A Trial to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Profile of TNM005 in Healthy Adult Subjectsy
- Registration Number
- NCT06068608
- Lead Sponsor
- Zhuhai Trinomab Pharmaceutical Co., Ltd.
- Brief Summary
The purpose of this clinical trial is to evaluate the safety and tolerability of TNM005 following a single dose by intramuscular (IM) administration in healthy adult subjects The main questions it aims to answer are:1. safety profile；2. PK properties 3. PD properties
- Detailed Description
This is a randomized, double-blind, placebo-controlled, single ascending dose, phase 1 study designed to evaluate the safety, tolerability, PK, PD (anti-VZV antibody level), and immunogenicity of TNM005, as well as to characterize the PD of VARIZIG, in healthy adult volunteers.
The study also includes a cohort in which eight subjects will receive a single dose of VARIZIG 625 IU. This cohort will be conducted in an open-label fashion and may be initiated as early as the first TNM005 cohort is dosed.
The study include periods of Screening (up to 28 days), in-patient (treatment on Day 1), and safety follow-up until Day 120.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 48
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- Signed and dated written informed consent;
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- Are willing and able to comply with scheduled visits, blood sampling, laboratory tests, and other study procedures;
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- Healthy males or females, 18-55 years of age (both inclusive);
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- Body mass index (BMI) within 18.5-31.0 kg/m2 (both inclusive) and body weight ≥50.0 kg for males and ≥45.0 kg for females;
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- Have no clinically significant abnormality on physical examination, vital signs, 12-lead ECG, and clinical laboratory tests as determined by the Investigator;
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- Females must be either surgically sterile or under post-menopausal status at Screening or agree to use a highly effective method of contraception from screening until 120 days after IMP dosing. In addition, males who are sexually active and partners of women of childbearing potential must agree to use effective contraception from screening until 120 days after drug administration.
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- History or evidence of any other acute or chronic disease that, in the opinion of the Investigator, may interfere with the evaluation of the safety or immunogenicity of the drug or compromise the safety of the subject;
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- History of surgery (except minor outpatient surgery) within three months prior to screening or planned surgery during the study;
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- History of receiving monoclonal antibody, immunoglobulin, or blood products within six months prior to dosing;
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- Receipt of systemic immunosuppressive medications;
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- Exposure to any live attenuated vaccine within four weeks prior to drug administration;
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- History of receiving vaccine(s) against zoster;
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- Use of any other drug, including over-the-counter medications, and herbs, within 14 days prior to the drug administration or five half-lives of the drug, whichever is longer, except for contraceptive medication in women of childbearing potential (WOCBP), or concomitant medications that are considered necessary for the subject's welfare and unlikely to interfere with the study;
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- Donated blood >400 mL or significant blood loss equivalent to 400 mL within one month before Screening; or plasma donation within 14 days before Screening; or any plan of blood or blood product donation during the study;
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- Positive test at a screening of any of the following: hepatitis B surface antigen (HBsAg), hepatitis C (HCV) antibody, or human immunodeficiency virus (HIV) antigen/antibody;
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- Known or suspected history of drug abuse within the past five years or with a positive urine drug test at Screening or on Day -1;
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- History of significant alcohol abuse within six months prior to screening or any indication of regular use of more than 14 units of alcohol per week or taking a product containing alcohol two days prior to dosing, or having a positive alcohol breath test on Day -1;
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- Use of ≥five cigarettes or equivalent nicotine-containing product per day on average over three months prior to Screening; or unwilling to refrain from nicotine products during study participation;
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- History of allergic or anaphylactic reaction to a therapeutic or diagnostic monoclonal antibody or IgG-fusion protein;
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- History of allergic or anaphylactic reaction to blood products (only for VARIZIG cohort);
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- IgA deficient subjects at risk for hypersensitivity reaction (only for VARIZIG cohort);
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- Subjects at high risk for thrombotic events, including those with a history of venous or arterial thrombosis, atherosclerosis, or multiple cardiovascular risk factors (only for VARIZIG cohort);
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- Participation in any other clinical studies with chemical or biological drugs or devices within four weeks or five times the half-life of the specific drug/biologics (whichever is longer) before drug administration;
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- Nursing mothers or pregnant women;
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- Subjects considered unsuitable for participating in the study in the opinion of the Investigator.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description TNM005 dose level 2/placebo Placebo TNM005 on different dose level 2 /placebo TNM005 level 3/placebo Placebo TNM005 on dose level 3 /placebo TNM005 dose level 5/placebo Placebo TNM005 on dose level 5 /placebo TNM005 dose level 1/placebo TNM005 TNM005 on dose level 1 /placebo TNM005 dose level 4/placebo TNM005 TNM005 on dose level 4 /placebo TNM005 dose level 1/placebo Placebo TNM005 on dose level 1 /placebo TNM005 dose level 2/placebo TNM005 TNM005 on different dose level 2 /placebo TNM005 level 3/placebo TNM005 TNM005 on dose level 3 /placebo TNM005 dose level 4/placebo Placebo TNM005 on dose level 4 /placebo TNM005 dose level 5/placebo TNM005 TNM005 on dose level 5 /placebo VARIZIG VariZIG VARIZIG 625 IU
- Primary Outcome Measures
Name Time Method Number of participants Physical examinations abnormalities Up to 120 days post dosing Physical examination includes assessments of general appearance, skin, lymph nodes, head.neck, lung, heart, abdomen, spine, extremities, nervous system, etc.
Incidence of AEs Up to 120 days post dosing Number of participants with abnormalities of 12-lead electrocardiogram (ECG) parameters Up to 120 days post dosing ECG parameters include heart rate, PR interval, RR interval, ORS duration, QTcF interval.
Number of participants with abnormalities of clinical laboratory tests Up to 120 days post dosing Clinical laboratory tests include hematology, biochemistry, coagulation, and urinalysis.
Number of participants with abnormalities of vital signs Up to 120 days post dosing Vital signs measured include blood pressure, pulse rate, temperature, and respiration rate.
- Secondary Outcome Measures
Name Time Method AUC0-∞ Up to 120 days post dosing Area under the plasma concentration-time curve from time 0 (predose) extrapolated to infinite time.
CL/F Up to 120days post dosing Apparent clearance
AUC0-t Up to 120 days post dosing Area under the plasma concentration-time curve from time 0 (predose) to the last time point with a detectable plasma concentration (Tlast.).
t1/2 of anti-varicella-zoster virus (VZV) antibody level (both baseline corrected and uncorrected) Up to 120days post dosing Elimination half-life of antibody level of anti-VZV
Cmax Up to 120days post dosing Maximum plasma concentration
Tmax Up to 120 days post dosing Time to reach maximum plasma concentration
Vd/F Up to 120days post dosing Apparent volume of distribution
ADA Up to 120days post dosing Incidence of anti-drug antibody (ADA) to TNM005 in serum
t1/2 Up to 120days post dosing Elimination half-life
λz Up to 120days post dosing Terminal disposition rate constant
Trial Locations
- Locations (1)
ICON, plc
🇺🇸Salt Lake City, Utah, United States