Immunity Duration of Rabies Vaccine and Booster Dose Effects at 10 Years Post-primary Vaccination
NCT03774628 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 342
Last updated 2020-12-01
Summary
A rabies vaccine (human diploid cell) for human use, Freeze-dried produced by Chengdu Kanghua Biological Products Co.,Ltd is used to prevent human rabies. The vaccine was completed in the Phase III clinical trial from August 2008 to February 2009 in Lianshui County, Jiangsu Province (Approval of Drug Clinical Trial No. 2008L03156). A total of 1200 subjects aged 10-60 years were randomly assigned trial group (Kanghua vaccine group, 600 participants) and control groups (Pasteur vaccine group, 600 participants). The result showed that this vaccine could provide good immunogenicity and mild adverse reactions. On April 28, 2012, the drug registration approval was obtained (Approval No. 2012S00222).
To disclose the effects of booster immunization of human diploid cell rabies vaccine (HDCV) after eight years of primary vaccination. Sixty subjects who had participated the phase Ⅲ clinical trial of freeze-dried HDCV were selected and given booster immunization after eight years of primary vaccination. The result showed that the freeze-dried HDCV has good immune effects with one-dose of booster immunization after eight years of primary vaccination. In order to find a ten years of immunization persistence and booster dose immune effect, the investigators decided to perform this immunization persistence and booster immunity trial among these subjects who had received five doses of rabies vaccine vaccines (around ten years after the fundamental immunity). The investigators do the recruitment among these subjects who had participated in the previous phase Ⅲ trail and the subjects were divided into two layers, such as trial group (Kanghua vaccine group) and the control group (Paste vaccine group). Each layer of the subjects randomly received one booster dose (Day 0) and two booster doses (Day 0, 3) the freeze-dried HDCV in a ratio of 1:1.
Conditions
- Rabies
Interventions
- BIOLOGICAL
-
Chengdu Kanghua (one booster shot)
A rabies vaccine (human diploid cell) for human use, Freeze-dried produced by Chengdu Kanghua Biological Products Co.,Ltd. 1.0 ml experimental vaccine on day 0
- BIOLOGICAL
-
Chengdu Kanghua (two booster shots)
A rabies vaccine (human diploid cell) for human use, Freeze-dried produced by Chengdu Kanghua Biological Products Co.,Ltd. 1.0 ml experimental vaccine on day 0 and 3
Sponsors & Collaborators
-
Jiangsu Province Centers for Disease Control and Prevention
lead NETWORK
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 20 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2018-08-01
- Primary Completion
- 2019-02-19
- Completion
- 2019-02-19
Countries
- China
Study Locations
More Related Trials
-
To Evaluate the Immunogenicity and Safety of Two Different Immunization Schedules of Rabies Vaccine (Vero Cell)
NCT06177249 ·Status: COMPLETED ·Phase: PHASE3
-
Prevention of Rabies With Four Doses of Rabies Vaccine
NCT05545371 ·Status: ENROLLING_BY_INVITATION ·Phase: PHASE3
-
A Clinical Trial of Freeze-dried Human Rabies Vaccine (MRC-5 Cells)
NCT06078423 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Immunogenicity of Freeze-dried Rabies Vaccine(MRC-5 Cell) in Chinese Humans
NCT02288286 ·Status: COMPLETED ·Phase: PHASE3
-
A Clinical Trial of Freeze-dried Human Rabies Vaccine (Vero Cells)
NCT04852068 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
The Safety Research of Freeze-dried Rabies Vaccine(MRC-5 Cell) in Chinese Humans
NCT02281396 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate Persistence of Immune Responses After Post-exposure Prophylaxis of Rabipur® (Purified Chicken-embryo Cell Rabies Vaccine) in Chinese Children
NCT02991872 ·Status: COMPLETED ·Phase: PHASE4
-
A Clinical Trial of Rabies Vaccine(Human Diploid Cell)for Human Use,Freeze-dried
NCT07021703 ·Status: RECRUITING ·Phase: PHASE1
-
A Phase 3 Clinical Trial to Evaluate Long-term Immunogenicity and Boostability of Purified Chick-Embryo Cell Rabies Vaccine in Adults Following Primary Series of Pre/Exposure Prophylaxis.
NCT02545517 ·Status: COMPLETED ·Phase: PHASE3
-
Purified Rabies Vaccine for Human Use (Chick-embryo Cell)
NCT00345319 ·Status: COMPLETED ·Phase: PHASE3
-
A Clinical Trial of Rabies Vaccine(Human Diploid Cell)for Human Use,Freeze-dried in a Population Aged 10 to 60 Years
NCT07275645 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Phase 3 Clinical Trial for a Rabies Vaccine (Vero Cell) for Human Use in Healthy Chinese Subjects
NCT02491541 ·Status: COMPLETED ·Phase: PHASE3
-
Clinical Trial of Freeze-dried Human Rabies Vaccine (Without Serum Vero Cells)
NCT05969626 ·Status: UNKNOWN ·Phase: PHASE3
-
Safety, Pharmacokinetics, and Pharmacodynamic Testing of Rabies mAb CBB 1
NCT05832073 ·Status: UNKNOWN ·Phase: EARLY_PHASE1
-
Rabies mAb CBB 1 Combination Vaccine in Healthy People With Antibody Neutralization Activity and Safety Phase Clinical Trials
NCT06548139 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
Safety and Immunogenicity of Two Intradermal Rabies Vaccine Regimens Administered With and Without Human Rabies Immunoglobulin in Subjects ≥ 1 Years of Age
NCT02177032 ·Status: COMPLETED ·Phase: PHASE3
-
Persistence of Rabies Antibody 1-5 Years After the Post-exposure Prophylaxis With Vero Cell Antirabies Vaccine and Antibody Response to a Single Booster Dose
NCT01173302 ·Status: UNKNOWN ·Phase: PHASE4
-
Observation on the Immune Persistence of People Aged 10-60 Years Old Immunized With Five Doses of Rabies Vaccine
NCT05547815 ·Status: COMPLETED ·Phase: PHASE4
-
Safety Study of Rabies Vaccine INDIRAB® Five Doses (0.5ml) Post Exposure Administered Intramuscularly
NCT02729168 ·Status: COMPLETED ·Phase: NA
-
Immunogenicity of Rabies Vaccine for Pre Exposure Prophylaxis
NCT02374814 ·Status: COMPLETED ·Phase: PHASE4
-
A Comparison of Safety and Immunogenicity of Rabies Pre Exposure Prophylaxis Regimen Between Gvt of India Approved and WHO Approved.
NCT06066294 ·Status: RECRUITING ·Phase: PHASE3
-
A Study to Evaluate the One Year Long-term Persistence of Immune Responses Following Two Different Rabies Vaccine Post-exposure Regimens in Chinese Children
NCT03192371 ·Status: WITHDRAWN ·Phase: PHASE4
-
Single Center, Open Label, Follow up Study in Subjects Who Previously Received Rabies Vaccine as Simulated Post-Exposure Regimen
NCT01067079 ·Status: TERMINATED
-
Immunogenicity and Safety of Rabies Vaccine (Serum-free Vero Cell) in a Pre-exposure Prophylaxis Regimen
NCT07055295 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Clinical Study on Immunogenicity and Safety of Lyophilized Vero Cell-Derived Human Rabies Vaccine in Special Populations
NCT07120464 ·Status: RECRUITING