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. 2014 Dec 6;2(1):72–82. doi: 10.1007/s40521-014-0038-5

Table 1.

Clinical trials using virus-like particles (VLPs) and CG motifs (CpGs) [41]

Vaccine Treatment arms Patients and disease Study design Reference
Qβ VLP coupled to Der p 1-derived peptide (Qβ-Der p 1). Note that this VLP was loaded with E. coli RNA

i.m. 50 μg Qβ-Der p 1 (n = 6),

s.c. 50 μg Qβ-Der p 1 (n = 6),

i.m. 10 μg Qβ-Der p 1 (n = 6),

s.c. 10 μg Qβ-Der p 1 (n = 6)

24 volunteers; healthy Randomized, monocentric, open-label [39•]
Amb a 1 conjugated to type B CpG-ODN Verum (n = 14), placebo (n = 11) 25 patients; allergic to ragweed; rhinitis Randomized, double-blind, placebo-controlled [38••]
Qβ VLP filled with type A CpG-ODN (QbG10) + HDM extract QbG10 + HDM allergen (n = 20) 20 patients; allergic to HDM; rhinoconjunctivitis Randomized, monocentric, open-label [71]
Qβ VLP filled with type A CpG-ODN (QbG10) 0.5 mg QbG10 (n = 99), 1 mg QbG10 (n = 103), placebo (n = 97) 299 patients; allergic to HDM; rhinoconjunctivitis Randomized, double-blind, placebo-controlled [42••]

HDM house dust mite, i.m. intramuscular, ODN oligodeoxynucleotide, s.c. subcutaneous