ID
41199
Description
Study to Evaluate the Safety and Tolerability of Weekly Intravenous (IV) Doses of BMS-906024 in Subjects With Acute T-cell Lymphoblastic Leukemia or T-cell Lymphoblastic Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT01363817
Link
https://clinicaltrials.gov/show/NCT01363817
Keywords
Versions (1)
- 7/11/20 7/11/20 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
July 11, 2020
DOI
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License
Creative Commons BY 4.0
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Eligibility Lymphoblastic Leukemia, Acute T-cell NCT01363817
Eligibility Lymphoblastic Leukemia, Acute T-cell NCT01363817
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Communicable Disease
Data type
boolean
Alias
- UMLS CUI [1]
- C0009450
Description
Triglyceride increased
Data type
boolean
Alias
- UMLS CUI [1]
- C5200999
Description
Gastrointestinal Disease | High risk of Diarrhea | Inflammatory Bowel Diseases
Data type
boolean
Alias
- UMLS CUI [1]
- C0017178
- UMLS CUI [2,1]
- C0332167
- UMLS CUI [2,2]
- C0011991
- UMLS CUI [3]
- C0021390
Description
Bone marrow biopsy Receive Unable
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0005954
- UMLS CUI [1,2]
- C1514756
- UMLS CUI [1,3]
- C1299582
Description
Pharmaceutical Preparations At risk Torsades de Pointes
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1444641
- UMLS CUI [1,3]
- C0040479
Similar models
Eligibility Lymphoblastic Leukemia, Acute T-cell NCT01363817
- StudyEvent: Eligibility
C1335731 (UMLS CUI [2])
C1504525 (UMLS CUI [3])
C0862284 (UMLS CUI [4])
C0231290 (UMLS CUI [5,1])
C2936643 (UMLS CUI [5,2])
C0205156 (UMLS CUI [1,2])
C0243161 (UMLS CUI [2,1])
C1550543 (UMLS CUI [2,2])
C0332167 (UMLS CUI [2,1])
C0011991 (UMLS CUI [2,2])
C0021390 (UMLS CUI [3])
C1514756 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C1444641 (UMLS CUI [1,2])
C0040479 (UMLS CUI [1,3])