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Набира участници Фаза 1 NCT07388667

A Clinical Study of MK-4082 in Healthy Overweight Participants (MK-4082-002)

Фаза 1 – тестване на безопасността при малка група хора
Заболявания: Healthy

Спонсор: Merck Sharp & Dohme LLC

Налично на: БГ
Обобщение
Researchers are looking for new weight loss medicines for people with higher body weight. The study medicine, MK-4082, is different from similar weight loss medicines because people take it as a pill instead of an injection. Before giving a study medicine to people with a health condition, researchers first do studies to find a safe dose level (amount) of the study medicine that can be used in future studies. The goals of this study are to learn about: * The safety of MK-4082 and if people tolerate it * What happens to different MK-4082 dose levels in a person's body over time
Кой може да участва
Inclusion Criteria: The main inclusion criteria include but are not limited to the following: * Is in good health * Has body mass index (BMI) between 25 and 40 kg/m\^2, inclusive. Participants must weigh at least 60 kg Exclusion Criteria: The main exclusion criteria include but are not limited to the following: * has a history of previous surgical treatment for obesity (bariatric surgery, gastric banding, etc.) or any other gastrointestinal (GI) surgery that may induce malabsorption, history of bowel resection \>20 cm, any malabsorption disorder, severe gastroparesis, or any GI procedure for weight loss (including LAP-BAND®), as well as clinically significant GI disorders (eg, peptic ulcers, severe gastroesophageal reflux disease) * has an individual or family history of medullary thyroid carcinoma or multiple endocrine neoplasia 2
Интервенции
MK-4082
DRUG
Placebo
DRUG
Места на провеждане 5
САЩ (5)
Anaheim Clinical Trials ( Site 0005)
Anaheim , California
Study Coordinator
ProSciento Inc. ( Site 0002)
Chula Vista , California
Study Coordinator
Hassman Research Institute Marlton Site ( Site 0006)
Marlton , New Jersey
Study Coordinator
QPS-MRA, LLC ( Site 0003)
South Miami , Florida
Study Coordinator
Bio-Kinetic Clinical Applications, LLD dba QPS-MO ( Site 0004)
Springfield , Missouri
ACTIVE_NOT_RECRUITING
Технически детайли
Статус
Набира участници
Фаза
Фаза 1
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
60 Years
Здрави доброволци
Не
Начална дата
04.03.2026
Крайна дата
19.08.2026
Регистрационен номер
NCT07388667
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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