Transgene announces promising Phase I preliminary results of its HCV therapeutic vaccine
Preliminary analysis demonstrates a favourable safety profile and shows antiviral activity of TG4040 on chronically infected treatment-naïve patients
Preliminary analysis performed on the 15 patients after the three weekly injections, but prior to receiving the boost injection, shows that TG4040 has a favourable safety profile across all doses. The most common side effects are mild to moderate injection site reactions. On April 30th, 2008 the Independent Safety Committee stated that it had no safety concerns and indicated that it is appropriate to continue the study. Furthermore, six out of the 15 patients experienced a viral load reduction ranging from 0.5 to 1.4 log10, clearly indicating an effect of the vaccine on viral replication.
"These results, despite their preliminary and partial nature, are very encouraging and indicate that TG4040 is active against hepatitis C", said Philippe Archinard, Chief Executive Officer of Transgene. "These initial Phase I results clearly support pursuing and intensifying the clinical development of this novel therapeutic approach. We expect to present more detailed data, including boost vaccination results, by the fourth quarter of 2008."
Transgene's TG4040 product is based on the MVA virus carrying and expressing non-structural proteins (NS3, NS4 and NS5B) of the hepatitis C virus. The MVA vector is a highly attenuated strain of vaccinia virus that combines an extensive history of safety with the ability to stimulate a strong immune response to antigens.
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