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NCT06893016RecruitingPhase 3

Evaluation of RAY1225 in Adult Participants Who Have Obesity or Are Overweight

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 3 Study Evaluating the Safety, Tolerability, and Efficacy of RAY1225 in Participants Who Have Obesity or Are Overweight

Source: ClinicalTrials.gov · Last updated 17 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The primary objective of this study is to demonstrate that RAY1225 is superior to placebo for percent change in body weight.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
640 (estimated)
First submitted
18 Mar 2025
Start date
15 Jun 2025
Primary completion date
15 Jun 2026
Lead sponsor
Guangdong Raynovent Biotech Co., Ltd
Diseases
Obesity
NCT number
NCT06893016

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 640
  • From 15 Jun 2025 to the primary completion date, 15 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Obesity known to be caused by monogenic mutations, other diseases, or medications.
  • Family or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2.
  • A history of moderate to severe depression at any time in the past or a score of ≥15 on the PHQ-9 questionnaire at screening; a history of bipolar disorder, schizophrenia, or other severe psychiatric disorders.
  • A history of organ transplantation (excluding corneal transplant), or being currently prepared to undergo organ transplantation.
  • Allergic constitution (allergic to multiple medications or foods), or those known to be allergic to RAY1225, GLP-1 receptor agonists, or GLP-1 related drugs.

Other

  • Plans to quit smoking during the study period

Who the study is looking for

  • Age ≥ 18 years.
  • Body mass index ≥ 28 kg/m2 or ≥24kg/m² to \<28 kg/m2 with at least 1 of the following weight-related comorbidities: a) Systolic blood pressure ≥130 mmHg or diastolic blood pressure ≥85 mmHg, or the use of at least one antihypertensive medication to maintain normal blood pressure;b) Fasting triglycerides (TG) ≥1.70 mmol/L, fasting low-density lipoprotein cholesterol (LDL-C) ≥4.1 mmol/L, fasting high-density lipoprotein cholesterol (HDL-C) \<1.04 mmol/L, or the need for at least one lipid-lowering treatment to maintain normal lipid levels; c) Obstructive sleep apnea syndrome; d) Fatty liver; e) Cardiovascular disease; e) Polycystic ovary syndrome.
  • History of at least 1 self-reported unsuccessful attempt at weight loss by diet and exercise.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University People's Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.