ID | 1173 |
Name of the vaccine | VLA15 |
Microbe | Bacteria |
Disease name | Lyme disease (Lyme borreliosis) |
Name of bacteria | Borrelia burgdorferi |
Type of vaccine | Recombinant |
Nucleic acid content | DNA |
Age | 5 to 65 years |
Description of the vaccine | Multivalent recombinant OspA (Outer Surface Protein A) based vaccine. |
Name of the manufacturer | Valneva Austria GmbH and Pfizer |
Name of the manufacturing country | United States |
Year of manufacture | 2026 |
Clinical Phase status | Clinical - Phase 2 |
Bacterial strain | Gram-negative spirochete bacteria. |
Efficacy | NA |
Vaccine formulation | NA |
Dosage | Three (month 0-2-6) or two (month 0-6) vaccinations. |
Mechanism of action | Targets the outer surface protein A (OspA) of the bacteria. |
Route of administration | Intramuscular |
Indications | Protects from six serotypes of Borrelia. |
Export | NA |
Approval | NA |
Adjuvant | Alum |
Repurposing | NA |
Side effects of vaccine | NA |
Post vaccination | NA |
Dose type | Combination doses |
Interspecies transfer | Yes (from the bite of infected blacklegged ticks) |
PubMed identifier | NA |
Clinical trial number | NCT04801420 |
Reference | https://www.clinicaltrialsarena.com/news/pfizer-valneva-lyme-disease/ |
Other name | NA |
Additional Links | NA
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