
UMLS CUI [5]
C1456094
UMLS CUI [6]
C0393022
UMLS CUI [7,1]
C0392920
UMLS CUI [7,2]
C0282564
UMLS CUI [8]
C0024301
UMLS CUI [9]
C0079744
4. patient with hodgkin's lymphoma with relapsed or refractory disease.
Description

Hodgkin Disease | Recurrent disease | Refractory Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0019829
UMLS CUI [2]
C0277556
UMLS CUI [3]
C1514815
5. patients who are at least 3 weeks from the time of consent. patients may continue ibrutinib, idelalisib, or lenalidomide till the day of study consent.
Description

Ibrutinib | idelalisib | lenalidomide

Type de données

boolean

Alias
UMLS CUI [1]
C3501358
UMLS CUI [2]
C2698692
UMLS CUI [3]
C1144149
6. karnofsky performance scale > 60%.
Description

Karnofsky Performance Status

Type de données

boolean

Alias
UMLS CUI [1]
C0206065
7. adequate hepatic function, as defined by sgpt <3 x upper limit of normal; serum bilirubin and alkaline phosphatase <2 x upper limit of normal, or considered not clinically significant by the study doctor or designee, serum creatinine of </=2 mg/dl.
Description

Liver function | Alanine aminotransferase measurement | Serum total bilirubin measurement | Alkaline phosphatase measurement | Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0201836
UMLS CUI [3]
C1278039
UMLS CUI [4]
C0201850
UMLS CUI [5]
C0201976
8. able to provide written informed consent.
Description

Informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
9. 18-80 years of age.
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
10. all study participants must be registered into the mandatory revlimid remstm program, and be willing and able to comply with the requirements of the revlimid remstm program. females of childbearing potential must adhere to the scheduled pregnancy testing and contraception as required in the revlimid remstm program. a female of childbearing potential (fcbp) is a sexually mature female who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).
Description

Revlimid Program | Compliance behavior | Childbearing Potential Pregnancy Test Contraceptive methods | Hysterectomy | Bilateral oophorectomy | Postmenopausal state | Menstruation

Type de données

boolean

Alias
UMLS CUI [1,1]
C1135145
UMLS CUI [1,2]
C3484370
UMLS CUI [2]
C1321605
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0032976
UMLS CUI [3,3]
C0700589
UMLS CUI [4]
C0020699
UMLS CUI [5]
C0278321
UMLS CUI [6]
C0232970
UMLS CUI [7]
C0025344
11. men must agree to use a latex condom during sexual contact with females of child bearing potential even if they have had a successful vasectomy.
Description

Gender | Latex condom Use | Vasectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C3873750
UMLS CUI [2,2]
C1524063
UMLS CUI [3]
C0042387
12. patients must have a cb unit available which is matched with the patient at 3, 4, 5, or 6/6 hla class i (serological) and ii (molecular) antigens.
Description

Umbilical Cord Blood Units Availability | Human Class I Antigens Serological | HLA class II antigen Molecular

Type de données

boolean

Alias
UMLS CUI [1,1]
C0162371
UMLS CUI [1,2]
C0439184
UMLS CUI [1,3]
C0470187
UMLS CUI [2,1]
C0008897
UMLS CUI [2,2]
C0205473
UMLS CUI [3,1]
C0312653
UMLS CUI [3,2]
C1521991
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. positive beta hcg in female of child-bearing potential defined as not postmenopausal for 24 months or no previous surgical sterilization or lactating females.
Description

Beta HCG positive | Childbearing Potential | Postmenopausal state | Female Sterilization | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0813152
UMLS CUI [2]
C3831118
UMLS CUI [3]
C0232970
UMLS CUI [4]
C0015787
UMLS CUI [5]
C0006147
2. known positive serology for hiv.
Description

HIV Seropositivity

Type de données

boolean

Alias
UMLS CUI [1]
C0019699
3. presence of grade 3 or greater toxicity from the previous treatment.
Description

Toxicity Grade Due to Prior Therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C2826262
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C1514463
4. concomitant use of other investigational agents.
Description

Investigational New Drugs Other Simultaneous

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013230
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C0521115
5. not consenting to participate in lab00-099.
Description

Laboratory Procedure Participation Unwilling

Type de données

boolean

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0558080
6. patients with known hypersensitivity to lenalidomide and/or rituximab.
Description

Hypersensitivity lenalidomide | Hypersensitivity rituximab

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1144149
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0393022
Retour au début de la page

