A Study of Orforglipron (LY3502970) in Participants With Type 2 Diabetes Who Observe Ramadan Fasting
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Orforglipron.
- Кому может быть актуально
- Состояния в реестре: Diabetes Mellitus, Type 2, Diabetes Melletus, Glucose Metabolism Disorders, Metabolic Disorders. Базовые параметры: 18 лет — 65 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Индия, Саудовская Аравия, ЮАР, ОАЭ
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
A Phase 3b, Multicenter, Multi-Country, Open-Label, Single-Arm Study to Investigate the Efficacy and Safety of Orforglipron in Adult Participants With Type 2 Diabetes Who Observe Ramadan Fasting (ACHIEVE-RAM)
Обзор
The purpose of this study is to test the efficacy and safety of orforglipron in participants with T2D (type 2 diabetes) who participate in fasting during Ramadan. For each participant, the study will last up to 48 weeks with a minimum of 7 in clinic visits and 4 virtual visits.
Вмешательства
- Препарат Orforglipron
Administered orally
Первичные конечные точки
- Change from Baseline in Hemoglobin A1C (HbA1c) [Срок оценки: Baseline, up to 8 Weeks after Start of Ramadan]
Вторичные конечные точки (6)
- Percentage of Participants with an HbA1c of less than (<) 7 Percent (%) (53 millimeters per mole (mmol/mol)) [Срок оценки: Baseline, Up to 8 Weeks after Start of Ramadan]
- Change From Baseline in Fasting Serum Glucose (FSG) [Срок оценки: Baseline, Up to 8 Weeks after Start of Ramadan]
- Percent Change from Baseline in Body Weight [Срок оценки: Baseline, Up to 8 Weeks after Start of Ramadan]
- Change in EuroQol 5-Dimension 5-Level (EQ-5D-5L) Index [Срок оценки: Baseline, Up to 8 Weeks after Start of Ramadan]
- Percent Change in HbA1c [Срок оценки: 4 Weeks Prior to Ramadan, Up to Week 8 after Start of Ramadan]]
- Percent Change in Body Weight [Срок оценки: 4 Weeks Prior to Ramadan, Up to Week 8 after Start of Ramadan]]
Критерии участия
Критерии включения
- Have a clinical diagnosis of T2D based on the World Health Organization (WHO) classification or other locally applicable diagnostic standards.
- Have an HbA1c value of at least 7.0% (53 millimoles per mole (mmol/mol)) to less than 9.5% (91 mmol/mol) at screening.
- Intend to be compliant with the fast during the Ramadan period.
- Have had stable body weight self-reported change of 5 kilograms (kg) or lower during the 90 days prior to screening.
- Have body mass index (BMI) of 25 kilograms per meter square (kg/m2) or higher at screening.
Критерии исключения
- Have any form of diabetes other than T2D, including type 1 diabetes (T1D), gestational diabetes, latent autoimmune diabetes, maturity-onset diabetes of the young, and medication-induced diabetes
- Have a family (first-degree relative) or personal history of medullary thyroid carcinoma or multiple endocrine neoplasia syndrome type 2.
- Have a history of chronic or acute pancreatitis any time prior to screening
- Have evidence of a significant, uncontrolled endocrine abnormality, for example, thyrotoxic or adrenal crises, in the opinion of the investigator
- Have a history of an active or untreated malignancy or are in remission from a clinically significant malignancy for less than 5 years.
- Have a history of cholecystectomy (surgically removed gallbladder)
- Have New York Heart Association Functional Classification IV congestive heart-failure.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Не применимо
- Модель
- Одна группа
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
ЮАР · 14 центров
- JOSHA Research — Bloemfontein
- TREAD Research — Cape Town
- TASK Central — Cape Town
- Tiervlei Trial Centre — Cape Town
- Synopsis Research — Cape Town
- Synergy Biomed Research Institute (SBRI) — East London
- Aliwal Shoal Medical Centre — eMkhomazi
- Fola Health — Johannesburg
- … и ещё 6 центров
Индия · 9 центров
- Sarojini Naidu Medical College — Agra
- Osmania General Hospital — Hyderabad
- Brij Medical Centre Pvt. Ltd. — Kanpur
- Apollo Multispeciality Hospitals limited — Kolkata
- KGN Diabetes and Endocrinology Centre — Mumbai
- Mysore Medical College and Research Institute — Mysore
- Supe Heart & Diabetes Hospital & Research Centre — Nashik
- Diabetes Clinic — Nellore
- … и ещё 1 центр
Саудовская Аравия · 9 центров
- King Abdulaziz University for Health Sciences Ministry of National Guard Health Affairs — Al-Ahsa
- King Fahad Specialist Hospital — Dammam
- National Guard Health Affairs: King Abdulaziz Medical City — Jeddah
- Dr. Soliman Fakeeh Hospital — Jeddah
- King Abdulaziz University Hospital — Jeddah
- King Fahad Armed Forces Hospital Jeddah — Jeddah
- King Saud University Medical City — Riyadh
- Dr. Soliman Fakeeh Hospital — Riyadh
- … и ещё 1 центр
ОАЭ · 5 центров
- Sheikh Khalifa Medical City — Abu Dhabi
- NMC Abu Dhabi — Abu Dhabi
- Tawam Hospital — Al Ain City
- Emirates Hospital Dubai — Dubai
- Dubai Hospital — Dubai
Идентификаторы
NCT: NCT07613307 · 27746 · J2A-MC-GZPV