|
Flu
|
Adjuvant formulation to increase dosage; Development of proteomic biomarker |
Process engineering and early testing |
|
HSV-2 (Herpes Simplex Virus type 2) |
Adenovirus; DNA |
Process engineering and early testing |
|
Hepatitis C |
Novel compounds |
Antigen discovery |
|
Hepatitis C |
NK and T cells |
Antigen discovery |
|
Syphilis |
|
Process engineering and early testing |
|
E. coli O157 |
for cattle |
Process engineering and early testing |
|
HIV (Human Immunodeficiency Virus) |
Novel candidates |
Process engineering and early testing |
|
Malaria |
Human challenge (pre-erythrocytic antigen) |
Process engineering and early testing |
|
Malaria |
Pregnancy |
Process engineering and early testing |
|
Malaria |
Genetically attenuated parasites |
Process engineering and early testing |
|
Hepatitis B |
|
Formulation/stabilization |
|
DTP-HepB-Hib (Diptheria-HepatitisB-Haemophilus Influenzae Type b) |
|
Formulation/stabilization |
|
Rotavirus |
|
Process engineering / manufacturing & epidemiology |
|
Shigella |
|
Process engineering / manufacturing & epidemiology |
|
ETEC (Enterotoxigenic Escherichia coli) |
|
Process engineering / manufacturing & epidemiology |
|
Pneumococcus (Streptococcus pneumoniae) |
|
Process engineering / manufacturing & epidemiology |
Additional candidate immunogens within the WAVA members include Leishmania, Tuberculosis, Chlamydia, Salmonella, T pallidum, Delicobacter, Kaposi Sarcoma, Japanese Encephalitis, and Leprosy.
© Washington Vaccine Alliance