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NCT07801313CompletedPhase 1

Phase 1 Clinical Study of MWN105 Injection in Healthy Chinese Volunteers

A Randomized, Double-Blind, Placebo-Controlled Phase 1 Clinical Study to Evaluate the Safety, Tolerability, Immunogenicity, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Subcutaneous Ascending Doses of MWN105 Injection in Healthy Chinese Volunteers

Source: ClinicalTrials.gov · Last updated 3 Sept 2026

Brief summary (registry, in English)

This study is a randomized, double-blind, placebo-controlled, single-dose and multiple-dose, dose-escalation phase I clinical trial, aiming to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic characteristics, and immunogenicity of MWN105 injection in healthy Chinese volunteers, and to provide a reference for the next clinical trial. This study includes a single ascending dose (SAD) study and a multiple ascending dose (MAD) study. The SAD study consists of 4 dose groups; the MAD study consists of 2 dose groups and adopts a 4-week dose titration scheme. The study plans to enroll 55 volunteers. The primary endpoint is the incidence of adverse events. The secondary endpoints are the pharmacokinetic and pharmacodynamic characteristics and immunogenicity endpoints.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
55 (actual)
First submitted
31 Aug 2026
Start date
19 Dec 2024
Primary completion date
20 Jul 2025
Lead sponsor
Shanghai Minwei Biotechnology Co., Ltd
NCT number
NCT07801313

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 55
  • From 19 Dec 2024 to the primary completion date, 20 Jul 2025
  • 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

  • Those with clinically significant gastric emptying abnormalities (such as gastric outlet obstruction), severe chronic gastrointestinal diseases (such as having had active ulcers within 6 months), long-term use of drugs that directly affect gastrointestinal motility (including but not limited to mosapride, cispamide), or those who have undergone gastrointestinal surgery within 12 weeks before screening and are assessed by the investigator as not suitable to participate in this clinical study.
  • Used any prescription drugs, herbal medicines, over-the-counter drugs, or dietary supplements within 2 weeks before administration.
  • Had an infectious disease within 4 weeks before screening, severe trauma, or a history of major surgery.
  • Received vaccines or planned to receive vaccines during the trial screening.
  • Donated blood, experienced significant blood loss (\> 450 mL), or received a blood transfusion within 12 weeks before screening.

Other illness

  • Any history of clinical severe diseases or current presence of any clinically significant diseases.
  • Those with a known history or family history of medullary thyroid carcinoma, type 2 multiple endocrine neoplasia syndrome (MEN2), or those with a history of hypothyroidism or abnormal thyroid hormone levels.

Lab values

  • Subjects with a history of acute or chronic pancreatitis, symptomatic gallbladder disease, history of pancreatic injury, or other high-risk factors that may cause pancreatitis, or those with an amylase level \> 1.5 times the upper limit of the normal range (ULN) during screening.

Who the study is looking for

  • The selected subjects should be healthy male or female individuals aged 18 to 45 years (inclusive).
  • Female subjects should have a body weight of at least 50.0 kg, and male subjects should have a body weight of at least 55.0 kg. Their body mass index (BMI) should be within the range of 19.0-28.0 kg/m² (inclusive).
  • Physical examination, vital signs, 12-lead electrocardiogram (ECG), abdominal ultrasound, and clinical laboratory test results (including serum calcitonin, coagulation function, and thyroid function) should show no clinically significant abnormalities.
  • Subjects are required to abstain from sexual activity or use two effective contraceptive methods simultaneously starting from 1 month before screening through 6 months after the last administration, and must have no plans for sperm or egg donation.

Age in the registry: 18 years to 45 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
Hangzhou First People's Hospital
Coordinator of this site? Confirm its status
HangzhouChinaUnknown status

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