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Overweight or ObesityPhase 1NCT07776041

A Study of SYH2092 Injection in Healthy Participants

A Phase 1 study testing SYH2092 Injection in people with Overweight or Obesity, run by CSPC Megalith Biopharmaceutical Co.,Ltd. at 1 site in Australia.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

To evaluate the safety and tolerability of SYH2092 Injection in healthy participants Read more about this study

Who is it for?
Ages 18 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Overweight or Obesity
What is being tested?
SYH2092 Injection
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
46 participants
Where
1 siteAustralia
Study dates
30 Sep 2026to 20 Apr 2027
Phase
Phase 1
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Fully understand the content, process and possible adverse drug reactions (ADRs) of the study before the study, and voluntarily sign the ICF;
  • At Screening, aged 18 to 60 years (inclusive, based on the date of signing the ICF), including both males and females;
  • At Screening, body weight ≥ 50 kg with a body mass index (BMI) of 18 to 35 kg/m²
  • Body weight change ≤ 5% within 3 months prior to Screening (including the Screening Period) (based on participant self-report);
  • Participants (including their partners) have no birth plan from signing the ICF until 6 months after the last dose, and agree to use highly effective contraceptive measures as stipulated in the protocol.

Who cannot join

  • Known or suspected allergy to amylin receptor agonists or any component of the investigational product; or those with an allergic constitution (allergy to multiple drugs and foods);
  • Clinically significant abnormal results in vital signs, physical examination, laboratory tests, or ECG, as judged by the Investigator, that render the participant unsuitable for the study. The following conditions do not lead to exclusion: (1) TG ≤ 3.42 mmol/L, TC ≤ 7.5 mmol/L, HDL-C abnormal; (2) alanine aminotransferase (ALT) < 1.5 × upper limit of normal (ULN), aspartate aminotransferase (AST) < 1.5 × ULN, or total bilirubin <1.5 × ULN;
  • HbA1c ≥ 6.5% during Screening Period, or fasting glucose < 3.9 mmol/L or ≥ 7 mmol/L;
  • Prolonged QTcF interval during Screening Period (≥ 450 ms for males; ≥ 460 ms for females; see Section 13.5 for calculation formula), history of risk factors for Torsades de Pointes (e.g., cardiac failure/cardiomyopathy, or family history of long QT syndrome);
  • Positive for any of the following: Hepatitis B surface antigen, hepatitis C virus antibody, human immunodeficiency virus antibody, or Treponema antibody.
  • Significant history or clinical manifestation of any metabolic, dermatological, hepatic, renal, hematological, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, immune or psychiatric disorder that, in the opinion of the Investigator, may place the participant at increased risk or interfere with study assessments. This does not include: resolved childhood asthma; mild intermittent asthma; seasonal allergic rhinitis; eczema with no use of topical steroid creams within 3 months prior to Screening; fully resolved gestational diabetes; or Gilbert's syndrome;
  • Severe trauma or major surgery within 3 months prior to Screening, or plan to undergo surgery during the study; 8)History of malignancy (not including basal cell carcinoma [BCC], squamous cell carcinoma [SCC], or carcinoma in situ of the cervix); history of severe/major depressive/anxiety (not including history of mild/resolved depressive/anxiety, as judged by the Investigator); or epilepsy (not including a history of febrile seizures in childhood);
  • 9) History of clinical gastric emptying abnormalities (e.g., gastric outlet obstruction) or severe chronic gastrointestinal diseases (e.g., inflammatory bowel disease, active ulcers); history of acute or chronic pancreatitis; or active/current gallbladder disease (e.g., symptomatic cholelithiasis, cholecystitis). This does not include a history of cholecystectomy for resolved gallbladder disease; 10) History of gastrointestinal surgery that may lead to malabsorption, or long-term use of drugs directly affecting gastrointestinal motility, or other therapies that affect gastrointestinal motility. Examples include: bariatric surgery or procedures (e.g., gastric banding), or use of glucagon-like peptide-1 (GLP-1) receptor agonist, glucose-dependent insulinotropic polypeptide (GIP) receptor agonist, amylin receptor agonists, or drugs/products deemed by the Investigator to cause body weight changes and affect body weight assessment within 3 months prior to Screening (see Section 6.8 for details); This does not include appendectomy or uncomplicated hernia repair, which are permitted; 11) Presence of symptoms or signs of dermatitis or skin abnormalities (including tattoos) at or around the injection site (abdomen), or within 5 cm of the injection site; 12) Use of any prescription drugs within 14 days prior to dosing, or less than 5 half-lives have elapsed since the last use (whichever is longer), with the exception of hormonal contraceptives used for contraceptive purposes as permitted under Section 13.1.2; Use of any over-the-counter (OTC) drugs (excluding topical medications such as creams, ointments, or eye drops), dietary supplements, or herbal medicines within 7 days prior to dosing, or less than 5 half-lives have elapsed since the last use (whichever is longer), except for short-term use of paracetamol and anti-inflammatory drugs within 7 days prior to dosing, at the Investigator's discretion; 13)Use of drugs that may affect glucose metabolism (e.g., systemic steroids, non-selective beta-blockers, monoamine oxidase inhibitors) within 1 month prior to Screening, or less than 5 half-lives have elapsed since the last use of such drugs (whichever is longer); 14) Average weekly alcohol consumption exceeding 21 units (males) or 14 units (females) within 3 months prior to Screening (1 unit ≈ 360 mL of beer with 5% alcohol content, or 45 mL of spirits with 40% alcohol content, or 150 mL of wine with 12% alcohol content), positive breath alcohol test, or inability to abstain from alcohol during the study; 15)Participants who smoked > 10 cigarettes/week or 2 cigarettes/day (or nicotine-equivalent, including e-cigarettes/vaping devices) within 3 months prior to Screening or who cannot stop using any nicotine products (including cigarettes, e-cigarettes/vaping devices, smokeless tobacco, and nicotine replacement therapy) during the study. A positive cotinine result, or the need for repeat testing, may be permitted at the Investigator's discretion; 16) Average daily consumption of excessive tea, coffee, and/or caffeine-containing beverages (more than 8 cups on average, 1 cup ≈ 250 mL) within 3 months prior to Screening, or inability to abstain during the study; 17) Strenuous exercise (e.g., weightlifting, sprinting, long-distance running, cycling, swimming, soccer) within 48 h prior to Screening; 18) History of drug abuse within 3 months prior to Screening, or positive drug abuse screening test. A positive drug abuse screening test result attributable to a documented medical history of prescribed medication may be permitted at the Investigator's discretion, following discussion with the Sponsor, provided the participant is not currently receiving such medication; 19) Has donated whole blood or had a loss of whole blood of more than 500 mL within the 30 days prior to Screening; has donated plasma (plasmapheresis) within 7 days prior to Screening; or has received a blood transfusion within one year prior to Screening; Participants with a history of needle phobia and blood phobia, difficulty in blood collection or intolerance to venipuncture blood collection; 21) Participants who had special dietary requirements and could not accept a uniform diet and rest. The following dietary requirements will be accommodated: dairy/lactose-free, gluten-free, gluten-free and lactose-free, halal, no pork and beef, no red meat, no seafood, pescatarian, standard, vegan, and vegetarian; 22) Females who are pregnant, lactating, or have a positive serum pregnancy test during the Screening Period; 23) Participation in any other clinical study of drugs or medical devices within 3 months or 5 half-lives prior to Screening (whichever is longer), or planned participation in a clinical study of other drugs or medical devices during this study; 24) Participants whom the Investigator judges to have other factors that make them unsuitable to participate in the trial.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Clinical Trials Information Group NA officer contact

