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ID

16730

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 of study: Concomitant Medications

Lien

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

Mots-clés

  1. 02/08/2016 02/08/2016 -
  2. 03/08/2016 03/08/2016 - Julian Varghese
Téléchargé le

3 août 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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    Concomitant Medications, Tarceva in NSCLC patients who have EGFR-positive tumors DRKS00001485 NCT00373425

    Concomitant Medications, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

    Concomitant Medications
    Description

    Concomitant Medications

    Concomitant Medication
    Description

    Concomitant Medication

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    Medications
    Description

    Medications

    Medication (Use generic name when possible)
    Description

    Concomitant Medication

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2347852
    Prophylaxis
    Description

    Indication Prophylaxis

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C2826696
    UMLS CUI [1,2]
    C0199176
    Indication
    Description

    Indication

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2826696
    Date started: Prestudy
    Description

    Concomitant Medication Start Date

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2826734
    Date started
    Description

    Concomitant Medication Start Date

    Type de données

    date

    Alias
    UMLS CUI [1]
    C2826734
    Date stopped: Post treatment
    Description

    Concomitant Medication End Date

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2826744
    Date stopped
    Description

    Concomitant Medication End Date

    Type de données

    date

    Alias
    UMLS CUI [1]
    C2826744

    Similar models

    Concomitant Medications, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Concomitant Medications
    Concomitant Medication
    Item
    Concomitant Medication
    boolean
    C2347852 (UMLS CUI [1])
    Item Group
    Medications
    Concomitant Medication
    Item
    Medication (Use generic name when possible)
    text
    C2347852 (UMLS CUI [1])
    Indication Prophylaxis
    Item
    Prophylaxis
    boolean
    C2826696 (UMLS CUI [1,1])
    C0199176 (UMLS CUI [1,2])
    Indication
    Item
    Indication
    text
    C2826696 (UMLS CUI [1])
    Concomitant Medication Start Date
    Item
    Date started: Prestudy
    boolean
    C2826734 (UMLS CUI [1])
    Concomitant Medication Start Date
    Item
    Date started
    date
    C2826734 (UMLS CUI [1])
    Concomitant Medication End Date
    Item
    Date stopped: Post treatment
    boolean
    C2826744 (UMLS CUI [1])
    Concomitant Medication End Date
    Item
    Date stopped
    date
    C2826744 (UMLS CUI [1])

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