Diese Studie enthält eine ausreichend große Teilnehmerzahl. Sie können sich hierfür nicht mehr an- oder abmelden.

Diabetes Typ 1

Ort der Studie

  • Geschlecht Beides
  • Alter von 18 bis 65
  • Gewicht in kg von 50 bis 200
  • Rauchgewohnheiten Nicht
  • Nur für Frauen, die keine Kinder mehr gebären können
  • BMI von 18 bis 30
  • Berechnen Sie Ihren BMI hier

Diabetes Typ 1


Clinical trial of a new compound that is being developed for the treatment of type 1 diabetes and inflammatory bowel disease

 

The research physician about this research

This clinical trial will investigate a new drug that has been developed for the treatment of type 1 diabetes and inflammatory bowel diseases. It looks at how safe the compound is and how well it is tolerated when it is used by healthy participants.

Note: As a woman you can only participate in this study if you have been sterilized or if you have passed the menopause. 

Für Deutschland: Bitte beachten Sie: Die Arzneimittelstudien finden im niederländischen Groningen statt. Sie müssen Englisch oder Niederländisch sprechen, verstehen und lesen können, um an einer Studie teilnehmen zu können. 

Important information about this study

  • The medical screening will take place in Groningen or Utrecht
  • The study compound will be given once during this trial.
  • The short visits will take place between 10:00 and 12:00 AM

 

Group 5b 5 Tage Aufenthalt
14 Aug 2023 bis einschl. 18 Aug 2023
kurzer Besuch
19 Aug 2023
22 Aug 2023
25 Aug 2023
29 Aug 2023
5 Sep 2023
12 Sep 2023
19 Sep 2023
26 Sep 2023
10 Okt 2023
24 Okt 2023
7 Nov 2023
Nachuntersuchung
21 Nov 2023
€ 4.290
Group 5c 5 Tage Aufenthalt
17 Aug 2023 bis einschl. 21 Aug 2023
kurzer Besuch
22 Aug 2023
25 Aug 2023
28 Aug 2023
1 Sep 2023
8 Sep 2023
15 Sep 2023
22 Sep 2023
29 Sep 2023
13 Okt 2023
27 Okt 2023
10 Nov 2023
Nachuntersuchung
24 Nov 2023
€ 4.290

 

Who can participate?

  • You are a healthy male or female.
  • You are between 18 and 65 years old.
  • Your weight is minimal 50 kg and your Body Mass Index (BMI) is between 18.0 and 30.0 kg/m2. 
  • You do not smoke and do not use any nicotine-containing products from 3 months prior to the compound administration in the trial.

Note:

  • You cannot participate in the trial if you have participated in another clinical trial in the 30 days prior to the first compound administration in this clinical trial (counting from the follow-up visit).
  • For this trial, you cannot (have) receive(d) a COVID-19 vaccine within 7 days prior to the start until 14 days after compound administration (in the period after in consultation with the doctor).
  • To determine if you are suitable to participate in this trial, you will undergo a medical screening. Depending on availability, this can be performed in Groningen or in Utrecht.

As a female you can only participate if you are not pregnant, not breast feeding and meet one of the following conditions:

  • You have passed the menopause (no periods for at least 12 consecutive months);
  • You are physiologically incapable of becoming pregnant;
  • You have been sterilized.

As a male you can only participate if you meet one of the following conditions:

  • You are using a condom in combination with an additional contraception method used by your female partner;
  • You have been sterilized or your female partner is sterilized or has passed the menopause (no periods for at least 12 months);
  • You are not sexually active;
  • You are only sexually active with a partner of the same sex.

 

Compensation

  • You will receive a gross compensation of € 3900 for participation in one of the groups of this study.

Travelling expenses will be reimbursed based on the distance traveled (€ 0,21 net per kilometer) with a minimum of € 13,- and a maximum of € 176,40 (840 kilometers) per round trip, regardless of the mode of transportation.

 

Period of stay and research

The trial consists of 1 period during which you will stay in the research facility in Groningen (location van Swietenlaan 6) for 5 days (4 nights), followed by 12 short visits including the follow-up.

Note: You must be available for all dates to be able to participate in this clinical trial. 

 

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