86-0311-69085587

ctr-contact@cspc.cn

Australia1 site
  • Nucleus Network Pty Ltd.

    Melbourne, Victoria, 3004

    Philip John Ryan, +61 3 8593 9801, p.ryan@nucleusnetwork.com.au

Other trials in Australia

About this study

To evaluate the safety and tolerability of SYH2092 Injection in healthy participants

Being tested
SYH2092 Injection, Placebo
Medical subject headings
Overweight, Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • SYH2092 InjectionDrug

    Conduct in accordance with the study protocol.

  • PlaceboDrug

    Conduct in accordance with the study protocol.

Study groups in NCT07776041
Study groupRoleWhat they receive
SYH2092 InjectionExperimentalNot described
Receives: Drug: SYH2092 Injection
PlaceboPlacebo comparatorNot described
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of participants with treatment-related adverse events as accessed by CTCAE v6.0

    Measured: Screening period up to day 71

Secondary outcomes (21)
  1. Maximum plasma concentration (Cmax)

    Measured: predose on day 1 to day 71

  2. Area under the concentration-time curve from time 0 to the last measurable time point (AUClast)

    Measured: predose on day 1 to day 71

  3. Area under the concentration time curve from time 0 to infinity (AUCinf)

    Measured: predose on day 1 to day 71

  4. Percent of AUC extrapolated to infinity (AUC_Extrap)

    Measured: predose on day 1 to day 71

  5. Time to maximum concentration (Tmax)

    Measured: predose on day 1 to day 71

  6. Elimination half-life (t1/2)

    Measured: predose on day 1 to day 71

  7. Apparent volume of distribution (Vz/F)

    Measured: predose on day 1 to day 71

  8. Apparent clearance (CL/F)

    Measured: Predose on day 1 to day 71

  9. Mean change in plasma glucose from baseline

    Measured: baseline up to day 71

  10. Mean change in insulin from baseline

    Measured: baseline up to day 71

  11. Mean change in C-peptide from baseline

    Measured: baseline up to day 71

  12. Mean change in glucagon from baseline

    Measured: baseline up to day 71

  13. Mean change in HbA1c from baseline

    Measured: baseline up to day 71

  14. Change in body weight from baseline

    Measured: baseline up to day 71

  15. Change in waist circumference from baseline

    Measured: baseline up to day 71

  16. Mean change in Total Cholesterol(TC) from baseline

    Measured: baseline up to day 71

  17. Mean change in Triglycerides(TG) from baseline

    Measured: baseline up to day 71

  18. Mean change in Low-Density Lipoprotein Cholesterol(LDLC) from baseline

    Measured: baseline up to day 71

  19. Mean change in High-Density Lipoprotein Cholesterol(HDLC) from baseline

    Measured: baseline up to day 71

  20. Incidence and titer of anti-drug antibody (ADA)

    Measured: predose on day 1 to day 71

  21. Fridericia-corrected QT interval (QTcF)

    Baseline- and placebo-adjusted corrected QTcF

    Measured: baseline up to day 8

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Aug 2026
  2. Study start30 Sep 2026 (estimated)
  3. Primary completion9 Feb 2027 (estimated)
  4. Study completion20 Apr 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
NA (not mandatory)
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
46 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07776041
Sponsor's protocol ID
SYH2092-002
Status last verified
Aug 2026
First submitted
17 Aug 2026
Last updated
20 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing SYH2092 Injection in people with Overweight or Obesity, run by CSPC Megalith Biopharmaceutical Co.,Ltd. at 1 site in Australia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 20 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Australia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Clinical Trials Information Group NA officer (86-0311-69085587, ctr-contact@cspc.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of participants with treatment-related adverse events as accessed by CTCAE v6.0 (time frame: Screening period up to day 71). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2026.

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