Study on How Cagrilintide and Semaglutide Help People with Overweight or Obesity Reduce Weight

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What is this study about?

This clinical trial is focused on studying the effects of a new treatment called CagriSema for individuals who are experiencing overweight or obesity. The treatment involves a combination of two medications, cagrilintide and semaglutide, which are administered through a pen-injector device. The purpose of the study is to determine how well CagriSema helps in reducing body weight compared to a placebo, alongside a reduced-calorie diet and increased physical activity.

Participants in the study will receive a once-weekly injection of CagriSema or a placebo. The study will monitor changes in body weight, aiming for a reduction of at least 5% and potentially up to 30%. Other aspects being observed include changes in waist circumference, blood pressure, and quality of life related to weight. The study will also track any adverse events that may occur during the treatment period.

The trial is expected to continue until October 2026, with recruitment starting in November 2023. This research aims to provide valuable insights into the effectiveness and safety of CagriSema as a treatment option for managing overweight and obesity.

1 joining the study

Upon joining the study, participants will be informed about the purpose and procedures of the trial. The study aims to evaluate the effectiveness and safety of a combination of medications called CagriSema for weight loss in individuals with excess body weight.

Participants will be required to sign an informed consent form, confirming their understanding and willingness to participate in the study.

2 initial assessment

Participants will undergo an initial assessment to confirm eligibility. This includes checking age, body mass index (BMI), and any obesity-related health conditions.

Eligibility criteria include being 18 years or older, having a BMI of 30 or higher, or a BMI of 27 or higher with at least one obesity-related complication such as high blood pressure or sleep apnea.

3 medication administration

Participants will receive the study medication, CagriSema, which is a combination of two drugs administered via a subcutaneous injection (under the skin) once a week.

The medication is intended to be used alongside a reduced-calorie diet and increased physical activity to aid in weight loss.

4 ongoing monitoring

Throughout the study, participants will be regularly monitored to assess the effects of the medication on body weight and overall health.

Regular check-ups will include measurements of body weight, waist circumference, and blood pressure, as well as assessments of quality of life and physical functioning.

5 completion of the study

The study is expected to conclude by October 19, 2026. Participants will have a final assessment to evaluate the overall impact of the treatment.

The primary goal is to observe a reduction in body weight, with secondary goals including improvements in waist circumference, blood pressure, and quality of life.

Who Can Join the Study?

  • Must be male or female.
  • Must be 18 years or older at the time of signing the consent form.
  • Must have a Body Mass Index (BMI) of 30.0 kg/m2 or higher. BMI is a measure of body fat based on height and weight.
  • If BMI is between 27.0 and 29.9 kg/m2, must have at least one obesity-related health issue, such as:
    • Hypertension (high blood pressure)
    • Dyslipidaemia (abnormal amount of fats in the blood)
    • Obstructive sleep apnoea (a sleep disorder where breathing repeatedly stops and starts)
    • Cardiovascular disease (heart and blood vessel conditions)

Who Cannot Join the Study?

  • Participants cannot join if they have a history of any serious heart problems.
  • Individuals with uncontrolled high blood pressure cannot participate.
  • People with a history of cancer in the last 5 years are excluded, except for some skin cancers.
  • Participants with any major psychiatric disorders, which are mental health conditions affecting mood, thinking, and behavior, are not allowed.
  • Those who have had surgery for weight loss in the past are not eligible.
  • Individuals with a history of drug or alcohol abuse in the last year cannot take part.
  • Pregnant or breastfeeding women are not allowed to participate.
  • Participants who are currently involved in another clinical trial are excluded.
  • People with any other medical condition that the study doctors think would make it unsafe for them to participate are not eligible.

Where you can join this trial?

