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Clinical Trials/NCT05166837
NCT05166837
Completed
Phase 1

A Randomized, Double-blind, Placebo-controlled, Single-ascending Dose Phase Ⅰa Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of STSA-1002Following Intravenous Infusion in Healthy Subjects

Staidson (Beijing) Biopharmaceuticals Co., Ltd5 sites in 1 country52 target enrollmentJanuary 10, 2022

Overview

Phase
Phase 1
Intervention
STSA-1002 injection
Conditions
Healthy
Sponsor
Staidson (Beijing) Biopharmaceuticals Co., Ltd
Enrollment
52
Locations
5
Primary Endpoint
Time of maximum concentration (Tmax)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

A randomized, double-blind, placebo-controlled, single-ascending dose Phase Ⅰa study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of STSA-1002 following intravenous infusion in healthy subjects

Registry
clinicaltrials.gov
Start Date
January 10, 2022
End Date
January 12, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Staidson (Beijing) Biopharmaceuticals Co., Ltd
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy subjects, aged ≥ 18 but ≤ 65, male and female;
  • Body mass index: 18.0 -25.0 kg/m2, inclusive;
  • Subjects (including their partners) agree to take highly effective contraceptive measures during the study, and they have no birth plan or sperm donation plan within 5 months after the end of the study;
  • Medical histories, physical examinations, laboratory examinations and study-related examinations and tests of the subjects show normal results or mild abnormalities with no clinical significance before enrollment, and the Investigator judges that they are eligible;
  • Subjects are aware of the risks of the study, and voluntarily participate in the clinical study and sign an informed consent form (ICF).

Exclusion Criteria

  • Past history of tuberculosis, history of contact with active tuberculosis, and positive tuberculin test results;
  • History of cardiovascular, respiratory, kidney, liver, metabolism, endocrine, gastrointestinal, blood, nerve, skin and mental illness, cancer or other major disease that in the judgment of the Investigator might put the subject as risk on this study;
  • There is a clear history of food or drug allergy or the total serum immunoglobulin IgE is higher than the upper limit of normal;
  • Positive screening test results for human immunodeficiency virus (HIV-1/HIV-2) antibodies, hepatitis B surface antigen (HBsAg) or hepatitis C antibody (HCVAb);
  • Presence of clinically significant vital signs values or of electrocardiogram (ECG) abnormalities during the screening period, as defined by an Investigator;
  • ANA positive;
  • During the screening period, the white blood cell count and C-reactive protein test results are abnormal and have clinical significance, hemoglobin: male \<120g/L or female \<110g/L;
  • Smoking more than 5 cigarettes per day or equivalent amount of tobacco in the 3 months before screening;
  • Subjects whose daily consumption of alcohol at the time of screening or at any time within the prior 6 months is more than 2 standard drinks, where 1 standard drink = 355 mL or 12 oz (1 can) of regular-strength (5%) beer; 150 mL or 5 oz wine; 45 mL or 1.5 oz liquor/spirits (40%);
  • Subjects who had a history of drug abuse or tested positive for drugs within 1 year before screening;

Arms & Interventions

Cohort 1:2mg/kg

All participants (fasted) received either 2 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: STSA-1002 injection

Cohort 1:2mg/kg

All participants (fasted) received either 2 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: Placebo

Cohort 2:5mg/kg

All participants (fasted) received either 5 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: STSA-1002 injection

Cohort 2:5mg/kg

All participants (fasted) received either 5 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: Placebo

Cohort 3:10mg/kg

All participants (fasted) received either 10 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: STSA-1002 injection

Cohort 3:10mg/kg

All participants (fasted) received either 10 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: Placebo

Cohort 4:20mg/kg

All participants (fasted) received either 20 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: STSA-1002 injection

Cohort 4:20mg/kg

All participants (fasted) received either 20 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: Placebo

Cohort 5:30mg/kg

All participants (fasted) received either 30 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: STSA-1002 injection

Cohort 5:30mg/kg

All participants (fasted) received either 30 mg/kg of STSA-1002 as a single dose or dose-matched placebo.

Intervention: Placebo

Outcomes

Primary Outcomes

Time of maximum concentration (Tmax)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Last measurable concentration (Clast)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Mean residence time (MRT)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Incidence of Adverse Events, Clinically Significant Laboratory Abnormalities, Clinically Significant Electrocardiogram Abnormalities, Clinically Significant Vital Signs Abnormalities And Clinically Significant Physical Examination Abnormalities.

Time Frame: 48 days

Elimination half-life (t1/2)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Apparent volume of distribution (Vz)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Maximum plasma concentration (Cmax)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Area under the plasma concentration-time curve from time 0 to the collection time point t of the last measurable concentration (AUC0-t)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Area under the plasma concentration-time curve from time 0 to infinity (AUC0-∞)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Clearance (CL)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Elimination rate constant of plasma drug concentration in terminal phase (λz)

Time Frame: Up to 1152 hours postdose

To evaluate the pharmacokinetics (PK) characteristics of STSA-1002 in healthy adult subjects

Secondary Outcomes

  • Change from baseline in concentration of free C5a and anti-drug antibody(Up to 1152 hours postdose)
  • Change from baseline in concentration of CH50, IL-6, IL-8,C4, TNF-α, IFN-γ(Up to 1152 hours postdose)

Study Sites (5)

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