ID

17654

Beskrivning

Sponsor: OSI Pharmaceuticals Information provided by (Responsible Party): Astellas Pharma Inc (OSI Pharmaceuticals) A multicenter, randomized, double-blind, placebo-controlled, phase 3 study of single-agent Tarceva® (erlotinib) following complete tumor resection with or without adjuvant chemotherapy in patients with stage IB-IIIA non-small cell lung carcinoma who have EGFR-positive tumors. See https://clinicaltrials.gov/ct2/show/NCT00373425 Part of study: Open-label Tarceva Consent and Eligibility

Länk

https://clinicaltrials.gov/ct2/show/NCT00373425

Nyckelord

Versioner (2)
  1. 2016-08-02 2016-08-02 -
  2. 2016-09-27 2016-09-27 -
Uppladdad den

27 september 2016

DOI

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Licens

Creative Commons BY 4.0
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Open-label Tarceva, Tarceva in NSCLC patients who have EGFR-positive tumors DRKS00001485 NCT00373425

Engelsk

Open-label Tarceva Consent and Eligibility, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

1 Formulär  
Open Label Tarceva Consent
Beskrivning

Open Label Tarceva Consent

Date addendum to main study consent was signed:
Beskrivning

Consent date

Datatyp

date

Alias
UMLS CUI [1]
C2985782
Open-label Tarceva: please check one
Beskrivning

Open-label Tarceva

Datatyp

integer

Alias
UMLS CUI [1,1]
C1709323
UMLS CUI [1,2]
C1135136
Open-label Tarceva Eligibility
Beskrivning

Open-label Tarceva Eligibility

Open-label Tarceva Eligibility: Not Applicable
Beskrivning

Open-label Tarceva Eligibility

Datatyp

boolean

Alias
UMLS CUI [1]
C1516637
Did the patient meet all of the eligibility criteria to receive open-label Tarceva?
Beskrivning

Eligibility Criteria: OSI-774-302 Protocol Version 2, 21 November 2007, Appendix 12.9

Datatyp

boolean

Alias
UMLS CUI [1]
C1302261
If No, which of the 4 criteria was/were not met? Criteria 1 met?
Beskrivning

Eligibility Criteria

Datatyp

boolean

Alias
UMLS CUI [1]
C1516637
If No, which of the 4 criteria was/were not met? Criteria 2 met?
Beskrivning

Eligibility Criteria

Datatyp

boolean

Alias
UMLS CUI [1]
C1516637
If No, which of the 4 criteria was/were not met? Criteria 3 met?
Beskrivning

Eligibility Criteria

Datatyp

boolean

Alias
UMLS CUI [1]
C1516637
If No, which of the 4 criteria was/were not met? Criteria 4 met?
Beskrivning

Eligibility Criteria

Datatyp

boolean

Alias
UMLS CUI [1]
C1516637
lf any eligibility criteria were not met, was an exemption granted by OSI?
Beskrivning

Exemption

Datatyp

integer

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C2348482
Investigator Signature
Beskrivning

Investigator Signature

Investigator's Signature:
Beskrivning

I have reviewed all data for this patient's eligibility and confirm that consent has been obtained in accordance with the GCP Directive (2005/28/EC) or EU Directive (2001/20/EC) and other applicable GCP requirements.

Datatyp

text

Alias
UMLS CUI [1]
C2346576
Date
Beskrivning

Investigator Signature Date

Datatyp

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008
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Similar models

Open-label Tarceva Consent and Eligibility, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Open Label Tarceva Consent
Consent date
Item
Date addendum to main study consent was signed:
date
C2985782 (UMLS CUI [1])
Item
Open-label Tarceva: please check one
integer
C1709323 (UMLS CUI [1,1])
C1135136 (UMLS CUI [1,2])
Open-label Tarceva
Code List
Open-label Tarceva: please check one
CL Item
Patient to receive open-label Tarceva for up to two years and will be followed for all On-treatment, Post-treatment and Long-term Follow-up Assessments according to the protocol. (Complete Open-label Baseline Assessments.) (1)
CL Item
Patient not to receive open-label Tarceva but will remain in the study and continue to be followed for all Post-treatment and Long-term Follow-up Assessments. (Complete Post-treatment Assessments and Long-term Follow-up Assessments.) (2)
Item Group
Open-label Tarceva Eligibility
Open-label Tarceva Eligibility
Item
Open-label Tarceva Eligibility: Not Applicable
boolean
C1516637 (UMLS CUI [1])
Eligibility
Item
Did the patient meet all of the eligibility criteria to receive open-label Tarceva?
boolean
C1302261 (UMLS CUI [1])
Eligibility Criteria
Item
If No, which of the 4 criteria was/were not met? Criteria 1 met?
boolean
C1516637 (UMLS CUI [1])
Eligibility Criteria
Item
If No, which of the 4 criteria was/were not met? Criteria 2 met?
boolean
C1516637 (UMLS CUI [1])
Eligibility Criteria
Item
If No, which of the 4 criteria was/were not met? Criteria 3 met?
boolean
C1516637 (UMLS CUI [1])
Eligibility Criteria
Item
If No, which of the 4 criteria was/were not met? Criteria 4 met?
boolean
C1516637 (UMLS CUI [1])
Item
lf any eligibility criteria were not met, was an exemption granted by OSI?
integer
C1516637 (UMLS CUI [1,1])
C2348482 (UMLS CUI [1,2])
Exemption
Code List
lf any eligibility criteria were not met, was an exemption granted by OSI?
CL Item
Yes (1)
CL Item
No (2)
CL Item
NA (3)
Item Group
Investigator Signature
Investigator Signature
Item
Investigator's Signature:
text
C2346576 (UMLS CUI [1])
Investigator Signature Date
Item
Date
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Tillbaka till toppen 

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