CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 16 enrolled
Drug / intervention
ChAd63 PvDBP and MVA PvDBPbiological
Likely dose
Not stated in 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/NCT04009096
NCT04009096Phase 2Completed

A Phase IIa Challenge Study to Assess Efficacy of the Plasmodium Vivax Malaria Vaccine Candidates ChAd63 PvDBP and MVA PvDBP in Healthy Adults Living in the UK

University of Oxford·interventional·Posted Jul 5, 2019·Updated Apr 12, 2024

In Brief

A Phase 2 clinical trial evaluating ChAd63 PvDBP and MVA PvDBP for Malaria, Vivax. Completed, enrolled 16 participants across 1 site.

Detailed Summary

This is an open label, Phase IIa, controlled human malaria infection (CHMI) study aimed to assess whether the new vivax malaria vaccines ChAd63 PvDBP and MVA PvDBP can protect against malaria infection. The participants will receive one or two doses of ChAd63 PvDBP followed by one dose of MVA PvDBP 8 weeks later. Approximately 4 weeks after the second vacccination, the volunteers will be challenged (deliberately infected) with malaria by intravenous injection blood-stage

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMalaria, Vivax
CountriesUnited Kingdom
Collaborators--

Timeline

Phase 2CompletedFinished
2020202120222023202420252026
First PostedJul 5, 2019
Enrollment StartJul 18, 2019
Primary CompletionJul 7, 2022
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 7.0 years ago

Interventions

ChAd63 PvDBP and MVA PvDBPbiological

one dose of 5 x 10\^10 vp ChAd63 PvDBP and one dose of 2 x 10\^8 pfu MVA PvDBP 8 weeks later, in a heterologous prime-boost regimen.