ID

12213

Beschreibung

Study of Efficacy and Safety of LJM716 and Cetuximab in Head and Neck Squamous Cell Carcinoma Patients; ODM derived from: https://clinicaltrials.gov/show/NCT02143622

Link

https://clinicaltrials.gov/show/NCT02143622

Stichworte

  1. 18.10.15 18.10.15 -
Hochgeladen am

18. Oktober 2015

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Head and Neck Squamous Cell Carcinoma NCT02143622

Eligibility Head and Neck Squamous Cell Carcinoma NCT02143622

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
most recent regimen contains both platinum and cetuximab (phase ii, group b).
Beschreibung

cetuximab; platinum

Datentyp

boolean

Alias
UMLS CUI [1]
C0995188
UMLS CUI [2]
C0032207
ecog performance status (ps) ≤ 2.
Beschreibung

ecog performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
recovery from all aes of previous anti-cancer therapies, to baseline or to ctcae grade ≤ 1, except for alopecia.
Beschreibung

Antineoplastic Drug/Agent Therapy

Datentyp

boolean

Alias
UMLS CUI [1]
C2346834
measurable disease as determined by recist v1.1.
Beschreibung

measurable disease

Datentyp

boolean

Alias
UMLS CUI [1]
C1513041
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous anti-her3 antibody treatment.
Beschreibung

treatment specific antibody

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0443640
symptomatic brain metastasis.
Beschreibung

symptomatic; metastasis; brain

Datentyp

boolean

Alias
UMLS CUI [1]
C0231220
UMLS CUI [2]
C0027627
UMLS CUI [3]
C0006104
prior systemic anti-cancer treatment, within a period of time that is shorter than the cycle length used for that treatment prior to starting study treatment.
Beschreibung

cancer treatment; systemic

Datentyp

boolean

Alias
UMLS CUI [1]
C0920425
UMLS CUI [2]
C0205373
prior anaphylactic or other severe infusion reaction to human immunoglobulin or antibody formulations.
Beschreibung

allergy human immunoglobulin

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C3537193
inadequate end organ function.
Beschreibung

Organ or Tissue Function

Datentyp

boolean

Alias
UMLS CUI [1]
C1254358
ongoing diarrhea ctcae grade ≥ 2. other protocol-defined inclusion/exclusion criteria may apply
Beschreibung

diarrhea

Datentyp

boolean

Alias
UMLS CUI [1]
C0011991

Ähnliche Modelle

Eligibility Head and Neck Squamous Cell Carcinoma NCT02143622

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
cetuximab; platinum
Item
most recent regimen contains both platinum and cetuximab (phase ii, group b).
boolean
C0995188 (UMLS CUI [1])
C0032207 (UMLS CUI [2])
ecog performance status
Item
ecog performance status (ps) ≤ 2.
boolean
C1520224 (UMLS CUI [1])
Antineoplastic Drug/Agent Therapy
Item
recovery from all aes of previous anti-cancer therapies, to baseline or to ctcae grade ≤ 1, except for alopecia.
boolean
C2346834 (UMLS CUI [1])
measurable disease
Item
measurable disease as determined by recist v1.1.
boolean
C1513041 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
treatment specific antibody
Item
previous anti-her3 antibody treatment.
boolean
C0087111 (UMLS CUI [1,1])
C0443640 (UMLS CUI [1,2])
symptomatic; metastasis; brain
Item
symptomatic brain metastasis.
boolean
C0231220 (UMLS CUI [1])
C0027627 (UMLS CUI [2])
C0006104 (UMLS CUI [3])
cancer treatment; systemic
Item
prior systemic anti-cancer treatment, within a period of time that is shorter than the cycle length used for that treatment prior to starting study treatment.
boolean
C0920425 (UMLS CUI [1])
C0205373 (UMLS CUI [2])
allergy human immunoglobulin
Item
prior anaphylactic or other severe infusion reaction to human immunoglobulin or antibody formulations.
boolean
C0020517 (UMLS CUI [1,1])
C3537193 (UMLS CUI [1,2])
Organ or Tissue Function
Item
inadequate end organ function.
boolean
C1254358 (UMLS CUI [1])
diarrhea
Item
ongoing diarrhea ctcae grade ≥ 2. other protocol-defined inclusion/exclusion criteria may apply
boolean
C0011991 (UMLS CUI [1])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video