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Taking people in Egyesült Arab Emírségek3. fázis

A Study of Orforglipron (LY3502970) in Participants With Type 2 Diabetes Who Observe Ramadan Fasting

Key facts

Where
Abu Dhabi, Al Ain City és Dubai, Egyesült Arab EmírségekSee the 7 sites
Phase
3. fázis

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Forrás: NCT07613307: ki vehet részt

Where in Egyesült Arab Emírségek

  • Burjeel Medical CityAbu Dhabi, Egyesült Arab EmírségekToborzás még nem indult
  • NMC Abu DhabiAbu Dhabi, Egyesült Arab EmírségekTaking people
  • NMC Royal hospitalAbu Dhabi, Egyesült Arab EmírségekTaking people
  • Sheikh Khalifa Medical CityAbu Dhabi, Egyesült Arab EmírségekTaking people
  • Tawam HospitalAl Ain City, Egyesült Arab EmírségekTaking people
  • Dubai HospitalDubai, Egyesült Arab EmírségekTaking people
  • Emirates Hospital DubaiDubai, Egyesült Arab EmírségekToborzás még nem indult

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Eli Lilly and Company
Trial code
NCT07613307
Record updated
2026. október 8.
Original description
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.Read full original descriptionShow less

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)

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.

Inclusion: 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.

Exclusion: Have a history of chronic or acute pancreatitis any time prior to screening; 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 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; Have evidence of a significant, uncontrolled endocrine abnormality, for example, thyrotoxic or adrenal crises, in the opinion of the investigator.

ClinicalTrials.gov NCT07613307