Age 18 Years to 70 Years
Item
age 18 Years to 70 Years
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Established diagnosis of CD, confirmed by standard criteria (e.g. endoscopy, ultrasound, X-ray)
Item
Established diagnosis of CD, confirmed by standard criteria (e.g. endoscopy, ultrasound, X-ray)
boolean
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0010346 (UMLS CUI 2011AA)
34000006 (SNOMED CT 2011_0131)
10011401 (MedDRA 14.1)
K50.9 (ICD-10-CM Version 2010)
C2828392 (UMLS CUI 2011AA)
CL414621 (UMLS CUI 2011AA)
C0014245 (UMLS CUI 2011AA)
423827005 (SNOMED CT 2011_0131)
10014805 (MedDRA 14.1)
MTHU008659 (LOINC Version 232)
C0041618 (UMLS CUI 2011AA)
16310003 (SNOMED CT 2011_0131)
10065594 (MedDRA 14.1)
MTHU000076 (LOINC Version 232)
12 (HL7 V3 2006_05)
C0043299 (UMLS CUI 2011AA)
363680008 (SNOMED CT 2011_0131)
87 (ICD-9-CM Version 2011)
Patients must be in clinical remission (Crohn's Disease Activity Index [CDAI] <150 points) on steroid therapy for at least 2 weeks
Item
Patients must be in clinical remission (Crohn's Disease Activity Index [CDAI] <150 points) on steroid therapy for at least 2 weeks
boolean
C0010346 (UMLS CUI 2011AA)
34000006 (SNOMED CT 2011_0131)
10011401 (MedDRA 14.1)
K50.9 (ICD-10-CM Version 2010)
C0544452 (UMLS CUI 2011AA)
277022003 (SNOMED CT 2011_0131)
C0451071 (UMLS CUI 2011AA)
273364009 (SNOMED CT 2011_0131)
C0149783 (UMLS CUI 2011AA)
297279009 (SNOMED CT 2011_0131)
10062117 (MedDRA 14.1)
Confirmed steroid-dependency of CD: patients who are either
Item
Confirmed steroid-dependency of CD: patients who are either
boolean
C0038317 (UMLS CUI 2011AA)
116566001 (SNOMED CT 2011_0131)
CL414916 (UMLS CUI 2011AA)
C0010346 (UMLS CUI 2011AA)
34000006 (SNOMED CT 2011_0131)
10011401 (MedDRA 14.1)
K50.9 (ICD-10-CM Version 2010)
unable to taper steroids completely within 3 months of starting steroids, without recurrent active disease, or
Item
unable to taper steroids completely within 3 months of starting steroids, without recurrent active disease, or
boolean
C0038317 (UMLS CUI 2011AA)
who have a relapse within 2 months of stopping steroids
Item
who have a relapse within 2 months of stopping steroids
boolean
C0277556 (UMLS CUI 2011AA)
58184002 (SNOMED CT 2011_0131)
C1947925 (UMLS CUI 2011AA)
C0038317 (UMLS CUI 2011AA)
116566001 (SNOMED CT 2011_0131)
Individual threshold dose of previous relapses should be <= 20 mg/day Prednisolone or equivalent steroid dose
Item
Individual threshold dose of previous relapses should be <= 20 mg/day Prednisolone or equivalent steroid dose
boolean
C0449864 (UMLS CUI 2011AA)
118589004 (SNOMED CT 2011_0131)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
C0205156 (UMLS CUI 2011AA)
9130008 (SNOMED CT 2011_0131)
C0277556 (UMLS CUI 2011AA)
58184002 (SNOMED CT 2011_0131)
C0032950 (UMLS CUI 2011AA)
116601002 (SNOMED CT 2011_0131)
MTHU003522 (LOINC Version 232)
CL415123 (UMLS CUI 2011AA)
Patients with stable glucocorticosteroid therapy between 20 and 40 mg/day Prednisolone or equivalent steroid dose for the previous week
Item
