ID
17653
Description
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: Withdrawal of Consent
Link
https://clinicaltrials.gov/ct2/show/NCT00373425
Keywords
Versions (2)
- 8/2/16 8/2/16 -
- 9/27/16 9/27/16 -
Uploaded on
September 27, 2016
DOI
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License
Creative Commons BY 4.0
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Withdrawal of Consent, Tarceva in NSCLC patients who have EGFR-positive tumors DRKS00001485 NCT00373425
Withdrawal of Consent, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425
Description
Withdrawal of Tissue Consent
Description
Withdrawal of Tissue Consent
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0475358
Description
Date Consent Withdrawn
Data type
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0011008
Description
Withdrawal of Optional Research Blood Sample Consent
Description
Withdrawal of Optional Research Blood Sample Consent
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0178913
Description
Date Consent Withdrawn
Data type
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0011008
Description
Investigator Signature
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Withdrawal of Consent, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425
C0087111 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0475358 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])