Phase 4 Type 2 Diabetes Trial, Recruiting NCT07244003 Sponsor: Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd. Condition: Type 2 Diabetes
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Phase 4 Type 2 Diabetes Trial, Recruiting

NCT07244003
Recruiting Phase 4

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with type 2 diabetes according to Chinese clinical guidelines (2020 edition)
  • People aged 18 to 75 years old (inclusive), of any gender
  • People with a Body Mass Index (BMI) of 20 or above — BMI is a measure calculated from height and weight
  • People who have been taking metformin (at a dose of 1000mg or more per day), with or without one other diabetes tablet (but not an SGLT-2 inhibitor or an oral GLP-1 medication), for at least 8 weeks before the screening visit, and whose blood sugar remains poorly controlled — specifically, a blood sugar marker called HbA1c must be between 7.5% and 11.0% as measured by the central lab
  • People who are willing to take part in the study and have signed a consent form

Who may not be able to join:

  • People who have type 1 diabetes, or any other specific type of diabetes other than type 2
  • People who experienced a serious diabetes-related emergency (such as diabetic ketoacidosis, hyperosmolar state, or lactic acidosis) within the 6 months before screening
  • People who have used a GLP-1 or SGLT-2 type diabetes medication within the 12 weeks before screening, or who have previously tried and stopped one of these medications because it did not work well enough
  • People who received insulin treatment in the week before screening
  • People who have a history of pancreatitis (inflammation of the pancreas), whether past or current, or who have very high triglyceride (blood fat) levels at screening (above 5.7 mmol/L)
  • People whose liver is not functioning well at screening — specifically, if certain liver test results (ALT, AST, or total bilirubin) are significantly above the normal range
  • People whose kidneys are not functioning well enough at screening — assessed using a standard kidney function calculation (eGFR at or below 45 mL/min/1.73m²) or elevated creatinine levels
  • People who have a personal or family history of a specific type of thyroid cancer (medullary thyroid cancer), or a condition called Multiple Endocrine Neoplasia type 2 (MEN2)
  • People who are currently pregnant, breastfeeding, or planning to become pregnant during the study period
  • People who have had an allergic reaction or known sensitivity to metformin, dapagliflozin, liraglutide, or any ingredients in these study medications
  • People who have taken part in another clinical drug trial within the 3 months before screening
  • People who, in the opinion of the trial doctor, are unable to follow the study plan, or who have other serious physical or mental health conditions that could affect the study results or their safety (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Phone: +86-0571-89908582

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 4
Sponsor
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
29 March 2025
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The change of HbA1c compared to the baseline

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov