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A series of phase I clinical studies were conducted to evaluate the safety of plasmid DNA and modified vaccinia virus Ankara malaria vaccines. The vaccines each encoded a polyepitope string fused to whole Plasmodium falciparum TRAP antigen. Forty-three healthy adult volunteers received the vaccines alone or in DNA/MVA prime-boost combinations. The DNA vaccine was administered either intramuscularly by needle or intradermally by a needleless delivery device. The MVA vaccine was administered intradermally by needle. The vaccines were well-tolerated by all three routes and in various DNA/MVA immunisation regimes. There were no severe or serious adverse events. © 2002 Elsevier Science Ltd. All rights reserved.

Original publication

DOI

10.1016/S0264-410X(02)00771-5

Type

Journal article

Journal

Vaccine

Publication Date

16/05/2003

Volume

21

Pages

1995 - 2002