Patients with stable glucocorticosteroid therapy between 20 and 40 mg/day Prednisolone or equivalent steroid dose for the previous week
boolean
C0205360 (UMLS CUI 2011AA)
58158008 (SNOMED CT 2011_0131)
MTHU015276 (LOINC Version 232)
C0017710 (UMLS CUI 2011AA)
419933005 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C0032950 (UMLS CUI 2011AA)
116601002 (SNOMED CT 2011_0131)
MTHU003522 (LOINC Version 232)
CL415123 (UMLS CUI 2011AA)
Established diagnosis of UC, confirmed by standard criteria (e.g. endoscopy, ultrasound, X-ray)
Item
Established diagnosis of UC, confirmed by standard criteria (e.g. endoscopy, ultrasound, X-ray)
boolean
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0302596 (UMLS CUI 2011AA)
64766004 (SNOMED CT 2011_0131)
10009900 (MedDRA 14.1)
K51 (ICD-10-CM Version 2010)
556 (ICD-9-CM Version 2011)
C2828392 (UMLS CUI 2011AA)
CL414621 (UMLS CUI 2011AA)
C0014245 (UMLS CUI 2011AA)
423827005 (SNOMED CT 2011_0131)
10014805 (MedDRA 14.1)
MTHU008659 (LOINC Version 232)
C0041618 (UMLS CUI 2011AA)
16310003 (SNOMED CT 2011_0131)
10065594 (MedDRA 14.1)
MTHU000076 (LOINC Version 232)
12 (HL7 V3 2006_05)
C0043299 (UMLS CUI 2011AA)
363680008 (SNOMED CT 2011_0131)
87 (ICD-9-CM Version 2011)
Patients must be in clinical remission (Clinical Activity Index [CAI] <4 points) on steroid therapy for at least 2 weeks
Item
Patients must be in clinical remission (Clinical Activity Index [CAI] <4 points) on steroid therapy for at least 2 weeks
boolean
C0544452 (UMLS CUI 2011AA)
277022003 (SNOMED CT 2011_0131)
C0451071 (UMLS CUI 2011AA)
273364009 (SNOMED CT 2011_0131)
C0149783 (UMLS CUI 2011AA)
297279009 (SNOMED CT 2011_0131)
10062117 (MedDRA 14.1)
Individual threshold dose of previous relapses should be <= 20 mg/day Prednisolone or equivalent steroid dose
Item
Individual threshold dose of previous relapses should be <= 20 mg/day Prednisolone or equivalent steroid dose
boolean
C0449864 (UMLS CUI 2011AA)
118589004 (SNOMED CT 2011_0131)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
C0205156 (UMLS CUI 2011AA)
9130008 (SNOMED CT 2011_0131)
C0277556 (UMLS CUI 2011AA)
58184002 (SNOMED CT 2011_0131)
C0032950 (UMLS CUI 2011AA)
116601002 (SNOMED CT 2011_0131)
MTHU003522 (LOINC Version 232)
CL415123 (UMLS CUI 2011AA)
Patients with stable glucocorticosteroid therapy between 20 and 40 mg/day Prednisolone or equivalent steroid dose for the previous week (* The threshold dose is that dose at which the patient experienced the relapses)
Item
Patients with stable glucocorticosteroid therapy between 20 and 40 mg/day Prednisolone or equivalent steroid dose for the previous week (* The threshold dose is that dose at which the patient experienced the relapses)
boolean
C0205360 (UMLS CUI 2011AA)
58158008 (SNOMED CT 2011_0131)
MTHU015276 (LOINC Version 232)
C0017710 (UMLS CUI 2011AA)
419933005 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C0032950 (UMLS CUI 2011AA)
116601002 (SNOMED CT 2011_0131)
MTHU003522 (LOINC Version 232)
CL415123 (UMLS CUI 2011AA)
Written informed consent
Item
Written informed consent
boolean
C0021430 (UMLS CUI 2011AA)
Negative pregnancy test at screening in females of child-bearing potential
