Immunogenicity and Safety Study of A New Chromatographically Purified Vero Cell Rabies Vaccine With ID Regimen and ERIG
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Purpose
A comparative,randomized (1:1)study to evaluate the safety and immunogenicity of a new chromatographically purified vero cell rabies vaccine (SPEEDA) and chromatographically purified vero cell rabies vaccine (SPEEDA)which is filled by Queen Saovabha Memorial Institute (TRCS SPEEDA)vs. reference vaccine (purified vero cell vaccine; VERORAB)when using with post-exposure rabies intradermal vaccination with or without equine rabies immunoglobulin.
| Condition | Intervention | Phase |
|---|---|---|
|
Rabies Vaccine |
Biological: SPEEDA and TRCS SPEEDA |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Factorial Assignment Masking: Single Blind (Subject) Primary Purpose: Treatment |
| Official Title: | An Immunogenicity and Safety Study of Modified TRC-ID Regimen With A New Chromatographically Purified Vero Cell Rabies Vaccine(SPEEDA/TRCS SPEEDA) and Rabies Immunoglobulin |
- immunogenicity (the level of rabies neutralizing antibodies by RFFIT test) [ Time Frame: 32 months ] [ Designated as safety issue: Yes ]The immunogenicity (Rabies neutralizing antibodies) would be checked from the blood samples for 7 times (on days 0,7,14,28,90,180 and 360)for one year duration in each phase.
- safety [ Time Frame: 32 months ] [ Designated as safety issue: Yes ]This would based on general examination, local examination and subjective evaluation of both solicited and unsolicited adverse events.
| Estimated Enrollment: | 210 |
| Study Start Date: | June 2010 |
| Estimated Study Completion Date: | February 2013 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: SPEEDA with modified TRC-ID regimen
35 healthy volunteers
|
Biological: SPEEDA and TRCS SPEEDA
For modified TRC-ID regimen,0.1 ml of SPEEDA, TRCS SPEEDA or VERORAB will be given at each of two sites,intradermally on upper arms on days 0,3,7 and 28. For ESSEN regimen, 1 vial of SPEEDA will be given intramuscularly at upper arm on days 0,3,7,14 and 28. For ERIG,it would be given in a single dose 40 IU/Kg at the same time as the first dose of vaccine. ERIG will be infiltrated around and into all wounds as recommended by WHO for patients in group IV and injected intramuscular at each of both gluteal areas for participants in group III,V,VI Other Names:
|
|
Active Comparator: VERORAB with modified TRC-ID regimen
35 healthy volunteers
|
Biological: SPEEDA and TRCS SPEEDA
For modified TRC-ID regimen,0.1 ml of SPEEDA, TRCS SPEEDA or VERORAB will be given at each of two sites,intradermally on upper arms on days 0,3,7 and 28. For ESSEN regimen, 1 vial of SPEEDA will be given intramuscularly at upper arm on days 0,3,7,14 and 28. For ERIG,it would be given in a single dose 40 IU/Kg at the same time as the first dose of vaccine. ERIG will be infiltrated around and into all wounds as recommended by WHO for patients in group IV and injected intramuscular at each of both gluteal areas for participants in group III,V,VI Other Names:
|
|
Active Comparator: SPEEDA with modified TRC-ID regimen plus ERIG
35 healthy volunteers
|
Biological: SPEEDA and TRCS SPEEDA
For modified TRC-ID regimen,0.1 ml of SPEEDA, TRCS SPEEDA or VERORAB will be given at each of two sites,intradermally on upper arms on days 0,3,7 and 28. For ESSEN regimen, 1 vial of SPEEDA will be given intramuscularly at upper arm on days 0,3,7,14 and 28. For ERIG,it would be given in a single dose 40 IU/Kg at the same time as the first dose of vaccine. ERIG will be infiltrated around and into all wounds as recommended by WHO for patients in group IV and injected intramuscular at each of both gluteal areas for participants in group III,V,VI Other Names:
|
|
Active Comparator: VERORAB with modified TRC-ID regimen plus ERIG
35 WHO category III patients
|
Biological: SPEEDA and TRCS SPEEDA
For modified TRC-ID regimen,0.1 ml of SPEEDA, TRCS SPEEDA or VERORAB will be given at each of two sites,intradermally on upper arms on days 0,3,7 and 28. For ESSEN regimen, 1 vial of SPEEDA will be given intramuscularly at upper arm on days 0,3,7,14 and 28. For ERIG,it would be given in a single dose 40 IU/Kg at the same time as the first dose of vaccine. ERIG will be infiltrated around and into all wounds as recommended by WHO for patients in group IV and injected intramuscular at each of both gluteal areas for participants in group III,V,VI Other Names:
|
|
Active Comparator: SPEEDA with ESSEN IM regimen plus ERIG
35 healthy volunteers
|
Biological: SPEEDA and TRCS SPEEDA
