Clinical Trials Directory

Trials / Completed

CompletedNCT02956421

Efficacy and Safety of a PIKA Rabies Vaccine Containing the PIKA Adjuvant With an Accelerated Regimen

Phase II Study to Determine the Efficacy and Safety of PIKA Rabies Vaccine Containing the PIKA Adjuvant With an Accelerated Regimen

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
126 (actual)
Sponsor
Yisheng Biopharma (Singapore) Pte. Ltd. · Industry
Sex
All
Age
21 Years – 65 Years
Healthy volunteers
Accepted

Summary

Phase II clinical study for an investigational PIKA(Polyinosinic Polycytidylic Acid Based Adjuvant) rabies vaccine comprising Inactivated and Purified Rabies Virus (IPRV) and the PIKA adjuvant. The primary objective of the study is to evaluate the efficacy and safety profile of the vaccine composition in healthy adult volunteers under the accelerated regimen. The secondary objective is to achieve higher seroconversion of the vaccine under accelerated regimen at Day 7.

Detailed description

A multi-center, open labelled, randomized study in healthy naïve adult subjects. Subjects were randomly assigned to groups A (60) and B (60). Group A as a control arm of the study, had received a commercially available rabies vaccine, RABIPUR®. Group B had received doses of the investigational PIKA rabies vaccine in an accelerated regimen. Group A followed the vaccine regimen of (1-1-1-1),one injection on days 0, 3, 7 and 14 was administered respectively. Group B received the accelerated regimen (2-2-1), two injections on both days 0 and 3 were administered in different arms; and only one injection was administered on day 7. Each vaccine dose comprise 1.0 ml of PIKA rabies vaccine for Group B and 1.0 ml of RABIPUR® for Group A after reconstitution. The route of administration is intramuscular injection, given in the deltoid region of the arm.

Conditions

Interventions

TypeNameDescription
BIOLOGICALRABIPUR®Biological rabies vaccine
BIOLOGICALPIKA rabies vaccineBiological rabies vaccine

Timeline

Start date
2016-02-01
Primary completion
2016-10-01
Completion
2016-10-01
First posted
2016-11-07
Last updated
2016-11-08

Locations

2 sites across 1 country: Singapore

Source: ClinicalTrials.gov record NCT02956421. Inclusion in this directory is not an endorsement.