Item
Negative pregnancy test at screening in females of child-bearing potential
boolean
C0427780 (UMLS CUI 2011AA)
250425007 (SNOMED CT 2011_0131)
10036574 (MedDRA 14.1)
C1409616 (UMLS CUI 2011AA)
C0086287 (UMLS CUI 2011AA)
248152002 (SNOMED CT 2011_0131)
F (HL7 V3 2006_05)
C1148523 (UMLS CUI 2011AA)
C0237399 (UMLS CUI 2011AA)
Males willing to use condoms or to be sexually abstinent
Item
Males willing to use condoms or to be sexually abstinent
boolean
C0086582 (UMLS CUI 2011AA)
248153007 (SNOMED CT 2011_0131)
M (HL7 V3 2006_05)
C0600109 (UMLS CUI 2011AA)
225466006 (SNOMED CT 2011_0131)
C1524063 (UMLS CUI 2011AA)
260676000 (SNOMED CT 2011_0131)
C0677582 (UMLS CUI 2011AA)
C0036899 (UMLS CUI 2011AA)
47037006 (SNOMED CT 2011_0131)
10029805 (MedDRA 14.1)
Use of appropriate contraceptive methods for females of childbearing potential one month before, throughout the course of the study and one month after study termination. This must be a combination of the following:
Item
Use of appropriate contraceptive methods for females of childbearing potential one month before, throughout the course of the study and one month after study termination. This must be a combination of the following:
boolean
C0700589 (UMLS CUI 2011AA)
146680009 (SNOMED CT 2011_0131)
10010808 (MedDRA 14.1)
C0086287 (UMLS CUI 2011AA)
248152002 (SNOMED CT 2011_0131)
F (HL7 V3 2006_05)
C1148523 (UMLS CUI 2011AA)
C0237399 (UMLS CUI 2011AA)
C1947911 (UMLS CUI 2011AA)
C0332282 (UMLS CUI 2011AA)
255260001 (SNOMED CT 2011_0131)
a highly effective method of first choice = a method with a low failure rate (i.e. < 1% per year) like sexual abstinence, combined oral contraceptives, implants, injectables, some Intra Uterine Devices (IUDs), vasectomized partner together with
Item
a highly effective method of first choice = a method with a low failure rate (i.e. < 1% per year) like sexual abstinence, combined oral contraceptives, implants, injectables, some Intra Uterine Devices (IUDs), vasectomized partner together with
boolean
C0036899 (UMLS CUI 2011AA)
47037006 (SNOMED CT 2011_0131)
10029805 (MedDRA 14.1)
C0457572 (UMLS CUI 2011AA)
268458002 (SNOMED CT 2011_0131)
CL424925 (UMLS CUI 2011AA)
C1262153 (UMLS CUI 2011AA)
10062577 (MedDRA 14.1)
C0021900 (UMLS CUI 2011AA)
268460000 (SNOMED CT 2011_0131)
10022745 (MedDRA 14.1)
C0420842 (UMLS CUI 2011AA)
268457007 (SNOMED CT 2011_0131)
a method of second choice like condom, diaphragm, or cup pessary
Item
a method of second choice like condom, diaphragm, or cup pessary
boolean
C0677582 (UMLS CUI 2011AA)
C0042241 (UMLS CUI 2011AA)
20359006 (SNOMED CT 2011_0131)
C0031246 (UMLS CUI 2011AA)
46625003 (SNOMED CT 2011_0131)
Short bowel syndrome
Item
Short Bowel Syndrome
boolean
C0036992 (UMLS CUI 2011AA)
26629001 (SNOMED CT 2011_0131)
10049416 (MedDRA 14.1)
Ileostomy, colostomy or rectal pouch
Item
Ileostomy, colostomy or rectal pouch
boolean
C0020883 (UMLS CUI 2011AA)
173977007 (SNOMED CT 2011_0131)
10021321 (MedDRA 14.1)
46.20 (ICD-9-CM Version 2011)
C0009410 (UMLS CUI 2011AA)
398740003 (SNOMED CT 2011_0131)
