Evaluation of the Safety, Tolerability and Pharmacokinetics of HY8931 in Healthy Adult Participants

NCT07281703 | Recruiting Phase 1

• 1 other identifier: HY8931-01-01
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this clinical trial is to learn the safety, tolerability and pharmacokinetics of single and multiple doses of HY8931 in healthy adult participants. The main questions it aims to answer are:

• How is the safety and tolerability following administration of single and multiple doses of HY8931 in healthy adult participants?
• What is the PK character of HY8931 following administration of single and multiple doses of HY8931 in healthy adult participants? Researchers will compare HY8931 to a placebo (a look-alike substance that contains no drug) to see if HY8931 is safe and well tolerated. Participants will take HY8931 or a placebo once or twice in single dose group or multiple dose group. And will be follow-up until Day 90.

Conditions

Healthy

Outcome Measures

Primary Outcomes (1)

• Number of Participants with Treatment-Related Adverse Events as Assessed by CTCAE v5.0

  From signing informed consent form to the end of study at Day 90.

Secondary Outcomes (4)

• Peak Plasma Concentration (Cmax)

  From Day1 predose to Day 90.

• Area under the plasma concentration versus time curve (AUC)

  From Day1 predose to Day 90.

• Time to maximum concentration (Tmax)

  From Day1 predose to Day 90.

• Plasma half-life time (T1/2)

  From Day1 predose to Day 90.

Study Arms (2)

HY8931

EXPERIMENTAL

It's an injection solution. SAD part for intravenous dosing in 6 cohorts, including 10mg, 30mg, 60mg, 120mg, 240mg and 360mg with only one administration on Day 1 of each cohort. SAD part for subcutaneous dosing in 120mg cohort with only one administration on Day 1; MAD part for subcutaneous dosing in 3 cohorts, including 120mg, 240mg, 360mg with two administrations on Day 1 and Day 30 of each cohort.

Biological: HY8931

placebo

PLACEBO COMPARATOR

It's same injection solution just without active ingredient compared with HY8931. SAD part for intravenous dosing in 6 cohorts, including 10mg, 30mg, 60mg, 120mg, 240mg and 360mg with only one administration on Day 1 of each cohort. SAD part for subcutaneous dosing in 120mg cohort with only one administration on Day 1; MAD part for subcutaneous dosing in 3 cohorts, including 120mg, 240mg, 360mg with two administrations on Day 1 and Day 30 of each cohort.

Other: Placebo Control

Interventions

HY8931 BIOLOGICAL

HY8931 is an injection solution with 125mg/ml per vial. SAD part for intravenous dosing in 6 cohorts, including 10mg, 30mg, 60mg, 120mg, 240mg and 360mg and for subcutaneous dosing in 1 cohort of 120mg with only one administration on Day 1 of each cohort. MAD part for subcutaneous dosing in 3 cohorts, including 120mg, 240mg and 360mg with two administrations on Day 1 and Day 30 of each cohort.

HY8931

Placebo Control OTHER

A vial with 1ml injection solution contain same ingredient except HY8931 compared with HY8931 solution.

placebo

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Male and female participants must be 18 to 45 years of age, inclusive, at the time of signing the informed consent.
• Male and female participants who are overtly healthy as determined by medical evaluation including medical history, physical examination, laboratory tests, vital sign and 12-lead ECG.
• Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures.
• BMI of 18 to 32 kg/m2; and a total body weight \>50 kg.
• Capable of giving signed informed consent as described in Appendix 1, which includes compliance with the requirements and restrictions listed in the informed consent and in this protocol.

You may not qualify if:

• Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurological, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at the time of dosing).
• Positive hepatitis B surface antigen (HBsAg), hepatitis B core antibody (HBcAb), or hepatitis C antibody or positive testing for HIV or syphilis at the screening visit.
• History of allergic or anaphylactic reaction to a therapeutic drug.
• History of recent active infections within 28 days prior to the screening visit.
• Participants with a fever within 48 hours prior to dosing.
• Positive QFT-G test.
• History of recurrent bacterial infection (\>3 per year) or recurrent HSV infection.
• Recent exposure to live vaccines within 28 days of the screening visit or plan to receive live vaccination during the trial.
• Known exposure to anti-TL1A or IL23 or any type of anti-TL1A or anti-IL23 therapy.
• Previous administration with an investigational drug within 90 days (or as determined by the local requirement) or 5 half-lives preceding the first dose of study intervention used in this study (whichever is longer).
• A positive urine drug test.
• A positive pregnancy test.
• Screening supine BP ≥140 mm Hg (systolic) or ≥90 mm Hg (diastolic), following at least 5 minutes of supine rest. If BP is ≥140 mm Hg (systolic) or ≥90 mm Hg (diastolic), the BP should be repeated 2 more times and the average of the 3 BP values should be used to determine the participant's eligibility.
• Baseline 12-lead ECG that demonstrates clinically relevant abnormalities that may affect participant safety or interpretation of study results (eg, baseline QTc interval\>450 msec, complete LBBB, signs of an acute or indeterminate-age myocardial infarction, ST-T interval changes suggestive of myocardial ischemia, second or third-degree AV block, or serious bradyarrhythmias or tachyarrhythmias). If the baseline uncorrected QT interval is \>450 msec, this interval should be rate corrected- using the Fridericia method and the resulting QTcF should be used for decision making and reporting. If QTc exceeds 450 msec, or QRS exceeds 120 msec, the ECG should be repeated 2 more times and the average of the 3 QTc or QRS values should be used to determine the participant's eligibility. Computer interpreted-ECGs should be overread by a physician experienced in reading ECGs before excluding participants.
• Participants with ANY of the following abnormalities in clinical laboratory tests at screening, as assessed by the study specific-laboratory and confirmed by a single repeat test, if deemed necessary:

Sponsors & Collaborators

• Newsoara Biopharma Co., Ltd.: lead

Study Sites (1)

Q-Pharm Pty Ltd.

Brisbane, Australia

RECRUITING

Study Officials

• Weifen Zhou, Dr.

  Newsoara Biopharma Co., Ltd.

  STUDY DIRECTOR

Central Study Contacts

Vandy Xu

CONTACT

+8613651674576; vandy.xu@newsoara.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 19, 2025
• First Posted: December 15, 2025
• Study Start: January 14, 2026
• Primary Completion (Estimated): September 1, 2026
• Study Completion (Estimated): October 1, 2026
• Last Updated: March 11, 2026

Record last verified: 2025-12

Data Sharing

• IPD Sharing: Will not share

Locations

AU (1)