Tetanus
Conditions
Brief summary
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and Immunogenicity characteristics of GR2001 and compare the anti-tetanus neutralizing antibody titers of GR2001 with human tetanus immunoglobulin (HTIG)in healthy adult subjects.
Detailed description
This is a Multicentre, Randomized, Double-Blind, Placebo-Controlled, Phase I/II Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity of GR2001 Injection in Healthy Subjects. In the phase I part of the study, a total of 94 healthy subjects will be enrolled. The 94 healthy adult subjects will be enrolled into 7 cohorts sequentially. Each participant will receive a single IM dose of GR2001 or placebo or HTIG according to the cohort in which they were enrolled. After injection (Day 0), participants will remain in the study site for observation up to Day 1. The phase I part will last for 105 days following the assessments of safety, PK, PD and ADA. In the phase II part of the study, a total of 108 healthy subjects will be enrolled. The 108 healthy subjects will be randomly assigned to the experimental group and the control group based on a ratio of 1:1:1:2:2:2.The phase II part will last for 105 days following the assessments of safety, PK, PD and ADA.
Interventions
BIOLOGICALGR2001
intramuscular injection
BIOLOGICALPlacebo
intramuscular injection
BIOLOGICALHTIG
intramuscular injection
BIOLOGICALTetanus Toxoid
intramuscular injection
Sponsors
Genrix (Shanghai) Biopharmaceutical Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Masking description
Double Blind
Intervention model description
In the phase I part of the study, a total of 94 healthy subjects will be enrolled. The 94 healthy adult subjects will be enrolled into 7 cohorts sequentially. Each participant will receive a single IM dose of GR2001 or placebo or HTIG according to the cohort in which they were enrolled. After injection (Day 0), participants will remain in the study site for observation up to Day 1. The phase I part will last for 105 days following the assessments of safety, PK, PD and ADA. In the phase II part of the study, a total of 108 healthy subjects will be enrolled. The 108 healthy subjects will be randomly assigned to the experimental group and the control group based on a ratio of 1:1:1:2:2:2.The phase II part will last for 105 days following the assessments of safety, PK, PD and ADA.
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
1. Healthy male or female, 18-60 years of age (both inclusive); 2. Body mass index within 18.0-27.0 kg/m2 (both inclusive); 3. Subjects including partners are willing to voluntarily take effective contraceptive measures from screening to 6 months after the last study drug administration. 4. Completed written informed consent process, signed the informed consent forms and Agreed to complete all follow-ups.
Exclusion criteria
1. History or evidence of severe drug or excipient allergy; 2. History or evidence of tetanus infection; 3. Inoculation of tetanus vaccine within 10 years; 4. History or evidence of any other acute or chronic disease； 5. Known or suspected history of drug abuse； 6. Positive outcome for Tetanus-antibody IgG test; 7. Nursing mothers or pregnant women.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of AEs(Phase I) | Up to 105 days | Number of participants with treatment-related adverse events or serious adverse events. |
| Tetanus-antibody titer(Phase II) | 24 hours post administration | Tetanus-antibody titer post administration. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of AEs(Phase II) | Up to 105 days | Number of participants with treatment-related adverse events or serious adverse events. |
| Peak plasma concentration(Cmax) | Up to 105 days | Estimated by non-compartmental analysis (NCA) with WinNonlin. |
| Area under the plasma concentration versus time curve (AUC) | Up to 105 days | Estimated by non-compartmental analysis (NCA) with WinNonlin. |
| Time of maximum plasma concentration (Tmax) | Up to 105 days | Estimated by non-compartmental analysis (NCA) with WinNonlin. |
| Tetanus-antibody titer(Phase I/II) | Up to 105 days | Tetanus-antibody titer post administration. |
| Apparent total body clearance (CL/F) | Up to 105 days | Estimated by non-compartmental analysis (NCA) with WinNonlin. |
| Apparent volume of distribution (Vd/F) | Up to 105 days | Estimated by non-compartmental analysis (NCA) with WinNonlin. |
| The elimination rate constant (Kel) | Up to 105 days | Estimated by non-compartmental analysis (NCA) with WinNonlin. |
| Mean Residence Time (MRT) | Up to 105 days | Estimated by non-compartmental analysis (NCA) with WinNonlin. |
| Terminal half-life (T1/2) | Up to 105 days | Estimated by non-compartmental analysis (NCA) with WinNonlin. |
| Incidence of ADA(Phase I/II) | Up to 105 days | Incidence of ADA post administration. |
Countries
China
Outcome results
None listed