A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of SSS39 Injection in Healthy Chinese Subjects

NCT ID: NCT07057726

Last Updated: 2025-07-10

Basic Information

• Recruitment Status: ENROLLING_BY_INVITATION
• Clinical Phase: PHASE1
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-10-09
• Study Completion Date: 2025-10-31

Brief Summary

To evaluate the safety, tolerability, and pharmacokinetics of SSS39 injection in healthy Chinese subjects

Detailed Description

This study was a single-administration, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, PK profile, immunogenicity, and effects on Treg cells and cytokines of SSS39 injection in healthy individuals.

Conditions

Safety and Tolerability in Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: TRIPLE

Study Groups

group 1

Low-dose Group

Group Type: EXPERIMENTAL

SSS39

Intervention Type: DRUG

Single oral administration of SSS39

group 2

high dose Group

Group Type: EXPERIMENTAL

SSS39

Intervention Type: DRUG

Single oral administration of SSS39

Interventions

SSS39

Single oral administration of SSS39

Intervention Type: DRUG

SSS39

Single oral administration of SSS39

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• 1. Healthy subjects aged 18-45 years old (including boundary values), regardless of gender;
• 2. Subjects voluntarily participate in clinical trials and sign informed consent;
• 3. Male weight ≥50 kg, female weight ≥45 kg, body mass index (BMI) between 19-28 kg/m2 (including the cut-off value);

Exclusion Criteria

• 1.Have a clear history of drug or food allergy, or are known to have an allergic reaction to Sirolimus, polyethylene glycol and any excipients of this product, including lactose intolerance;
• 2.Subjects who have received any other drug that acts on the mammalian target protein of rapamycin (mTOR);
• 3. within 14 days prior to administration of the investigational product (or five half-lives of CYP3A4/P-gp inhibitors/inducers, whichever is longer), or anticipated use of a known major CYP3A4/P-gp inhibitor or major CYP3A4/P-gp inducer (including natural products) during the trial, Such as St. John's wort or grapefruit juice);
• 4.Abnormal results of sedimentation, abdominal B-ultrasonography, kidney B-ultrasonography or superficial lymph node B-ultrasonography during the screening period were judged by researchers to be clinically significant;
• 5. Acute or chronic systemic infection or local infection within 2 weeks before screening;
• 6. Previous or current history of autoimmune disease, immune deficiency, or history of organ transplantation, or/and use of immunomodulatory or immunosuppressive drugs within 6 months prior to screening;
• 7. Those who have had major surgery or have not fully recovered from any previous invasive procedure within 4 weeks prior to dosing;
• 8. Have syphilis (positive for treponema pallidum antibodies) or AIDS (positive for HIV antibodies), or active hepatitis C (positive for hepatitis C virus antibodies and positive for hepatitis C virus [HCV]RNA results), or active hepatitis B (positive for hepatitis B surface antigen and hepatitis B virus [HBV] DNA above the lower limit of quantitative values);
• 9. Patients with past or present history of any clinically serious diseases, including but not limited to digestive system, cardiovascular system, respiratory system, urinary system, musculoskeletal system, endocrine system, neuropsychiatric system, blood system, etc. (except those considered by researchers to be eligible for inclusion);
• 10. Past or present history of malignant tumors;
• 11. Use of any drug (including prescription, over-the-counter, Chinese herbal, etc.) or supplement within 2 weeks prior to administration (if determined by the investigator, the time interval between the drug used and the beginning of administration of this trial > 5 half-lives, corresponding subjects can also be enrolled);
• 12. Those who received live vaccines within 1 month before administration or planned to receive live vaccines during the study period, including but not limited to: measles, mumps, rubella, chickenpox, yellow fever, rabies, BCG, typhoid vaccine, etc.;
• 13.Previous alcohol abuse or regular alcohol consumption in the 6 months prior to the test (drinking more than 14 units of alcohol per week, 1 unit =360 mL beer or 45 mL spirits with 40% alcohol or 150 mL wine) or a positive alcohol breath test (breath alcohol content > 0.0 mg/100 mL), or those who cannot abstain from alcohol during the trial;
• 14.Those who test positive for one or more drug addiction and drug abuse tests, or have a history of drug abuse/dependence or drug abuse within the previous year;
• 15. habitual excessive consumption of tea, coffee or caffeinated beverages (more than 8 cups a day, 1 cup =200 mL), and/or ingestion of any food or beverage containing caffeine, alcohol, xanthine and other ingredients (such as coffee, strong tea, chocolate, etc.) within 48 hours before administration;
• 16.Smokers who smoked more than 5 cigarettes per day in the 3 months before screening and those who could not smoke during the whole test period;
• 17. Participants who have participated in any drug clinical trial and taken experimental drugs, or participated in device clinical trial and used experimental devices within 3 months before screening;

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Shenyang Sunshine Pharmaceutical Co., LTD.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

SSS39

Beijing, , China

Countries

China

Other Identifiers

SYSS-SSS39-UND-I-01

Identifier Type: -

Identifier Source: org_study_id