Verified and Recommended Sites

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Verified Sites

Other Sites

Site Name City Country Status
Turku University Hospital Turku Finland
Centre Hospitalier Universitaire De Nantes Nantes France
Diagnostic Consultation Center XX-Sofia EOOD Sofia Bulgaria
Hospital General Universitario Gregorio Maranon Madrid Spain
Hopital Beaujon Clichy France
Uniteversity Muliprofile Hospital For Active Treatment Tsaritsa Yoanna-Isul EAD Sofia Bulgaria
CHU Helora La Louviere Belgium
Instytut Diabetologii Sp. z o.o. Warsaw Poland
Chiaoigqg Uhrtcatfiyqajf Spnqisipi Woluwe-Saint-Lambert Belgium
Aniewey Obvstnsgjid di Pvgtcl Padua Italy
Mxvvfcrwyqfbx Bmkgptdf Zd Amgbosu Lvrhopby Pjib Ac Blagoevgrad Bulgaria
Drlfwzzpaqbrnrmbfvhbudh cfggsl “fgnjzatlumbhbzs Elfh Sofia Bulgaria
Rotkpt Sulxsigya Holbæk Denmark
Hgoyaoiu Czrbgr Dc Beitnztda Barcelona Spain
Hjssgxkv Uczdihswtv Crskcmq Hxlekwrq Helsinki Finland
Ugjoikcdfrcu Lhcnkmw Leipzig Germany
Ajpqezj Unnxm Shtguhfhx Ldielr Df Bnavkha Bologna Italy
Unzpyjjjfwehrp Cefdbdf Khghzirbd Gdansk Poland
Uglwrdsvjq Ob Abappom Edegem Belgium
Uoywuqigem Dkzmy Sgrmv Do Rcnc Ll Svjchlhw Rome Italy
Ukkmiincyelc Zowdfoqhvn Gtls Gent Belgium
Ctrprf Hnwhsqdlprb Lyzp Skm Pierre Benite France
Ohtn Uluobsaxob Hotjxflt Oulu Finland
Hqotrqgd Upvgpzplkqaklr Sazssxfylq &laipns Hxjyxcj di Hhpvynwvevi STRASBOURG, Alsace France
Uaawfjpysurmz Syvjgxa Krqphumyp W Biyjpafyfuq Bialystok Poland
Mlhcgdj Cvvkjx Bpxwpqbm Lcry Yambol Bulgaria
Smxcwikembw Pavgxrwzi Sdnrddm Kalvyqggb Itd Pwhci Wk Ormgswjqrkr Ciqp Warsaw Poland
Gkqkpvk Lfgjuurf Otefbgkq i Cjdmcw Dfdhbhaugelwlc Bialystok Poland
Ngdg Vzzr Djxblbtwp Mplgiyqdxu Bquokfjk Bialystok Poland
Mqjklsi Cdtcmp Abazj Irf Pzxartq Ehgh Sofia Bulgaria
Ohwoegjzja Cvjqny Fzo Ireccktani Pugenvgu Fmn Sydhiyfggrx Obgdvvipgd Mizviqx Clvw Ehxcwuaqfausn Nk Eiff Montana Bulgaria
Orhphftxwi Cppdhl fwl Sdqxsvdusww Oqjxyqbvhw Miljihi Cuby id Ecbdvcewqjmzy ann Mjkxpjgoa Dhgknbcj Ruse Bulgaria
Clgnxmh Khypcukoolineyvtth Gxhxykrjvrp Mwvtzp Ghxvnyp Bydgoszcz Poland
Cxkkahq Glrrkhefgtd Paqpeansciu I Lrsfsouc Nmcvpagkhzub Pltbglapt Sk zonnfb Poznan Poland
Iiedkijb fvqk Dgeiyfpiyuccpnauu Mcjfesda Gbha Munster Germany
Ascrkffkuv Fuj Isbedhomhk Paknbrmn Fjp Sqigydkiwmh Mqrwfzs Chsm Kcjscc Eoxe Varna Bulgaria
Iwsnq Pearcicafwb Slg Dfscoy San Donato Milanese Italy
Uvhuqnyrkltxotlnj Caocpp Byijsrufgu Dd Rivp Rome Italy
Abbovjs Oaryindthyx Ugiupmbsbsobj Stcrtt Siena Italy
Agffvz Ucxspdpjlp Hfjrpcmb Aarhus Denmark
Axsutzjyl Ujo Amsterdam The Netherlands
Bzyrim Zjsfklaqcv Roosendaal The Netherlands
Ztbquui fwkl kccqsnkhs Svfdozc Smsreulldbuconf Gyaf Elsterwerda Germany
Sfoztv Ljkwxjf I Mjiyw Sgt Jh Katowice Poland
Goglcvkp Hihjsift Hellerup Denmark
Rdzbfcxmf Zbrcnrxclq Spavvrwon Arnhem The Netherlands
Htqcwvoh Hqnbnkqs Hvidovre Denmark
Ucacqtlujp Mtrme Gnaxyvo Od Cocmuothp Catanzaro Italy
Ajyjz Gmaoxxlbs Dh Camvcha Catania Italy
Ifyaaw Bonheiden Belgium
Icwxmdtv Fksoylhwc Gpro Essen Germany
Cfjtvhe Movaphih Phqarew Mjwwdgrog Cwscbemn Loqkqisohn Mvmkoj Zdvnpybul soyzt Cracow Poland
Anjsla Smaepehjwo Zyulaidktp Dordrecht The Netherlands
Cuogcg Dg Rqachzhrc Cfuflrhm Ptwpqi Do Swd Venissieux France
Aiqpxft Gcxc Dmm Avbqvjxto Bcgetfhkhubhjvu Leipzig Germany
Bqabu Mtbpypnxjgof &pfks Dcnrkxn Dvruhwvxg Cmcysmzky Sdy jj Legnica Poland
Sgubiei Gvnrwepg Hoofddorp The Netherlands
Twfvi Syb z owyv sgspq Lublin Poland
Ajjbpinsb Mvkftnk Cjqvje Oxk Dupnitsa Bulgaria
Zftoyur fun kbnfgcqma Fcrmlxykm Aidduo Oajduouopikc Wangen Germany
Cjmvrwu Ztfivgf Mwgooqtpceespw Poznan Poland
Wlxtmvdkpkrzc Hzmnllh Hamburg Germany
Hgaqoytpi Dhqjk Eevsuwex &wcst Kcvmniwm Stuttgart Germany