Similar models

Eligibility Leukemia NCT02280525

1 Formulaires
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT02280525
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Chronic Lymphocytic Leukemia | Chemoimmunotherapy Standard | Persistent Disease
Item
1. patients with history of b-cll who have received at least 2 lines of standard chemoimmunotherapy and have persistent disease.
boolean
C0023434 (UMLS CUI [1])
C2986423 (UMLS CUI [2,1])
C1442989 (UMLS CUI [2,2])
C2983415 (UMLS CUI [3])
Acute lymphocytic leukemia | Leukemia, Myelocytic, Acute | Myeloid Leukemia, Chronic | Recurrent disease | Refractory Disease
Item
2. patients with acute lymphoblastic leukemia (all), acute myelogenous leukemia (aml), chronic myelogenous leukemia (cml) with relapsed or refractory disease.
boolean
C0023449 (UMLS CUI [1])
C0023467 (UMLS CUI [2])
C0023473 (UMLS CUI [3])
C0277556 (UMLS CUI [4])
C1514815 (UMLS CUI [5])
B-Cell Lymphomas | Chemotherapy Regimen | Refractory Disease | autologous hematopoietic stem cell transplant | allogenic hematopoietic stem cell transplant | rituximab | Chemotherapy Regimen Anthracyclines | Lymphoma, Follicular | Diffuse Large B-Cell Lymphoma
Item
3. patients with histologically confirmed aggressive b cell nhl with chemotherapy-refractory disease. chemotherapy refractory disease is defined as one or more of the following: stable disease or progressive disease as best response to most recent chemotherapy containing regimen or disease progression or recurrence within 12 months of prior autologous or allogeneic stem cell transplant. subjects must have received adequate prior therapy including at a minimum: anti-cd20 monoclonal antibody unless tumor is cd20-negative, an anthracycline containing chemotherapy regimen. subjects with transformed fl must have received prior chemotherapy for follicular lymphoma and subsequently have chemo-refractory disease after transformation to diffuse large b-cell lymphoma (dlbcl).
boolean
C0079731 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C1514815 (UMLS CUI [3])
C2193200 (UMLS CUI [4])
C1456094 (UMLS CUI [5])
C0393022 (UMLS CUI [6])
C0392920 (UMLS CUI [7,1])
C0282564 (UMLS CUI [7,2])
C0024301 (UMLS CUI [8])
C0079744 (UMLS CUI [9])
Hodgkin Disease | Recurrent disease | Refractory Disease
Item
4. patient with hodgkin's lymphoma with relapsed or refractory disease.
boolean
C0019829 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
C1514815 (UMLS CUI [3])
Ibrutinib | idelalisib | lenalidomide
Item
5. patients who are at least 3 weeks from the time of consent. patients may continue ibrutinib, idelalisib, or lenalidomide till the day of study consent.
boolean
C3501358 (UMLS CUI [1])
C2698692 (UMLS CUI [2])
C1144149 (UMLS CUI [3])
Karnofsky Performance Status
Item
6. karnofsky performance scale > 60%.
boolean
C0206065 (UMLS CUI [1])
Liver function | Alanine aminotransferase measurement | Serum total bilirubin measurement | Alkaline phosphatase measurement | Creatinine measurement, serum
Item
7. adequate hepatic function, as defined by sgpt <3 x upper limit of normal; serum bilirubin and alkaline phosphatase <2 x upper limit of normal, or considered not clinically significant by the study doctor or designee, serum creatinine of </=2 mg/dl.
boolean
C0232741 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C1278039 (UMLS CUI [3])
C0201850 (UMLS CUI [4])
C0201976 (UMLS CUI [5])
Informed consent
Item
8. able to provide written informed consent.
boolean
C0021430 (UMLS CUI [1])
Age
Item
9. 18-80 years of age.
boolean
C0001779 (UMLS CUI [1])
Revlimid Program | Compliance behavior | Childbearing Potential Pregnancy Test Contraceptive methods | Hysterectomy | Bilateral oophorectomy | Postmenopausal state | Menstruation
Item
10. all study participants must be registered into the mandatory revlimid remstm program, and be willing and able to comply with the requirements of the revlimid remstm program. females of childbearing potential must adhere to the scheduled pregnancy testing and contraception as required in the revlimid remstm program. a female of childbearing potential (fcbp) is a sexually mature female who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).
boolean
C1135145 (UMLS CUI [1,1])
C3484370 (UMLS CUI [1,2])
C1321605 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0032976 (UMLS CUI [3,2])
C0700589 (UMLS CUI [3,3])
C0020699 (UMLS CUI [4])
C0278321 (UMLS CUI [5])
C0232970 (UMLS CUI [6])
C0025344 (UMLS CUI [7])
Gender | Latex condom Use | Vasectomy
Item
11. men must agree to use a latex condom during sexual contact with females of child bearing potential even if they have had a successful vasectomy.
boolean
C0079399 (UMLS CUI [1])
C3873750 (UMLS CUI [2,1])
C1524063 (UMLS CUI [2,2])
C0042387 (UMLS CUI [3])
Umbilical Cord Blood Units Availability | Human Class I Antigens Serological | HLA class II antigen Molecular
Item
12. patients must have a cb unit available which is matched with the patient at 3, 4, 5, or 6/6 hla class i (serological) and ii (molecular) antigens.
boolean
C0162371 (UMLS CUI [1,1])
C0439184 (UMLS CUI [1,2])
C0470187 (UMLS CUI [1,3])
C0008897 (UMLS CUI [2,1])
C0205473 (UMLS CUI [2,2])
C0312653 (UMLS CUI [3,1])
C1521991 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Beta HCG positive | Childbearing Potential | Postmenopausal state | Female Sterilization | Breast Feeding
Item
1. positive beta hcg in female of child-bearing potential defined as not postmenopausal for 24 months or no previous surgical sterilization or lactating females.
boolean
C0813152 (UMLS CUI [1])
C3831118 (UMLS CUI [2])
C0232970 (UMLS CUI [3])
C0015787 (UMLS CUI [4])
C0006147 (UMLS CUI [5])
HIV Seropositivity
Item
2. known positive serology for hiv.
boolean
C0019699 (UMLS CUI [1])
Toxicity Grade Due to Prior Therapy
Item
3. presence of grade 3 or greater toxicity from the previous treatment.
boolean
C2826262 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C1514463 (UMLS CUI [1,3])
Investigational New Drugs Other Simultaneous
Item
4. concomitant use of other investigational agents.
boolean
C0013230 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0521115 (UMLS CUI [1,3])
Laboratory Procedure Participation Unwilling
Item
5. not consenting to participate in lab00-099.
boolean
C0022885 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
Hypersensitivity lenalidomide | Hypersensitivity rituximab
Item
6. patients with known hypersensitivity to lenalidomide and/or rituximab.
boolean
C0020517 (UMLS CUI [1,1])
C1144149 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0393022 (UMLS CUI [2,2])
Retour au début de la page 

Contact

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Aide

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