ID
35190
Beschrijving
A Phase 1, Dose-Escalation Trial of PT2385 Tablets In Patients With Advanced Clear Cell Renal Cell Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT02293980
Link
https://clinicaltrials.gov/show/NCT02293980
Trefwoorden
Versies (1)
- 23-02-19 23-02-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
23 februari 2019
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility ccRCC NCT02293980
Eligibility ccRCC NCT02293980
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Metastatic malignant neoplasm to brain Untreated | Leptomeningeal disease | Compression of spinal cord
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0220650
- UMLS CUI [1,2]
- C0332155
- UMLS CUI [2]
- C0751297
- UMLS CUI [3]
- C0037926
Beschrijving
Effect Reversible Due to Cancer treatment | Recovery failed
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1280500
- UMLS CUI [1,2]
- C0205343
- UMLS CUI [1,3]
- C0678226
- UMLS CUI [1,4]
- C0920425
- UMLS CUI [2,1]
- C2004454
- UMLS CUI [2,2]
- C0231175
Beschrijving
Uncontrolled hypertension | Poor hypertension control
Datatype
boolean
Alias
- UMLS CUI [1]
- C1868885
- UMLS CUI [2]
- C0421190
Beschrijving
Warfarin | Anticoagulant therapy | Requirement Warfarin Expected
Datatype
boolean
Alias
- UMLS CUI [1]
- C0043031
- UMLS CUI [2]
- C0150457
- UMLS CUI [3,1]
- C1514873
- UMLS CUI [3,2]
- C0043031
- UMLS CUI [3,3]
- C1517001
Beschrijving
Cardiovascular event Major
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1320716
- UMLS CUI [1,2]
- C0205164
Beschrijving
Heart Disease | Respiration Disorder | Other medical condition Interferes with Study Subject Participation Status | Mental condition Interferes with Study Subject Participation Status | Other medical condition Interferes with Interpretation Research results | Mental condition Interferes with Interpretation Research results
Datatype
boolean
Alias
- UMLS CUI [1]
- C0018799
- UMLS CUI [2]
- C0035204
- UMLS CUI [3,1]
- C3843040
- UMLS CUI [3,2]
- C0521102
- UMLS CUI [3,3]
- C2348568
- UMLS CUI [4,1]
- C3840291
- UMLS CUI [4,2]
- C0521102
- UMLS CUI [4,3]
- C2348568
- UMLS CUI [5,1]
- C3843040
- UMLS CUI [5,2]
- C0521102
- UMLS CUI [5,3]
- C0459471
- UMLS CUI [5,4]
- C0683954
- UMLS CUI [6,1]
- C3840291
- UMLS CUI [6,2]
- C0521102
- UMLS CUI [6,3]
- C0459471
- UMLS CUI [6,4]
- C0683954
Beschrijving
Major surgery
Datatype
boolean
Alias
- UMLS CUI [1]
- C0679637
Beschrijving
HIV Infection
Datatype
boolean
Alias
- UMLS CUI [1]
- C0019693
Beschrijving
Communicable Disease Requirement Systemic therapy
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0009450
- UMLS CUI [1,2]
- C1514873
- UMLS CUI [1,3]
- C1515119
Beschrijving
Study Subject Participation Status
Datatype
boolean
Alias
- UMLS CUI [1]
- C2348568
Similar models
Eligibility ccRCC NCT02293980
- StudyEvent: Eligibility
C0205179 (UMLS CUI [1,2])
C1517927 (UMLS CUI [1,3])
C2931852 (UMLS CUI [2])
C0242656 (UMLS CUI [3])
C1514463 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C0232970 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0079399 (UMLS CUI [4,1])
C0682323 (UMLS CUI [4,2])
C0086287 (UMLS CUI [4,3])
C0700589 (UMLS CUI [4,4])
C0175795 (UMLS CUI [1,2])
C0332155 (UMLS CUI [1,2])
C0751297 (UMLS CUI [2])
C0037926 (UMLS CUI [3])
C0205343 (UMLS CUI [1,2])
C0678226 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0231175 (UMLS CUI [2,2])
C0421190 (UMLS CUI [2])
C0150457 (UMLS CUI [2])
C1514873 (UMLS CUI [3,1])
C0043031 (UMLS CUI [3,2])
C1517001 (UMLS CUI [3,3])
C0205164 (UMLS CUI [1,2])
C0035204 (UMLS CUI [2])
C3843040 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C2348568 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C2348568 (UMLS CUI [4,3])
C3843040 (UMLS CUI [5,1])
C0521102 (UMLS CUI [5,2])
C0459471 (UMLS CUI [5,3])
C0683954 (UMLS CUI [5,4])
C3840291 (UMLS CUI [6,1])
C0521102 (UMLS CUI [6,2])
C0459471 (UMLS CUI [6,3])
C0683954 (UMLS CUI [6,4])
C1514873 (UMLS CUI [1,2])
C1515119 (UMLS CUI [1,3])