10010041 (MedDRA 14.1)
46.10 (ICD-9-CM Version 2011)
C0939964 (UMLS CUI 2011AA)
Relapse during screening
Item
Relapse during screening
boolean
C0277556 (UMLS CUI 2011AA)
58184002 (SNOMED CT 2011_0131)
C0347984 (UMLS CUI 2011AA)
371881003 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
History of or existence of active tuberculosis
Item
History of or existence of active tuberculosis
boolean
C0375796 (UMLS CUI 2011AA)
Z86.11 (ICD-10-CM Version 2010)
V12.01 (ICD-9-CM Version 2011)
C0150312 (UMLS CUI 2011AA)
52101004 (SNOMED CT 2011_0131)
C0151332 (UMLS CUI 2011AA)
427099000 (SNOMED CT 2011_0131)
10071157 (MedDRA 14.1)
History of or existence of urolithiasis
Item
History of or existence of urolithiasis
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0150312 (UMLS CUI 2011AA)
52101004 (SNOMED CT 2011_0131)
C0451641 (UMLS CUI 2011AA)
95566004 (SNOMED CT 2011_0131)
10046707 (MedDRA 14.1)
N20-N23 (ICD-10-CM Version 2010)
History of or existence of human immune deficiency virus (HIV), Hepatitis B or C
Item
History of or existence of human immune deficiency virus (HIV), Hepatitis B or C
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0150312 (UMLS CUI 2011AA)
52101004 (SNOMED CT 2011_0131)
C0019682 (UMLS CUI 2011AA)
19030005 (SNOMED CT 2011_0131)
C0019163 (UMLS CUI 2011AA)
66071002 (SNOMED CT 2011_0131)
10019731 (MedDRA 14.1)
C0019196 (UMLS CUI 2011AA)
50711007 (SNOMED CT 2011_0131)
10019744 (MedDRA 14.1)
B19.20 (ICD-10-CM Version 2010)
070.7 (ICD-9-CM Version 2011)
C1997078 (UMLS CUI 2011AA)
429721005 (SNOMED CT 2011_0131)
History of malignancy within the past five years (excluding basal cell carcinoma of the skin)
Item
History of malignancy within the past five years (excluding basal cell carcinoma of the skin)
boolean
C2735088 (UMLS CUI 2011AA)
MTHU034770 (LOINC Version 232)
CL411789 (UMLS CUI 2011AA)
C0007117 (UMLS CUI 2011AA)
1338007 (SNOMED CT 2011_0131)
10004146 (MedDRA 14.1)
Previous opportunistic infection
Item
Previous opportunistic infection
boolean
C0205156 (UMLS CUI 2011AA)
9130008 (SNOMED CT 2011_0131)
C0029118 (UMLS CUI 2011AA)
61274003 (SNOMED CT 2011_0131)
10030901 (MedDRA 14.1)
History of serious drug sensitivity
Item
History of serious drug sensitivity
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0205404 (UMLS CUI 2011AA)
42745003 (SNOMED CT 2011_0131)
C0237865 (UMLS CUI 2011AA)
419511003 (SNOMED CT 2011_0131)
Significant cardiac arrhythmia, bradycardia or tachycardia or any other significant finding in the electrocardiogram (ECG)
Item
Significant cardiac arrhythmia, bradycardia or tachycardia or any other significant finding in the electrocardiogram (ECG)
boolean
C0003811 (UMLS CUI 2011AA)
44808001 (SNOMED CT 2011_0131)
10003119 (MedDRA 14.1)
427.9 (ICD-9-CM Version 2011)
C0428977 (UMLS CUI 2011AA)
48867003 (SNOMED CT 2011_0131)
10006093 (MedDRA 14.1)
R00.1 (ICD-10-CM Version 2010)
C0039231 (UMLS CUI 2011AA)
3424008 (SNOMED CT 2011_0131)
10019303 (MedDRA 14.1)
R00.0 (ICD-10-CM Version 2010)
785.0 (ICD-9-CM Version 2011)
C0750502 (UMLS CUI 2011AA)
386134007 (SNOMED CT 2011_0131)
