Drug intelligence / Profile preview

ChAd63 PvDBP + MVA PvDBP

Development stage
Phase 2
Lead developer
University of Oxford
Modality
Viral Vector Vaccines → Recombinant Vaccines → Prophylactic Vaccines → Vaccines & Immunotherapeutics, DNA Vaccines → Plasmid DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Viral Vectors → Gene Addition/Replacement → Gene Therapies
Administration
Intramuscular
01

Overview

ChAd63 PvDBP + MVA PvDBP is a heterologous prime-boost malaria vaccine candidate targeting *Plasmodium vivax*. The regimen uses two recombinant viral vectors to deliver the gene encoding region II of the Duffy-binding protein (PvDBPII) from *Plasmodium vivax*: chimpanzee adenovirus 63 (ChAd63) as the priming vector and modified vaccinia virus Ankara (MVA) as the booster. Both vectors are genetically engineered to express the same malaria antigen. The vaccines are administered sequentially—ChAd63 PvDBP first, followed by MVA PvDBP approximately 8 weeks later. The goal is to induce both antibody and cellular immune responses against the blood-stage of *Plasmodium vivax* by generating immunity to a key protein required for parasite invasion of human red blood cells. Developed primarily for prevention of vivax malaria in healthy adults, this combination has been evaluated in Phase I/IIa clinical trials but did not demonstrate sufficient efficacy in reducing parasite growth or delaying symptoms compared with controls[1][3][4][5][6]. Both components were well tolerated with mainly mild and short-lived side effects.

Other names
ChAd63/MVA PvDBPVV-PvDBPII
02

Targets

PvDBP-II (Plasmodium vivax Duffy binding protein region II)

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