<p>Group A1, participants receiving PCECV according to the 4-site/1-week ID regimen; Group A2, participants receiving PCECV according to the 4-site/1-week ID regimen and HRIG at first visit; Group B1, participants receiving PCECV according to the 2-site/TRC ID regimen; Group B2, participants receiving PCECV according to the 2-site/TRC ID regimen and HRIG at first visit; PCECV, purified chick embryo cell culture vaccine; ID, intradermal; HRIG, human rabies immunoglobulin; TRC, Thai Red Cross; D, day; BD, blood draw. Administration schemes represent injection sites. The syringe symbolizes 1 injection of 0.1 mL of PCECV vaccine.</p
<p><b>Introduction</b>: Fifteen million people each year receive post-exposure prophylaxis (PEP) to ...
AbstractObjective: To determine the efficacy of a cost-effective multi-site intradermal regimen with...
<p>The CONSORT diagram indicates the number of subjects screened to complete enrollment of 31 subjec...
<p>Group A1, participants receiving PCECV according to the 4-site/1-week ID regimen; Group A2, parti...
AbstractObjectives: Currently, two intradermal regimens for the administration of cell culture rabie...
The standard six-dose intramuscular (i.m.) rabies post-exposure vaccine regimen using a new purified...
AbstractObjectives: Currently, two intradermal regimens for the administration of cell culture rabie...
Background: In Australia, recommendations for pre-exposure rabies vaccination involve 3 doses of vac...
This phase III clinical trial compared the immunogenicity and safety of a purified chick-embryo cell...
PURPOSE: To test the immunogenicity of the WHO recommended "2-2-2-0-1-1" post-exposure rabies vacc...
PURPOSE: To test the immunogenicity of the WHO recommended "2-2-2-0-1-1" post-exposure rabies vacc...
<p>The CONSORT diagram indicates the number of subjects screened to complete enrollment of 40 subjec...
© 2018 Kerdpanich et al. http://creativecommons.org/licenses/by/4.0/ Background: This phase III clin...
Objective: Our research was aimed at the determination of seroconversion following the vaccination o...
<div><p>Background</p><p>This phase III clinical trial compared the immunogenicity and safety of a p...
<p><b>Introduction</b>: Fifteen million people each year receive post-exposure prophylaxis (PEP) to ...
AbstractObjective: To determine the efficacy of a cost-effective multi-site intradermal regimen with...
<p>The CONSORT diagram indicates the number of subjects screened to complete enrollment of 31 subjec...
<p>Group A1, participants receiving PCECV according to the 4-site/1-week ID regimen; Group A2, parti...
AbstractObjectives: Currently, two intradermal regimens for the administration of cell culture rabie...
The standard six-dose intramuscular (i.m.) rabies post-exposure vaccine regimen using a new purified...
AbstractObjectives: Currently, two intradermal regimens for the administration of cell culture rabie...
Background: In Australia, recommendations for pre-exposure rabies vaccination involve 3 doses of vac...
This phase III clinical trial compared the immunogenicity and safety of a purified chick-embryo cell...
PURPOSE: To test the immunogenicity of the WHO recommended "2-2-2-0-1-1" post-exposure rabies vacc...
PURPOSE: To test the immunogenicity of the WHO recommended "2-2-2-0-1-1" post-exposure rabies vacc...
<p>The CONSORT diagram indicates the number of subjects screened to complete enrollment of 40 subjec...
© 2018 Kerdpanich et al. http://creativecommons.org/licenses/by/4.0/ Background: This phase III clin...
Objective: Our research was aimed at the determination of seroconversion following the vaccination o...
<div><p>Background</p><p>This phase III clinical trial compared the immunogenicity and safety of a p...
<p><b>Introduction</b>: Fifteen million people each year receive post-exposure prophylaxis (PEP) to ...
AbstractObjective: To determine the efficacy of a cost-effective multi-site intradermal regimen with...
<p>The CONSORT diagram indicates the number of subjects screened to complete enrollment of 31 subjec...