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Study identifier: NCT07616037 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Efficacy of a GLP-1/FGF21 Dual Agonist for Treating PCOS

Condition: PCOS (Polycystic Ovary Syndrome)  ·  Sponsor: Shanghai Zhongshan Hospital

PhasePhase 2
Planned participants30
Who can joinFemale, 18 Years to 40 Years
Healthy volunteersNo

About this study

Polycystic ovary syndrome (PCOS) is the most common reproductive endocrine and metabolic disorder among women of reproductive age. It is characterized by oligo-ovulation or anovulation, clinical and/or biochemical hyperandrogenism, and polycystic ovarian morphology. In addition, PCOS is frequently accompanied by multiple metabolic abnormalities, including insulin resistance, obesity, impaired glucose tolerance, and dyslipidemia. Clinical studies have demonstrated that treatment with glucagon-like peptide-1 receptor agonists (GLP-1RAs) in women with PCOS results in significant weight reduction, decreased free testosterone levels, improvement in menstrual regularity, and increased clinical pregnancy rates. Fibroblast growth factor 21 (FGF21) has been shown to enhance insulin sensitivity, promote fatty acid oxidation, and improve lipid distribution. HEC88473 is a novel long-acting dual agonist targeting both the glucagon-like peptide-1 (GLP-1) receptor and the fibroblast growth factor 21 (FGF21) receptor. This study is initiated to evaluate the clinical efficacy of HEC88473 in women with PCOS and to explore its potential as a new therapeutic option for the management of PCOS.

This description comes directly from the study's public registry record.

Talk to the study team

Jingjing JIANG, MD, PhD  ·  86-021-64041990  ·  jiang.jingjing@zs-hospital.sh.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Zhongshan Hospital, Fudan UniversityShanghai, Shanghai Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07616037