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NCT06350812CompletedPhase 1/2

A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of PB-119 Injection in Chinese Obese Subjects

A Single-center, Randomized, Double-blind, Placebo-controlled, Multiple Dose Escalating Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of PB-119 Injection in Chinese Obese Subjects

Source: ClinicalTrials.gov · Last updated 19 Nov 2025

Brief summary (registry, in English)

The trial is conducted in a single-center, randomized, double-blind, placebocontrolled, dose-increasing design. To evaluate the safety, tolerability, pharmacokinetics(PK) characteristics, efficacy and immunogenicity of PB-119 injection in Chinese obese subjects.

Status (registry)
Completed
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
32 (actual)
First submitted
18 Mar 2024
Start date
27 May 2024
Primary completion date
16 Nov 2024
Lead sponsor
PegBio Co., Ltd.
Diseases
Obesity
NCT number
NCT06350812

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 32
  • From 27 May 2024 to the primary completion date, 16 Nov 2024
  • 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.

Prior treatment

  • Diagnosed cardiovascular and cerebrovascular diseases with obvious clinical significance within 6 months before screening
  • Use of any approved or unapproved drugs or products that have an effect on body weight within 3 months prior to screening

Other illness

  • History of Cushing's syndrome, polycystic ovaries, or other hereditary endocrine disorders, or obesity caused by secondary factors such as cortisol hormones.
  • History of multiple endocrine neoplasia syndrome type 2 (MEN-2) , medullary thyroid carcinoma (MTC) or Category 4 and above thyroid nodules by Thyroid ultrasound Chinese Ultrasound Thyroid Imaging Reporting and Data System (C-TIRADS)
  • History of bariatric surgery for weight loss before screening.

Lab values

  • Fasting Plasma Glucose(FPG) ≥7.0mmol/L or glycosylated hemoglobin (HbA1c) ≥6.5% or diagnosed diabetes
  • FPG \<3.9 mmol/L at screening and/or a history of hypoglycemia.
  • Abnormal Thyroid-Stimulating hormone(TSH), Serum Free Triiodothyronine(FT3), Serum Free Thyroxine(FT4) or diagnosed thyroid dysfunction
  • Time history from the starting point of P-wave to the starting point of QRS wave(PR intervals )\> 210 msec and/or QRS complex(QRS) \> 120 msec and/or Corrected QT Interval(QTcF) \> 450 msec at screening or randomization.
  • Serum amylase or lipase \> 3× upper limit of normal (ULN) at screening or before randomization, or previously diagnosed acute/chronic pancreatitis.
  • Low density lipoprotein cholesterol(LDL-C) ≥4.40 mmol/L or triglyceride (TG) ≥5.65 mmol/L.

Other

  • Systolic blood pressure \> 160 mmHg and/or diastolic blood pressure \> 100 mmHg at screening or randomization.

Who the study is looking for

  • Chinese male or female subjects aged 18-60 years (both inclusive).
  • Body weight ≥70 kg(male) or 60 kg(female), and body mass index (BMI)
    • ≥30.0 kg/m2 at screening.
  • Weight change \<5% in the past 3 months before screening.

Age in the registry: 18 years to 60 years · Sex: All · Accepts 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
The Third Xiangya Hospital of Central South University
Coordinator of this site? Confirm its status
ChangshaChinaUnknown status

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