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Completed

NCT Number: NCT07787624

Phase 1 Clinical Study of MWN109 Injection in Healthy Chinese Volunteers

This is a randomized, double-blind, placebo-controlled, single- and multiple- dose-escalating Phase 1a study. The objective is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of MWN109 Injection in healthy Chinese volunteers and to provide data for subsequent clinical trials.

The study includes a single ascending dose (SAD) part with 4 dose cohorts and a multiple ascending dose (MAD) part with 3 dose cohorts, using a 3-week dose titration regimen.

Approximately 58 volunteers will be enrolled. The primary endpoint is safety, assessed by adverse events, serious adverse events, vital signs, physical examinations, laboratory tests, and 12-lead electrocardiograms. The secondary endpoint is the pharmacokinetic characteristics.

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Key information

Conditions

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

The First Affiliated Hospital of Yunnan University of Chinese Medicine (Yunnan Provincial Hospital of Traditional Chinese Medicine)

Kunming, Yunnan, China

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female participants aged 18 to 65 years (inclusive) at the time of signing the informed consent form (ICF); the proportion of either gender shall not be less than 1/3.
  • Male participants with body weight not less than 50 kg, female participants with body weight not less than 45 kg; body mass index (BMI) within 20.0 to 40.0 kg/m^2 (inclusive).
  • Female participants must have no plans for pregnancy or egg donation from 14 days before the first dose to 6 months after the last dose and must agree to use effective contraceptive measures to avoid pregnancy; male participants must have no plans for fathering a child or sperm donation from the first dose to 6 months after the last dose and must agree to use effective contraceptive measures to avoid causing partner pregnancy.

Exclusion criteria

  • History of severe drug allergy (especially known or suspected allergy to the excipients of MWN109 Injection) or severe atopic allergic diseases/history (asthma, urticaria, eczematous dermatitis, etc.) or severe allergic constitution (allergy to two or more foods or drugs) (by inquiry).
  • History of acute or chronic pancreatitis, symptomatic gallbladder disease, pancreatic injury or other high-risk factors that may lead to pancreatitis, or serum amylase > 1.5 × upper limit of normal (ULN) at screening (by inquiry and examination).
  • Family history or history of medullary thyroid C-cell tumor/carcinoma; history of thyroid dysfunction or abnormal thyroid hormone levels (by inquiry).
  • History or presence at screening of digestive system diseases that may increase the risk to volunteers, such as pancreatitis, abnormal gastric emptying (e.g., gastroparesis, pyloric stenosis, pyloric obstruction, etc.), or severe chronic gastrointestinal diseases (e.g., history of intestinal obstruction, active ulcer within 6 months) (by inquiry).
  • History of infectious diseases (which, in the investigator's assessment, may significantly affect the safety evaluation of volunteers) or severe trauma within 4 weeks before screening, or major surgery within 3 months before screening (by inquiry and examination).
  • Use of any prescription or over-the-counter drug (including chemical drugs, vitamins, herbal medicines, etc.) within 2 weeks before dosing (by inquiry and examination);
  • History of substance abuse (by inquiry).
  • Blood donation or massive blood loss (> 400 mL) or blood transfusion within 3 months before screening (by inquiry).

Treatment and study plan

MWN109

Drug

S1, S2 S3, S4; administered subcutaneously (SC)

Placebo

Drug

administered SC

Primary outcomes

  1. Incidence of adverse events (AEs)

    Time frame: From Day 1 to Day 43

    The incidence of adverse events (AEs) and serious adverse events (SAEs).

Secondary outcomes

  1. Maximum Concentration (Cmax)

    Time frame: From Day 1 to Day 29

    Cmax of MWN109.

  2. Time to Reach Maximum Concentration (Tmax)

    Time frame: From Day 1 to Day 29

    Tmax of MWN109.

  3. Area Under the Curve From Time 0 to Last Quantifiable Time Point (AUC0-t)

    Time frame: From Day 1 to Day 29

    AUC0-t of MWN109.

  4. Area Under the Curve From Time 0 to Infinity (AUC0-inf)

    Time frame: From Day 1 to Day 29

    AUC0-inf of MWN109.

  5. Elimination Half-Life (t1/2)

    Time frame: From Day 1 to Day 29

    t1/2 of MWN109.

  6. Steady State Maximum Concentration (Cmax,ss)

    Time frame: From Day 1 to Day 43

    Cmax,ss of MWN109.

  7. Steady State Minimum Concentration (Cmin,ss)

    Time frame: From Day 1 to Day 43

    Cmin,ss of MWN109.

  8. Steady State Concentration (Cav,ss)

    Time frame: From Day 1 to Day 43

    Cav,ss of MWN109.

  9. Time to Reach Maximum Concentration at Steady State (Tmax,ss)

    Time frame: From Day 1 to Day 43

    Tmax,ss of MWN109.

  10. Steady State Apparent Terminal Elimination Half-life (t1/2,ss)

    Time frame: From Day 1 to Day 43

    t1/2,ss of MWN109.

  11. Area Under Concentration-time Profiles during a Dose Interval (AUC0-τ,ss)

    Time frame: From Day 1 to Day 43

    AUC0-τ,ss of MWN109.

  12. Steady State Area Under the Curve From Time 0 to Last Quantifiable Time Point (AUC0-t,ss)

    Time frame: From Day 1 to Day 43

    AUC0-t,ss of MWN109.

Sponsors and collaborators

Lead sponsor

Shanghai Minwei Biotechnology Co., Ltd

Industry

Registry information

Official study title

A Randomized, Double-Blind, Placebo-Controlled Phase 1a Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Single and Multiple Subcutaneous Dose Escalation of MWN109 Injection in Healthy Chinese Volunteers

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Aug 26, 2026
Registry last updated
Aug 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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