Efficacy, Safety, and Tolerability of Once Daily Oral Administration of AZD5004 Versus Placebo for 26 Weeks in Adults With Type 2 Diabetes Mellitus.

Phase
Recruitment status
Participants
Lead sponsor
Start date
Number of sites

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
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
Registry reports results
Listing at source
Recruitment status
Phase
Study type
Interventional

Completion date
First posted
Registry last updated
Primary completion date
Start date

Actual participants
Participants
Participant count basis
Protocol amendments
Number of sites

Data monitoring committee
Registry sponsor category
Lead sponsor
Source registry
ClinicalTrials.gov

Registry ID
ClinicalTrials.gov ID
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
Sources for study design

  1. Change in HbA1c

    Timeframe: Baseline to Week 26

    To evaluate the effect of AZD5004 versus placebo on glycemic control

  1. Change in fasting glucose

    Timeframe: Baseline to Weeks 4, 12, 16 and 26

    To evaluate the effect of AZD5004 versus placebo on fasting glucose

  2. Achievement of HbA1c ≤ 6.5%

    Timeframe: Week 26

    To evaluate of the effect of AZD5004 versus placebo on HbA1c

  3. Baseline HbA1c ≥ 7.0% and achieved HbA1c < 7.0%

    Timeframe: Week 26

    To evaluate the effect of AZD5004 versus placebo on HbA1c

  4. Percent change in body weight

    Timeframe: Baseline to Week 26

    To evaluate the effect of AZD5004 versus placebo on weight loss

  5. Absolute change in body weight

    Timeframe: Baseline to Week 26

    To evaluate the effect of AZD5004 versus placebo on weight loss

  6. Achievement of ≥ 5%, ≥ 10%, and ≥ 15% weight reduction

    Timeframe: Baseline to Week 26

    To evaluate the effect of AZD5004 versus placebo on weight loss

Sources for outcomes

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.

Sources for eligibility

  • 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.

Sources for sites

Other registry identifiers

  • 2024-512562-34-00
Sources for references

Related records

Drugs (1)

Lead sponsors (1)

Conditions (1)

Targets (1)