Phase 1 Obesity Trial, Recruiting NCT07150962 Sponsor: Fujian Shengdi Pharmaceutical Co., Ltd. Condition: Obesity
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Phase 1 Obesity Trial, Recruiting

NCT07150962
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 able to understand the trial procedures and possible side effects, and are willing to sign a written consent form
  • Male participants aged 18 to 55 years old at the time of signing the consent form
  • People with a body weight of at least 65 kg and a body mass index (BMI) between 24.0 and 35.0 (a measure of body weight relative to height)
  • People whose weight has not changed by more than 5 kilograms in the past 3 months
  • People who have been assessed by the trial doctors — through medical history, physical checks, vital signs, blood tests, and a heart tracing (ECG) — and determined to be suitable overweight or obese participants

Who may not be able to join:

  • People who are known or suspected to be allergic to any ingredient in the trial drug or related products, or who have a history of multiple, severe, or serious allergic reactions to medicines or foods
  • People with a chronic or serious medical history affecting the lungs, heart, digestive system, kidneys, blood, hormones, immune system, nerves, or mental health, or who currently have any of these conditions and are judged by the trial doctors to be unsuitable
  • People with a history of high blood pressure, or whose blood pressure readings during screening are considered abnormal and clinically significant by the trial doctors
  • People with a notable history of digestive or stomach problems (such as nausea, vomiting, heartburn, or diarrhoea), conditions that slow stomach emptying, any prior stomach or bowel surgery (except removal of intestinal polyps or the appendix), or who had acute diarrhoea in the 7 days before joining
  • People who have taken part in a clinical trial of any medicine or medical device within the 3 months before dosing, or within 5 half-lives of that drug — whichever period is longer
  • People who have donated blood or lost 400 mL or more of blood in the 3 months before dosing, or 200 mL or more in the month before dosing, or who received a blood transfusion within the 3 months before dosing
  • People who test positive for Hepatitis B, Hepatitis C, HIV, or syphilis
  • People with a history of drug abuse or illicit drug use, or who test positive on a urine drug screening test during the screening period
  • People who drink heavily (averaging 14 or more units of alcohol per week in the 6 months before screening), smoke 5 or more cigarettes per day on average, are unable to stop smoking or drinking during the trial, or who test positive on a blood alcohol test (confirm with trial site for exact definitions)

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 26 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.

Contact this trial

Phone: +86-0518-82342973

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 1
Sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
15 October 2025
Est. completion
1 February 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Area under the curve from Time Zero to Time of last quantifiable concentration (AUCtau); Adverse event (AE); Serious adverse event (SAE)

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: 26 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