ID

34288

Descrição

Investigation on Safety, Tolerability, and Pharmacokinetics of Single Doses of NNC0113-0987 in Healthy Male Subjects; ODM derived from: https://clinicaltrials.gov/show/NCT01690169

Link

https://clinicaltrials.gov/show/NCT01690169

Palavras-chave

  1. 16/01/2019 16/01/2019 -
Titular dos direitos

GSK group of companies

Transferido a

16 de janeiro de 2019

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Diabetes NCT01690169

Eligibility Diabetes NCT01690169

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01690169
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
male subjects with good general health as judged by the investigator, based on medical history, physical examination including 12-lead electrocardiogram (ecg), vital signs, and blood assessments at the screening visit
Descrição

ID.1

Tipo de dados

boolean

body mass index (bmi) above or equal to 18.5 and below 30 kg/m^ 2
Descrição

ID.2

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
male subjects who are sexually active and not surgically sterilised, who or whose partner is unwilling to use two different forms of effective contraception, one of which has to be a barrier method (e.g., condom with spermicidal foam/gel/film/cream) for the duration of the trial and for 12 weeks following the last dose of trial medication
Descrição

ID.3

Tipo de dados

boolean

participation in another trial within 90 days prior to screening
Descrição

ID.4

Tipo de dados

boolean

subjects with a history of or presence of cancer, diabetes, or any clinically significant cardiovascular, respiratory, metabolic, renal, hepatic, gastrointestinal (including gastroesophageal reflux disease and irritable bowel syndrome), endocrinological, haematological, dermatological, venereal, neurological, or psychiatric disease or other major disorders that might have an impact on the current trial, as judged by the investigator
Descrição

ID.5

Tipo de dados

boolean

subjects who are known to have hepatitis or who are carriers of the hepatitis b surface antigen (hbsag) or hepatitis c antibodies, or have a positive result to the test for human immunodeficiency virus (hiv) antibodies
Descrição

ID.6

Tipo de dados

boolean

history of acute idiopathic or chronic pancreatitis
Descrição

ID.7

Tipo de dados

boolean

Similar models

Eligibility Diabetes NCT01690169

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01690169
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
male subjects with good general health as judged by the investigator, based on medical history, physical examination including 12-lead electrocardiogram (ecg), vital signs, and blood assessments at the screening visit
boolean
ID.2
Item
body mass index (bmi) above or equal to 18.5 and below 30 kg/m^ 2
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
male subjects who are sexually active and not surgically sterilised, who or whose partner is unwilling to use two different forms of effective contraception, one of which has to be a barrier method (e.g., condom with spermicidal foam/gel/film/cream) for the duration of the trial and for 12 weeks following the last dose of trial medication
boolean
ID.4
Item
participation in another trial within 90 days prior to screening
boolean
ID.5
Item
subjects with a history of or presence of cancer, diabetes, or any clinically significant cardiovascular, respiratory, metabolic, renal, hepatic, gastrointestinal (including gastroesophageal reflux disease and irritable bowel syndrome), endocrinological, haematological, dermatological, venereal, neurological, or psychiatric disease or other major disorders that might have an impact on the current trial, as judged by the investigator
boolean
ID.6
Item
subjects who are known to have hepatitis or who are carriers of the hepatitis b surface antigen (hbsag) or hepatitis c antibodies, or have a positive result to the test for human immunodeficiency virus (hiv) antibodies
boolean
ID.7
Item
history of acute idiopathic or chronic pancreatitis
boolean

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

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