Phase 1 Obesity Trial, Recruiting NCT07331389 Sponsor: Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd. Condition: Obesity
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Phase 1 Obesity Trial, Recruiting

NCT07331389
Recruiting Phase 1

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 are considered to be in good general health based on their medical history, blood tests, vital signs, heart tracing (ECG), and physical examination during the screening period
  • People between the ages of 18 and 45 (inclusive), of any gender
  • People who weigh at least 50 kg and have a Body Mass Index (BMI) between 24.0 and 35.0 (a measure of body weight relative to height, inclusive of those values)

Who may not be able to join:

  • People with a personal or family history of a type of thyroid cancer called medullary thyroid cancer, abnormal thyroid cell growth (C-cell hyperplasia), or a hormonal condition called Multiple Endocrine Neoplasia type 2 (MEN2), or whose calcitonin (a hormone measured in blood) is at or above a certain level at screening
  • People with a history of long-term (chronic) inflammation of the pancreas, or who have had an acute pancreas attack within the 3 months before screening
  • People who have had an acute gallbladder attack within the 3 months before screening
  • People who have had a severe low blood sugar episode, or repeated low blood sugar episodes, within the 3 months before screening
  • People who have difficulty swallowing, or conditions affecting how the stomach empties or absorbs nutrients — such as previous weight-loss surgery, stomach removal surgery, irritable bowel syndrome, or persistent indigestion (confirm with trial site)
  • People with pre-existing conditions that increase the risk of bleeding, such as stomach ulcers with active bleeding, or certain types of bleeding in or around the brain
  • People who have had previous surgery that may affect how the body processes medications, or who plan to have surgery during the study period
  • People whose physical examination, heart tracing (ECG), blood tests, or vital signs show any results considered medically significant during the screening period
  • People who have taken, or plan to take, any medication known to affect certain liver enzymes or drug-processing proteins within 28 days before starting the trial medication
  • People with a significant history of heart or stroke-related disease within the 6 months before screening, or at the time of admission to the trial
  • People whose heart tracing (ECG) shows results considered clinically significant by the investigating doctor at screening

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 22 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

GP referral letter

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

Trial details

Status
Recruiting
Phase
Phase 1
Sponsor
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
24 September 2025
Est. completion
12 January 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

AUC[0-∞]; Cmax; AUC[0-t]

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: 22 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