ID

34479

Beskrivning

Bioavailability Study of ODM-201 in Subjects With Metastatic Chemotherapy-naive Castration-resistant Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01784757

Länk

https://clinicaltrials.gov/show/NCT01784757

Nyckelord

  1. 2019-01-17 2019-01-17 -
  2. 2019-05-22 2019-05-22 -
Rättsinnehavare

GSK group of companies

Uppladdad den

17 januari 2019

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Prostate Cancer NCT01784757

Eligibility Prostate Cancer NCT01784757

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
written informed consent (ic) obtained.
Beskrivning

ID.1

Datatyp

boolean

histologically confirmed adenocarcinoma of prostate
Beskrivning

ID.2

Datatyp

boolean

progressive metastatic disease
Beskrivning

ID.3

Datatyp

boolean

ongoing androgen deprivation therapy with a luteinising hormone-releasing hormone (lhrh) analogue or antagonist or bilateral orchiectomy
Beskrivning

ID.4

Datatyp

boolean

adequate bone marrow, hepatic and renal function
Beskrivning

ID.5

Datatyp

boolean

able to swallow the odm-201 whole as a capsule or tablet.
Beskrivning

ID.6

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous chemotherapy for prostate cancer.
Beskrivning

ID.7

Datatyp

boolean

known metastases in the brain.
Beskrivning

ID.8

Datatyp

boolean

history of other malignancy within the previous 5 years, except a basal cell carcinoma of skin.
Beskrivning

ID.9

Datatyp

boolean

known gastrointestinal condition that can significantly affect the absorption of the study treatment.
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Prostate Cancer NCT01784757

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
written informed consent (ic) obtained.
boolean
ID.2
Item
histologically confirmed adenocarcinoma of prostate
boolean
ID.3
Item
progressive metastatic disease
boolean
ID.4
Item
ongoing androgen deprivation therapy with a luteinising hormone-releasing hormone (lhrh) analogue or antagonist or bilateral orchiectomy
boolean
ID.5
Item
adequate bone marrow, hepatic and renal function
boolean
ID.6
Item
able to swallow the odm-201 whole as a capsule or tablet.
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
previous chemotherapy for prostate cancer.
boolean
ID.8
Item
known metastases in the brain.
boolean
ID.9
Item
history of other malignancy within the previous 5 years, except a basal cell carcinoma of skin.
boolean
ID.10
Item
known gastrointestinal condition that can significantly affect the absorption of the study treatment.
boolean

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