ID

30324

Beschrijving

https://clinicaltrials.gov/ct2/show/NCT00486954 Study ID: 104578 Clinical Study ID: EGF104578 Study Title: A Randomized, Multicenter, Open-label, Phase III Study of Lapatinib (GW572016) in Combination with weekly Paclitaxel versus weekly Paclitaxel alone in the second line treatment of ErbB2 amplified Advanced Gastric Cancer Patient Level Data: Clinicaltrials.gov Identifier: NCT00486954 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Product Sponsorship Transferred to Novartis Generic Name: lapatinib Trade Name: Tyverb,Tykerb,Tycerb Study Indication: Neoplasms, Gastrointestinal Tract CRF Seiten: 1288-1609

Link

https://clinicaltrials.gov/ct2/show/NCT00486954

Trefwoorden

  1. 29-05-18 29-05-18 - Halim Ugurlu
Houder van rechten

GlaxoSmithKline (GSK)

Geüploaded op

29 mei 2018

DOI

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Licentie

Creative Commons BY-NC 3.0

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NCT00486954_Lapatinib in Combination With Weekly Paclitaxel in Patients With ErbB2 Amplified Advanced Gastric Cancer

Dose-Limiting Toxicity

  1. StudyEvent: ODM
    1. Dose-Limiting Toxicity
Dose Limiting Toxicity
Beschrijving

Dose Limiting Toxicity

Alias
UMLS CUI-1
C1512043
UMLS CUI-2
C0013221
Did the subject experience a dose-limiting toxicity?
Beschrijving

Dose Limiting Toxicity

Datatype

boolean

Alias
UMLS CUI [1,1]
C1512043
UMLS CUI [1,2]
C0013221
If yes to Dose Limiting Toxicity, specify the toxicities and onset dates below and record details in the Non-Serious Adverse Events or Serious Adverse Events sections.
Beschrijving

If yes to Dose Limiting Toxicity

Datatype

text

Alias
UMLS CUI [1,1]
C1512043
UMLS CUI [1,2]
C0013221

Similar models

Dose-Limiting Toxicity

  1. StudyEvent: ODM
    1. Dose-Limiting Toxicity
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Dose Limiting Toxicity
C1512043 (UMLS CUI-1)
C0013221 (UMLS CUI-2)
Dose Limiting Toxicity
Item
Did the subject experience a dose-limiting toxicity?
boolean
C1512043 (UMLS CUI [1,1])
C0013221 (UMLS CUI [1,2])
If yes to Dose Limiting Toxicity
Item
If yes to Dose Limiting Toxicity, specify the toxicities and onset dates below and record details in the Non-Serious Adverse Events or Serious Adverse Events sections.
text
C1512043 (UMLS CUI [1,1])
C0013221 (UMLS CUI [1,2])

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