For modified TRC-ID regimen,0.1 ml of SPEEDA, TRCS SPEEDA or VERORAB will be given at each of two sites,intradermally on upper arms on days 0,3,7 and 28. For ESSEN regimen, 1 vial of SPEEDA will be given intramuscularly at upper arm on days 0,3,7,14 and 28. For ERIG,it would be given in a single dose 40 IU/Kg at the same time as the first dose of vaccine. ERIG will be infiltrated around and into all wounds as recommended by WHO for patients in group IV and injected intramuscular at each of both gluteal areas for participants in group III,V,VI Other Names:
|
|
Active Comparator: TRCS SPEEDA with modified TRC-ID regimen plus ERIG
35 healthy volunteers
|
Biological: SPEEDA and TRCS SPEEDA
For modified TRC-ID regimen,0.1 ml of SPEEDA, TRCS SPEEDA or VERORAB will be given at each of two sites,intradermally on upper arms on days 0,3,7 and 28. For ESSEN regimen, 1 vial of SPEEDA will be given intramuscularly at upper arm on days 0,3,7,14 and 28. For ERIG,it would be given in a single dose 40 IU/Kg at the same time as the first dose of vaccine. ERIG will be infiltrated around and into all wounds as recommended by WHO for patients in group IV and injected intramuscular at each of both gluteal areas for participants in group III,V,VI Other Names:
|
Detailed Description:
Rabies is an important world health problem especially in developing countries.Although the case-fatality ratio of human rabies is 100%,the disease is preventable by the modern cell-culture vaccine and rabies immunoglobulin.Post-exposure rabies vaccination with the modified Thai Red Cross intradermal(modified TRC-ID)regimen has been approved by WHO and proven to be immunogenic and effective. It represents a significant saving in vaccine cost and is now established in several developing countries. SPEEDA,chromatography purified vero cell derived rabies vaccine,approved by Thai FDA on 8 April 2009 and drug registration code of SPEEDA is 1C 90022/51. This study has a goal to determine the immunogenicity and safety of SPEEDA and TRCS-SPEEDA (SPEEDA which is filled by Queen Saovabha Memorial Institute)vs. reference vaccine (purified vero cell vaccine; VERORAB)when using with post-exposure rabies intradermal vaccination with or without equine rabies immunoglobulin.
Eligibility| Ages Eligible for Study: | 15 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- subjects are healthy population older than 15 years.
- subjects are willing to give signed informed consents.
- subjects are willing to give blood samples on recommended days.
- subjects are available for follow up according to the table of administration
Exclusion Criteria:
- subjects who had received any type of rabies vaccination in the past
- subjects who had received rabies immunoglobulin in the past
- subjects who had known as immunocompromised hosts
- subjects on steroids or any other immunosuppressant
- subjects on concomitant antimalarials
- subjects who have received of any blood products within the previous 3 months
- subjects with history of allergy to any ingredient of the vaccine
- subjects who had known as pregnancy in first recruitment
Contacts and Locations| Contact: Suda Sibunruang, M.D. | +66 1 7366076 | sudapunrin@gmail.com |
| Contact: Terapong Tantawichien, M.D., Prof. | +66 1 7350654 | terapong_tantawichien@hotmail.com |
| Thailand | |
| Queen Saovabha Memorial Institute | Not yet recruiting |
| Bangkok, Thailand, 10330 | |
| Contact: Suda Sibunruang, MD. +66 1 7366076 sudapunrin@gmail.com | |
| Contact: Thanphet Tantawichien, RN +66 1 9074652 qsmithanphet@yahoo.com | |
| Principal Investigator: Terapong Tantawichien, MD. Prof. | |
| Suda Sibunruang | Recruiting |
| Bangkok, Thailand, 10130 | |
| Contact: Suda Sibunruang, MD +66 2 252 0161 ext 125 sudapunrin@gmail.com | |
| Principal Investigator: Suda Sibunruang, MD | |
| Principal Investigator: | Terapong Tantawichien, MD.,Prof | Queen Saovabha Memorial Institute |
More Information
No publications provided
| Responsible Party: | Suda Sibunruang, Principal investigator, Queen Saovabha Memorial Institute |
| ClinicalTrials.gov Identifier: | NCT01137045 History of Changes |
| Other Study ID Numbers: | RC5301 |
| Study First Received: | June 3, 2010 |
| Last Updated: | May 30, 2012 |
| Health Authority: | Thailand: Ethical Committee |
Keywords provided by Queen Saovabha Memorial Institute:
|
rabies vaccine vero cells serology safety |
Additional relevant MeSH terms:
|
Rabies Rhabdoviridae Infections Mononegavirales Infections RNA Virus Infections Virus Diseases |
ClinicalTrials.gov processed this record on May 19, 2013