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Not recruiting
03.11.2023
Bulgaria Bulgaria
Not recruiting
03.11.2023
Denmark Denmark
Not recruiting
03.11.2023
Finland Finland
Not recruiting
03.11.2023
France France
Not recruiting
03.11.2023
Germany Germany
Not recruiting
03.11.2023
Italy Italy
Not recruiting
03.11.2023
Poland Poland
Not recruiting
03.11.2023
Spain Spain
Not recruiting
03.11.2023
The Netherlands The Netherlands
Not recruiting
03.11.2023

Trial locations

Cagrilintide is a medication that is being tested to help people lose weight. It is given as an injection under the skin. This medication works by making you feel full, so you eat less. It is being studied to see if it can help people who are overweight or have obesity to reduce their body weight when combined with a healthy diet and exercise.

Semaglutide is another medication used in this study, also given as an injection under the skin. It helps control appetite and can lead to weight loss. Like cagrilintide, it is being tested to see if it can help people with overweight or obesity lose weight when used together with a reduced-calorie diet and increased physical activity.

Overweight and obesity – Overweight and obesity are conditions characterized by excessive body fat accumulation that may impair health. They develop when the energy intake from food and drink exceeds the energy expended through physical activity and metabolic processes. Over time, this energy imbalance leads to an increase in body weight and body fat. The progression of these conditions can result in increased body mass index (BMI), which is a measure of body fat based on height and weight. As body weight increases, individuals may experience changes in body shape and size, including increased waist circumference. These conditions can also affect physical function and quality of life, as they may lead to reduced mobility and increased strain on the body’s systems.

Trial ID:
2023-506929-11-00
Protocol code:
NN9838-4608
Trial Phase:
Therapeutic confirmatory (Phase III)

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