Study on the Effectiveness and Safety of Oral Semaglutide Compared to Placebo in Children and Adolescents with Type 2 Diabetes Using Metformin or Basal Insulin

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What is this study about?

This clinical trial is focused on studying Type 2 diabetes in children and teenagers. The study is testing a new medicine called oral semaglutide, which is taken in the form of tablets. The trial will compare the effects of oral semaglutide with a placebo, which is a tablet that looks like the medicine but does not contain the active ingredient. The purpose of the study is to see if oral semaglutide can help control blood sugar levels better than the placebo in young people who are already taking other diabetes medications like metformin or basal insulin.

Participants in the study will take either oral semaglutide or the placebo for a period of up to 52 weeks. The study will monitor changes in blood sugar levels, body weight, and other health indicators over this time. The goal is to determine if oral semaglutide is safe and effective for managing Type 2 diabetes in children and adolescents. The study will also look at how the body processes the medicine and any potential side effects that may occur during the trial.

Throughout the study, participants will have regular check-ups to track their progress and ensure their safety. The trial aims to provide valuable information on the use of oral semaglutide in young people with Type 2 diabetes, potentially offering a new treatment option for managing this condition. The results of this study could help improve the care and treatment of children and teenagers living with diabetes.

1 joining the study

Upon joining the study, informed consent from a parent or legal representative is required, along with the child’s assent.

Eligibility is confirmed based on age (10 to <18 years), a diagnosis of type 2 diabetes, and current treatment with metformin and/or basal insulin.

2 initial assessment

An initial assessment is conducted to establish baseline measurements, including glycosylated hemoglobin (HbA1c) levels, fasting plasma glucose, body mass index (BMI), and other health indicators.

3 medication administration

Participants receive either oral semaglutide or a placebo. The semaglutide is administered in tablet form, with doses of 3 mg, 7 mg, or 14 mg, depending on the maximum tolerated dose.

The medication is taken orally, and the dosage may be adjusted during the trial based on individual tolerance.

4 ongoing monitoring

Regular monitoring occurs throughout the trial to assess changes in HbA1c, fasting plasma glucose, BMI, body weight, and other health parameters.

Participants attend scheduled visits for pharmacokinetic sampling and other assessments to evaluate the effects of the medication.

5 midpoint evaluation

At week 26, a comprehensive evaluation is conducted to measure changes from baseline in various health indicators, including HbA1c and fasting plasma glucose.

The effectiveness of the treatment is assessed, and any necessary adjustments to the medication regimen are made.

6 final assessment

At week 52, a final assessment is performed to evaluate long-term changes in health indicators and the overall effectiveness of the treatment.

The study concludes with a review of all collected data to determine the impact of oral semaglutide compared to the placebo.

Who Can Join the Study?

  • Consent must be given by the parent(s) or a legally acceptable representative, and the child must agree to participate before any trial-related activities begin. These activities include any procedures done as part of the trial to check if the child can join.
  • The child must be a boy or girl aged between 10 and less than 18 years old on the day they are randomly assigned to a group in the trial.
  • The child’s blood sugar level, measured by a test called HbA1c, must be between 6.5% and 11.0%. This test shows the average blood sugar level over the past 2 to 3 months.
  • The child must have been diagnosed with type 2 diabetes according to the guidelines of the American Diabetes Association. They should be treated with a stable dose of metformin (a medication to control blood sugar), or a stable dose of metformin and a stable dose of basal insulin (a long-acting insulin), or just a stable dose of basal insulin.

Who Cannot Join the Study?

  • Patients who are not between the ages of 10 and 18 years old.
  • Patients who do not have Type 2 diabetes. This is a condition where the body does not use insulin properly, leading to high blood sugar levels.
  • Patients who are not already being treated with metformin or basal insulin, or both. Metformin is a medication that helps control blood sugar levels, and basal insulin is a type of insulin that works throughout the day to keep blood sugar stable.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Unidade Local De Saúde De Santa Maria, E.P.E. Lisbon Portugal

Other Sites

Site Name City Country Status
University Hospital Ostrava Ostrava Czechia
Hospital Da Luz S.A. Lisbon Portugal
Gxwniyb Ubwqwpbajw Hbgahgbu Og Lzaziht Larissa Greece
Uxcentorpg Gcdgffo Hduhtvro Ow Tgvvvrydiami Atpxm Thessaloniki Greece
Uzgqdckyti Gndaspp Hpgacaek Oq Iwebvprz Ioannina Greece
Aactss Msdosft Cfqmxk Scjh Thessaloniki Greece
Ulmeysomvjp Sojquhnv Salzburg Austria
Unkysglwlj Gparhnw Hnspnimi Amqtwwi Gskmrqo Htntorad Ov Wbwf Amflwp H Athx Vdzxkch Chaidari Greece
Ptauvyk Cfstsxnga Gdgorcf Hvlpxfww Penteli Greece
Scltxyoc Cpbmwr dt Ufoxcyk pcqqez Cathi &etbcmarewfitzpvqukdkrr Bucharest Romania
Stuytlkg Julkgoxm dq Uusnzpu Tvxwnswbhb Targoviste Romania
Dwyvxs Cnaeyy Saxpnf Brasov Romania
Spiaahoi Cshtgl Jezhdqvb Dm Ujgkzeg Sdarbgy Ahphtcf Abxngk Ckgwlvrur Constanta Romania
Jbzbff Bhcxx Zcrvkhlvhc Sbprvxder S-Hertogenbosch The Netherlands
Uzpfrmq Lruig Dq Sggcr Dp Glcgcqfwmdkh Ebbkzu Vila Nova De Gaia Portugal
Ezyibfgwhl Ghokeog Cipqrf Oe Tvdnkqhbetif Thessaloniki Greece
Kpksvkf zctlsplog adhl Teplice Czechia
Ghazfty Huwqgrhe Ov Lcmyf Lamia Greece
Hathi Ddvazc Hmttugpy Ciyyvf Athens Greece

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
02.11.2020
Czechia Czechia
Not recruiting
02.11.2020
Greece Greece
Not recruiting
02.11.2020
Portugal Portugal
Not recruiting
02.11.2020
Romania Romania
Not recruiting
02.11.2020
The Netherlands The Netherlands
Not recruiting
02.11.2020

Trial locations

Investigated Drugs:

Oral Semaglutide is a medication being tested to see if it can help control blood sugar levels in children and adolescents with type 2 diabetes. It is taken by mouth and is being compared to a placebo to see if it works better at managing diabetes when used alongside other treatments like metformin or basal insulin.

Metformin is a common medication used to help control blood sugar levels in people with type 2 diabetes. It works by decreasing the amount of sugar the liver makes and helps the body respond better to insulin.

Basal Insulin is a long-acting insulin used to help control blood sugar levels throughout the day and night. It is often used in combination with other diabetes medications to help maintain stable blood sugar levels.

Investigated Diseases:

Type 2 diabetes – This is a chronic condition that affects the way the body processes blood sugar (glucose). In type 2 diabetes, the body either resists the effects of insulin, a hormone that regulates the movement of sugar into cells, or doesn’t produce enough insulin to maintain normal glucose levels. Over time, high blood sugar levels can lead to various health issues, including nerve damage, kidney problems, and vision loss. The disease often develops slowly, and individuals may not notice symptoms initially. Common symptoms include increased thirst, frequent urination, hunger, fatigue, and blurred vision. Lifestyle factors such as obesity and inactivity are significant contributors to the development of type 2 diabetes.

Trial ID:
2023-506923-27-00
Protocol code:
NN9924-4437
Trial Phase:
Therapeutic confirmatory (Phase III)

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