Phase 1 Obesity Trial, Recruiting NCT07443059 Sponsor: Beijing QL Biopharmaceutical Co.,Ltd Condition: Obesity
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Phase 1 Obesity Trial, Recruiting

NCT07443059
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.
  • People aged between 18 and 75 years old at the time of signing the consent form.
  • People with a body mass index (BMI) between 19.0 and 32.0, and who weigh at least 50 kg (for men) or at least 45 kg (for women).
  • People who have been diagnosed with stable, long-term kidney disease for at least 3 months.
  • People whose kidney function — measured by a specific kidney filtration test (eGFR) — falls into one of four categories: normal kidney function, mild reduction in kidney function, moderate reduction in kidney function, or severe reduction in kidney function.
  • People whose kidney function has remained stable across two separate measurements taken during the screening period.

Who may not be able to join:

  • People with a history of pancreas inflammation (pancreatitis) or pancreatic injury.
  • People with a personal or family history of a specific type of thyroid cancer (medullary thyroid carcinoma) or a related hormonal condition (type 2 multiple endocrine neoplasia).
  • People with a history of depression, anxiety disorder, or any severe psychiatric condition.
  • People who have had any type of cancer in the 5 years before screening, whether treated or not (with the exception of a certain type of skin cancer called basal cell carcinoma, or cervical carcinoma in situ that has been cured).
  • People in the kidney disease group whose kidney problems are caused by blockages in the urinary tract, kidney tumours, narrowed kidney arteries, certain medications, severe infections, low blood volume, or heart failure — if the trial doctor considers this makes them unsuitable.
  • People in the kidney disease group whose blood pressure during screening is higher than 160/100 mmHg.
  • People in the kidney disease group who have taken certain medications that affect how the kidneys process a waste product called creatinine, or medications that are harmful to the kidneys, within 14 days before screening (or longer, depending on the medication).
  • People in the normal kidney function group who have had significant health conditions affecting the heart, lungs, digestive system, hormones, blood, or mental health within the past year, if the trial doctor considers this makes them unsuitable.
  • People in the normal kidney function group whose blood pressure falls outside the range of 90–140 mmHg (systolic) or 50–90 mmHg (diastolic).
  • People in the normal kidney function group who have taken any medications — including prescription drugs, over-the-counter medicines, herbal medicines, or supplements such as vitamins and minerals — within 14 days before screening (or longer, depending on the medication).

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 27 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

Principal Investigator: Wei Zhao, PhD, The First Affiliated of Shandong First Medical University

Phone: +86-010-61702599

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
Beijing QL Biopharmaceutical Co.,Ltd
Registry
ClinicalTrials.gov
Start date
13 April 2026
Est. completion
3 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Area Under the Concentration Versus Time Curve (AUC) of ZT002 From Time Zero to Tlast (AUC0-t).; Maximum Concentration of ZT002 (Cmax); Area Under the Concentration Versus Time Curve (AUC) of ZT002 From Time Zero to Infinity (AUC0-∞); Time to maximum concentration (Tmax); Apparent terminal half-life (t1/2); Apparent clearance (CL/F); Incidence and severity of adverse events

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: 27 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