CL435382 (UMLS CUI 2011AA)
C1623258 (UMLS CUI 2011AA)
46825001 (SNOMED CT 2011_0131)
10014084 (MedDRA 14.1)
Congestive heart failure
Item
Congestive heart failure, CHF
boolean
C0018802 (UMLS CUI 2011AA)
42343007 (SNOMED CT 2011_0131)
10007559 (MedDRA 14.1)
MTHU020787 (LOINC Version 232)
I50.9 (ICD-10-CM Version 2010)
428.0 (ICD-9-CM Version 2011)
Uncontrolled arterial hypertension
Item
Uncontrolled hypertension
boolean
C1868885 (UMLS CUI 2011AA)
10066860 (MedDRA 14.1)
Uncontrolled asthma
Item
Uncontrolled asthma
boolean
C0205318 (UMLS CUI 2011AA)
19032002 (SNOMED CT 2011_0131)
C0004096 (UMLS CUI 2011AA)
195967001 (SNOMED CT 2011_0131)
10003553 (MedDRA 14.1)
MTHU020815 (LOINC Version 232)
J45 (ICD-10-CM Version 2010)
493 (ICD-9-CM Version 2011)
Renal disease
Item
Kidney Disease
boolean
C0022658 (UMLS CUI 2011AA)
90708001 (SNOMED CT 2011_0131)
10029151 (MedDRA 14.1)
N18.9 (ICD-10-CM Version 2010)
Renal insufficiency defined as glomerular filtration rate (GRF) <50 ml/min/1.73 m (estimated GRF according to Cockcroft-Gault)
Item
Renal insufficiency defined as glomerular filtration rate (GRF) <50 ml/min/1.73 m (estimated GRF according to Cockcroft-Gault)
boolean
C1565489 (UMLS CUI 2011AA)
10022467 (MedDRA 14.1)
C0750572 (UMLS CUI 2011AA)
414135002 (SNOMED CT 2011_0131)
C0017654 (UMLS CUI 2011AA)
80274001 (SNOMED CT 2011_0131)
10018355 (MedDRA 14.1)
Psychiatric illness
Item
Psychiatric disorder
boolean
C0004936 (UMLS CUI 2011AA)
74732009 (SNOMED CT 2011_0131)
10037174 (MedDRA 14.1)
F99 (ICD-10-CM Version 2010)
290-319.99 (ICD-9-CM Version 2011)
Known or suspected immunodeficiency
Item
Known or suspected immunodeficiency
boolean
C0205309 (UMLS CUI 2011AA)
36692007 (SNOMED CT 2011_0131)
C0750491 (UMLS CUI 2011AA)
415684004 (SNOMED CT 2011_0131)
C0021051 (UMLS CUI 2011AA)
234532001 (SNOMED CT 2011_0131)
10061598 (MedDRA 14.1)
D84.9 (ICD-10-CM Version 2010)
279.3 (ICD-9-CM Version 2011)
Laboratory abnormalities: hemoglobin <8.5 g/dl, white blood cell count <3500/mm, platelet count <125 000/mm, clinically relevant elevation of liver enzymes, serum creatinine level >=1.4 mg/dl, hematuria (>=10 erythrocytes/field on dipsticks)
Item
Laboratory abnormalities: hemoglobin <8.5 g/dl, white blood cell count <3500/mm, platelet count <125 000/mm, clinically relevant elevation of liver enzymes, serum creatinine level >=1.4 mg/dl, hematuria (>=10 erythrocytes/field on dipsticks)
boolean
C0438215 (UMLS CUI 2011AA)
165346000 (SNOMED CT 2011_0131)
10023547 (MedDRA 14.1)
C0019046 (UMLS CUI 2011AA)
38082009 (SNOMED CT 2011_0131)
10019481 (MedDRA 14.1)
LP14449-0 (LOINC Version 232)
C0023508 (UMLS CUI 2011AA)
767002 (SNOMED CT 2011_0131)
10047939 (MedDRA 14.1)
C1287267 (UMLS CUI 2011AA)
365632008 (SNOMED CT 2011_0131)
777-3 (LOINC Version 232)
C0857093 (UMLS CUI 2011AA)
10014480 (MedDRA 14.1)
C0201976 (UMLS CUI 2011AA)
113075003 (SNOMED CT 2011_0131)
10040230 (MedDRA 14.1)
C0018965 (UMLS CUI 2011AA)
34436003 (SNOMED CT 2011_0131)
10018867 (MedDRA 14.1)
R31 (ICD-10-CM Version 2010)
599.7 (ICD-9-CM Version 2011)
E13000 (CTCAE 1105E)
Pregnancy, lactation
Item
