Efficacy, Safety, and Tolerability of Once Daily Oral Administration of AZD5004 Versus Placebo for 26 Weeks in Adults With Type 2 Diabetes Mellitus.
- Summary
- This is a Phase IIb, randomised, double-blind, parallel-group, placebo-controlled study to evaluate the efficacy, safety and tolerability of AZD5004 in adults with type 2 diabetes mellitus, compared to placebo and active comparator.
- Acronym
- SOLSTICE
- Short title
- Efficacy, Safety, and Tolerability of Once Daily Oral Administration of AZD5004 Versus Placebo for 26 Weeks in Adults With Type 2 Diabetes Mellitus.
- Official title
- A Phase IIb, Randomized, Double-blind, Placebo-controlled and Open-label Active Comparator Study to Evaluate the Efficacy, Safety, and Tolerability of AZD5004 in Adults With Type 2 Diabetes Mellitus.
- Control arm
- Placebo
- Registry reports results
- Listing at source
- Listed
- Recruitment status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Completion date
- 2025-12-19
- First posted
- 2024-08-30
- Registry last updated
- 2026-01-13
- Primary completion date
- 2025-12-19
- Start date
- 2024-10-08
- Actual participants
- Participants
- Participant count basis
- Actual
- Protocol amendments
- Number of sites
- Data monitoring committee
- Registry sponsor category
- Industry
- Lead sponsor
- AstraZeneca
- Source registry
- ClinicalTrials.gov
- Registry ID
- NCT06579105
- ClinicalTrials.gov ID
- NCT06579105
- Registry record
- Open registry record
- Allocation
- Randomised
- Model
- Parallel groups
- Purpose
- Treatment
- Masking
- Triple masking
- Masking description
- Masking (blinding) applies to patients and investigators involved in AZD5004 and placebo arms, however not in active comparator arm.
- Masked roles
- Participants, Care providers, Investigators
Change in HbA1c
Timeframe: Baseline to Week 26
To evaluate the effect of AZD5004 versus placebo on glycemic control
Change in fasting glucose
Timeframe: Baseline to Weeks 4, 12, 16 and 26
To evaluate the effect of AZD5004 versus placebo on fasting glucose
Achievement of HbA1c ≤ 6.5%
Timeframe: Week 26
To evaluate of the effect of AZD5004 versus placebo on HbA1c
Baseline HbA1c ≥ 7.0% and achieved HbA1c < 7.0%
Timeframe: Week 26
To evaluate the effect of AZD5004 versus placebo on HbA1c
Percent change in body weight
Timeframe: Baseline to Week 26
To evaluate the effect of AZD5004 versus placebo on weight loss
Absolute change in body weight
Timeframe: Baseline to Week 26
To evaluate the effect of AZD5004 versus placebo on weight loss
Achievement of ≥ 5%, ≥ 10%, and ≥ 15% weight reduction
Timeframe: Baseline to Week 26
To evaluate the effect of AZD5004 versus placebo on weight loss
- Sex
- All
- Age groups
- Adults, Older adults
- Minimum age
- 18 Years
- Healthy volunteers
- No
Adults ≥ 18 years of age.
Diagnosed with T2DM for at least 6 months.
HbA1c ≥ 7.0% and ≤ 10.5% managed with diet and exercise alone or with a stable dose of metformin or an SGLT2 inhibitor for at least one month prior to screening.
Body mass index of ≥ 23 kg/m2.
Stable self-reported body weight for 3 months prior to randomization (+/- 5% body weight change).
Type 1 diabetes mellitus, secondary forms of diabetes or history of ketoacidosis or hyperosmolar coma.
History of proliferative diabetic retinopathy, diabetic maculopathy, or severe non-proliferative diabetic retinopathy that required immediate treatment.
Have had more than one episode of severe hypoglycemia within 6 months prior to screening, or has a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms.
Received medication for weight loss within the last 3 months prior to screening.
Clinically significant inflammatory bowel disease, gastroparesis, severe disease or surgery affecting the upper GI tract.
Previous or planned (within study period) bariatric surgery or fitting of a weight loss device (eg, gastric balloon or duodenal barrier).
History of acute or chronic pancreatitis.
- Research SiteMobile, United States
- Research SiteSheffield, United States
- Research SiteVestavia Hills, United States
- Research SiteTucson, United States
- Research SiteLittle Rock, United States
- Research SiteLong Beach, United States
- Research SiteLos Angeles, United States
- Research SiteNewport Beach, United States
- Research SiteSacramento, United States
- Research SiteWaterbury, United States
- Research SiteLake City, United States
- Research SiteLargo, United States
- Research SiteOcoee, United States
- Research SiteOrlando, United States
- Research SiteDecatur, United States
- Research SiteSavannah, United States
- Research SiteLombard, United States
- Research SitePotomac, United States
- Research SiteBoston, United States
- Research SiteRoslindale, United States
- Research SiteFarmington Hills, United States
- Research SiteGulfport, United States
- Research SiteKansas City, United States
- Research SiteOmaha, United States
- Research SiteLas Vegas, United States
And 72 more, listed on the interactive page.
- PubMed 42259343Related publication
Other registry identifiers
- 2024-512562-34-00
Related records
Drugs (1)
Lead sponsors (1)
Conditions (1)
- Type 2 diabetes mellitus Primary condition