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A Phase III, Randomised, Double-blind, Placebo-controlled, Multicentre Study to Evaluate the Efficacy and Safety of Elecoglipron in Asian Participants With Obesity or Overweight With or Without Type 2 Diabetes Mellitus (EMBOLD-Asia)

Status: Recruiting
Location: See all (49) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

The purpose of this study is to evaluate the efficacy and safety of elecoglipron compared with placebo adjunct to diet and exercise for weight management, in adult participants living with obesity or overweight with or without T2DM.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adult participant aged 18 years or older at the time of informed consent.

• Body mass index (BMI) at screening of:

• 28 kg/m\^2 or higher, or

• 24 kg/m\^2 to less than 28 kg/m\^2 with at least 1 weight-related comorbidity.

• Stable body weight (self-reported or documented) for 90 days prior to the screening visit (± 5% body weight change)

• History of at least 1 self-reported unsuccessful dietary effort to lose body weight.

• Participants with type 2 diabetes mellitus, if enrolled, and have HbA1c from 6.5% to less than 10.0% at screening.

Locations
Other Locations
China
Research Site
NOT_YET_RECRUITING
Baotou
Research Site
NOT_YET_RECRUITING
Beijing
Research Site
NOT_YET_RECRUITING
Beijing
Research Site
NOT_YET_RECRUITING
Beijing
Research Site
NOT_YET_RECRUITING
Changde
Research Site
NOT_YET_RECRUITING
Changsha
Research Site
NOT_YET_RECRUITING
Changzhou
Research Site
RECRUITING
Chengdu
Research Site
NOT_YET_RECRUITING
Hefei
Research Site
NOT_YET_RECRUITING
Huangshi
Research Site
RECRUITING
Jincheng
Research Site
NOT_YET_RECRUITING
Jinzhou Shi
Research Site
NOT_YET_RECRUITING
Langfang
Research Site
NOT_YET_RECRUITING
Luoyang
Research Site
NOT_YET_RECRUITING
Meihekou
Research Site
NOT_YET_RECRUITING
Nanjing
Research Site
NOT_YET_RECRUITING
Nanyang
Research Site
NOT_YET_RECRUITING
Nanyang
Research Site
NOT_YET_RECRUITING
Shanghai
Research Site
NOT_YET_RECRUITING
Shantou
Research Site
NOT_YET_RECRUITING
Shenyang
Research Site
NOT_YET_RECRUITING
Shenyang
Research Site
NOT_YET_RECRUITING
Shijiazhuang
Research Site
WITHDRAWN
Wuhan
Research Site
NOT_YET_RECRUITING
Wuhu
Research Site
NOT_YET_RECRUITING
Xianyang
Research Site
NOT_YET_RECRUITING
Xuzhou
Research Site
NOT_YET_RECRUITING
Yan’an
Research Site
NOT_YET_RECRUITING
Yueyang
Research Site
NOT_YET_RECRUITING
Zhumadian
Research Site
NOT_YET_RECRUITING
Zibo
Hong Kong Special Administrative Region
Research Site
RECRUITING
Hong Kong
Research Site
NOT_YET_RECRUITING
Randwick
Malaysia
Research Site
NOT_YET_RECRUITING
Alor Star
Research Site
NOT_YET_RECRUITING
Kuala Lumpur
Research Site
NOT_YET_RECRUITING
Kuching
Research Site
NOT_YET_RECRUITING
Putrajaya
Research Site
NOT_YET_RECRUITING
Sarawak Miri
Research Site
NOT_YET_RECRUITING
Seremban
Research Site
NOT_YET_RECRUITING
Seri Manjung
Research Site
NOT_YET_RECRUITING
Sungai Buloh
Philippines
Research Site
NOT_YET_RECRUITING
Davao City
Research Site
NOT_YET_RECRUITING
Iloilo City
Research Site
NOT_YET_RECRUITING
Manila
Thailand
Research Site
NOT_YET_RECRUITING
Bangkok
Research Site
NOT_YET_RECRUITING
Bangkok
Research Site
NOT_YET_RECRUITING
Chiang Mai
Research Site
NOT_YET_RECRUITING
Phutthamonthon
Research Site
NOT_YET_RECRUITING
Songkhla
Contact Information
Primary
AstraZeneca Clinical Study Information Center
information.center@astrazeneca.com
1-877-240-9479
Time Frame
Start Date: 2026-08-21
Estimated Completion Date: 2028-04-20
Participants
Target number of participants: 351
Treatments
Experimental: Arm 1 - Dose 1
Active IMP
Experimental: Arm 2 - Dose 2
Active IMP
Placebo_comparator: Arm 3 - Placebo
Placebo matching elecoglipron
Related Therapeutic Areas
Sponsors
Leads: AstraZeneca

This content was sourced from clinicaltrials.gov