Pregnancy, lactation
boolean
C0032961 (UMLS CUI 2011AA)
289908002 (SNOMED CT 2011_0131)
10036556 (MedDRA 14.1)
MTHU035048 (LOINC Version 232)
C0006147 (UMLS CUI 2011AA)
10006247 (MedDRA 14.1)
History of alcohol and/or drug dependence
Item
History of alcohol and/or drug dependence
boolean
C0085762 (UMLS CUI 2011AA)
Heavy smoking (> 20 cigarettes per day)
Item
Heavy smoker (over 20 per day)
boolean
C0337669 (UMLS CUI 2011AA)
56771006 (SNOMED CT 2011_0131)
Use of prohibited drugs or treatments
Item
Use of prohibited drugs or treatments
boolean
C1524063 (UMLS CUI 2011AA)
260676000 (SNOMED CT 2011_0131)
C0683610 (UMLS CUI 2011AA)
C0013227 (UMLS CUI 2011AA)
C0039798 (UMLS CUI 2011AA)
Patient not able or not willing to follow study procedures due to physical or psychological limitations or language problems
Item
Patient not able or not willing to follow study procedures due to physical or psychological limitations or language problems
boolean
C0457432 (UMLS CUI 2011AA)
258143003 (SNOMED CT 2011_0131)
C0680734 (UMLS CUI 2011AA)
CL420107 (UMLS CUI 2011AA)
C0520817 (UMLS CUI 2011AA)
32572006 (SNOMED CT 2011_0131)
10048624 (MedDRA 14.1)
C1306341 (UMLS CUI 2011AA)
47437004 (SNOMED CT 2011_0131)
10027374 (MedDRA 14.1)
F79 (ICD-10-CM Version 2010)
C0023015 (UMLS CUI 2011AA)
62305002 (SNOMED CT 2011_0131)
F80.9 (ICD-10-CM Version 2010)
Participation in another investigational drug or vaccine trial within the last three months or concurrently with this study
Item
Participation in another investigational drug or vaccine trial within the last three months or concurrently with this study
boolean
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0013230 (UMLS CUI 2011AA)
C0042210 (UMLS CUI 2011AA)
71181003 (SNOMED CT 2011_0131)
MTHU014526 (LOINC Version 232)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
Vaccination with life attenuated viruses within 4 weeks prior to study start
Item
Vaccination with life attenuated viruses within 4 weeks prior to study start
boolean
C0042196 (UMLS CUI 2011AA)
33879002 (SNOMED CT 2011_0131)
10046859 (MedDRA 14.1)
MTHU000146 (LOINC Version 232)
C1516086 (UMLS CUI 2011AA)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C2348558 (UMLS CUI 2011AA)
Patient with any medical condition which, in the opinion of the investigator or his designee, could jeopardize or compromise the ability of the patient to participate in the trial
Item
Patient with any medical condition which, in the opinion of the investigator or his designee, could jeopardize or compromise the ability of the patient to participate in the trial
boolean
C1699700 (UMLS CUI 2011AA)
MEDCCAT (HL7 V3 2006_05)
C0221099 (UMLS CUI 2011AA)
260379002 (SNOMED CT 2011_0131)
C0085732 (UMLS CUI 2011AA)
371150009 (SNOMED CT 2011_0131)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
Patients possibly dependent on the investigator or the sponsor
Item
Patients possibly dependent on the investigator or the sponsor
boolean
C0030705 (UMLS CUI 2011AA)
116154003 (SNOMED CT 2011_0131)
CL414916 (UMLS CUI 2011AA)
CL102947 (UMLS CUI 2011AA)
C2347796 (UMLS CUI 2011AA)