ID

20211

Beschrijving

This study is a prospective, interventional, open-label, multi-center early access program for the use of Ra-223 Cl2 in HRPC/CRPC (Hormone refractory prostate cancer / Castrate resistant prostate cancer) patients diagnosed with bone metastasis and to collect additional short and long term safety data on the product. NCT01618370

Trefwoorden

  1. 13-02-17 13-02-17 -
Geüploaded op

13 februari 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Radium-223 Dichloride (Alpharadin) DRKS00006460 NCT01618370 in Castration-Resistant (Hormone-Refractory) Prostate Cancer Patients With Bone Metastases (Prior Therapy)

Radium 223 Dichloride (Alpharadin) - Prior Anti-Cancer Therapy

Prior systemic Anti-Cancer Therapy
Beschrijving

Prior systemic Anti-Cancer Therapy

Has the subject received any prior systemic anti-cancer therapy?
Beschrijving

May include chemotherapy,hormonal therapy, immunotherapy and non-conventional therapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C2346834
UMLS CUI [1,2]
C1514463
Regimen number
Beschrijving

Regimen number

Datatype

text

Alias
UMLS CUI [1,1]
C0040808
UMLS CUI [1,2]
C0237753
Intent
Beschrijving

Intent

Datatype

text

Alias
UMLS CUI [1,1]
C1283828
UMLS CUI [1,2]
C2346834
Type
Beschrijving

Type of treatment

Datatype

text

Alias
UMLS CUI [1]
C0087111
Drug name (Trade Name preferred)
Beschrijving

Use trade name where possible

Datatype

text

Alias
UMLS CUI [1]
C0013227
Start Date
Beschrijving

Start Date

Datatype

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Beschrijving

Stop Date

Datatype

date

Alias
UMLS CUI [1]
C0806020

Similar models

Radium 223 Dichloride (Alpharadin) - Prior Anti-Cancer Therapy

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Prior systemic Anti-Cancer Therapy
Prior systemic anti-cancer therapy
Item
Has the subject received any prior systemic anti-cancer therapy?
boolean
C2346834 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
Regimen number
Item
Regimen number
text
C0040808 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Intent
Item
Intent
text
C1283828 (UMLS CUI [1,1])
C2346834 (UMLS CUI [1,2])
Type of treatment
Item
Type
text
C0087111 (UMLS CUI [1])
Drug name
Item
Drug name (Trade Name preferred)
text
C0013227 (UMLS CUI [1])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])

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