CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 87 enrolled
Drug / intervention
Inactivated Poliomyelitis Vaccine (IPV) +2 morebiological
Likely dose
Inactivated Poliomyelitis Vaccine (IPV) 0.5 mLfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04232943
NCT04232943Phase 1Completed

A Phase 1 Randomized Study to Examine the Safety, Tolerability, and Immunogenicity of Inactivated Poliovirus Vaccine (IPV) With or Without E.Coli Double Mutant Heat Labile Toxin (dmLT) and Impact on Poliovirus Shedding Post-bOPV Challenge in Healthy IPV-Primed Adult Subjects

PATH·interventional·Posted Jan 18, 2020·Updated Sep 6, 2022

In Brief

A Phase 1 clinical trial evaluating Inactivated Poliomyelitis Vaccine (IPV), E.coli Double Mutant Heat-Labile Toxin (dmLT) (adjuvant), and 1 other intervention for Polio. Completed, enrolled 87 participants across 1 site.

Detailed Summary

In this study, the safety and tolerability of inactivated polio vaccine (IPV) co-administered with dmLT will be assessed, as well as whether co-administration of dmLT with IPV enhances mucosal responses compared to those with IPV alone.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPolio
CountriesBelgium
Collaborators--

Timeline

Phase 1CompletedFinished
2020202120222023202420252026
First PostedJan 18, 2020
Enrollment StartJan 22, 2020
Primary CompletionFeb 1, 2021
TodayJul 2, 2026
Enrollment to primary: 1.0 yearsPosted 6.5 years ago

Interventions

Inactivated Poliomyelitis Vaccine (IPV)biological

IMOVAX® Polio is a highly purified, inactivated poliovirus vaccine. Each 0.5 mL dose contains: * Type 1 (Mahoney) 40 D-antigen units * Type 2 (MEF1) 8 D-antigen units * Type 3 (Saukett) 32 D-antigen units

E.coli Double Mutant Heat-Labile Toxin (dmLT) (adjuvant)biological

LT (R192G/L211A), or "dmLT," is a protein toxoid derived from wild-type enterotoxigenic Escherichia coli (ETEC) labile toxin (LT). The LT toxin has been shown to have inherent mucosal adjuvant properties for co-administered antigens and thus has potential as a mucosal adjuvant for different co-administered vaccines. LT has been genetically modified by replacing the arginine at amino acid position 192 with glycine and the leucine at amino acid position 211 with alanine. These two amino acid substitutions take place in proteolytic cleavage sites, which are critical for activation of the secreted toxin molecules.

Bivalent Oral Polio Vaccine (bOPV)biological

Polio Sabin™ One and Three (oral) is a bivalent, live attenuated poliomyelitis virus vaccine of the Sabin strains Type 1 (LSc, 2ab) and Type 3 (Leon 12a, 1b), propagated in MRC5 human diploid cells. Each dose (0.1 mL) contains not less than 10⁶ 50% cell culture infectious dose (CCID₅₀) of Type 1 and 10⁵·⁸ CCID₅₀ of Type 3.