ID

30369

Description

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

Lien

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

Mots-clés

  1. 30/05/2018 30/05/2018 - Halim Ugurlu
Détendeur de droits

GlaxoSmithKline (GSK)

Téléchargé le

30 mai 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

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

Blood Products and Blood Supportive Care Products, Paclitaxel Premedications

Blood Products and Blood Supportive Care Products
Description

Blood Products and Blood Supportive Care Products

Alias
UMLS CUI-1
C0456388
Blood Products and Blood Supportive Care Products
Description

Blood Products and Blood Supportive Care Products

Type de données

integer

Alias
UMLS CUI [1,1]
C0456388
UMLS CUI [1,2]
C0371802
Cumulative Quantity or Dose
Description

Cumulative Quantity or Dose

Type de données

text

Alias
UMLS CUI [1,1]
C2986497
UMLS CUI [1,2]
C1521826
Units
Description

Units

Type de données

text

Alias
UMLS CUI [1,1]
C0450442
UMLS CUI [1,2]
C1519795
Start Date
Description

Start Date

Type de données

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Description

Stop Date

Type de données

date

Alias
UMLS CUI [1]
C0806020
Paclitaxel Premedications
Description

Paclitaxel Premedications

Alias
UMLS CUI-1
C0144576
UMLS CUI-2
C0033045
Drug name
Description

Trade name preferred

Type de données

text

Alias
UMLS CUI [1]
C2360065
Total Daily Dose
Description

Total Daily Dose

Type de données

text

Alias
UMLS CUI [1]
C2348070
Units
Description

Units

Type de données

text

Alias
UMLS CUI [1,1]
C0450442
UMLS CUI [1,2]
C1519795
Start Date
Description

Start Date

Type de données

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Description

Stop Date

Type de données

date

Alias
UMLS CUI [1]
C0806020

Similar models

Blood Products and Blood Supportive Care Products, Paclitaxel Premedications

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Blood Products and Blood Supportive Care Products
C0456388 (UMLS CUI-1)
Item
Blood Products and Blood Supportive Care Products
integer
C0456388 (UMLS CUI [1,1])
C0371802 (UMLS CUI [1,2])
Code List
Blood Products and Blood Supportive Care Products
CL Item
Red Blood Cells (1)
CL Item
Platelets (2)
CL Item
Whole Blood (3)
CL Item
Plasma - FFP (4)
CL Item
Factor VIII (5)
CL Item
Cryoprecipitate (6)
CL Item
White Blood Cells (7)
CL Item
Other Blood Product (8)
CL Item
G-CSF (9)
CL Item
Prophylactic G-CSF (10)
CL Item
Treatment G-CSF (11)
CL Item
G(M)CSF (12)
CL Item
Erythropoietin (13)
CL Item
Pegfilgrastim (Conjugated G-CSF/Neulasta) (14)
CL Item
Oprelvecin (IL-11) (15)
CL Item
Other Blood Supportive Care Product, specify (16)
Cumulative Quantity or Dose
Item
Cumulative Quantity or Dose
text
C2986497 (UMLS CUI [1,1])
C1521826 (UMLS CUI [1,2])
Units
Item
Units
text
C0450442 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])
Item Group
Paclitaxel Premedications
C0144576 (UMLS CUI-1)
C0033045 (UMLS CUI-2)
Drug name
Item
Drug name
text
C2360065 (UMLS CUI [1])
Total Daily Dose
Item
Total Daily Dose
text
C2348070 (UMLS CUI [1])
Units
Item
Units
text
C0450442 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial