Table 1.
Vaccine Class | Vaccine Name | Manufacturer or sponsor |
Most Advanced Clinical Trial Status* |
Pros | Cons | Comments |
---|---|---|---|---|---|---|
Vectored, Live |
rVSV-ZEBOV [12– 14,17–19,21,22] |
Merck Sharp & Dohme Corp, NewLink Genetics, Public Health Agency of Canada |
Phase 3 | Single vaccination is highly immunogenic |
Some safety concerns |
|
HPIV3-EbovZ GP [30–32] |
NIAID | Phase 1 | Intranasal administration may elicit more robust mucosal immunity |
Pre-existing immunity to vector |
||
Vectored, non- replicating |
ChAd3.EBOZ / ChAd3.EBO [52– 57] |
Glaxo Smith Kline, NIAID | Phase 2 | Safety | Requires boost vaccination |
|
Ad26.ZEBOV [40,63] |
Crucell Holland BV (Johnson & Johnson) |
Phase 3 | Safety | Requires boost vaccination |
Phase 4 retrospective evaluation underway though product is not licensed (NCT02661464) |
|
Ad5-EBOV [65,66] | Tianjin CanSino Biotechnology and Beijing Institute of Biotechnology |
Phase 2 | Pre-existing immunity to Ad5 vector |
Requires boost vaccination |
||
VRC- EBOADV018-00- VP [38,39] |
NIAID | Phase 1 | Pre-existing immunity to Ad5 vector |
Requires boost vaccination |
No longer active | |
MVA-BN-Filo [54] | Bavarian Nordic GmbH / Crucell Holland BV (Johnson & Johnson) |
Phase 3 | Safety | Immunogenicity; Requires heterotypic pairing for vaccine administration |
Phase 4 retrospective evaluation underway though product is not licensed (NCT02661464) |
|
MVA-EbolaZ (VRC- EBOMVA079-00- VP)[52] |
NIAID | Phase 1 | Safety | Immunogenicity; Requires heterotypic pairing for vaccine administration |
||
DNA | VRC- EBODNA023-00- VP, VRCEBODNA012- 00-VP, and VRCMARDNA025- 00-VP [49,77–79] |
NIAID | Phase 1 | Safety, flexible platform, low cost |
Effective administration requires electroporation technology; requires boost vaccination for immunogenicity |
No longer active |
INO-4201, -4202, and -4212 [no publications yet] |
Inovio Pharmaceuticals, GeneOne Life Science Inc., DARPA |
Phase 1 | Safety, flexible platform, low cost |
Effective administration requires electroporation technology; requires boost vaccination for immunogenicity |
||
Subunit / Protein |
EBOVGP1,2 with Matrix-M [no publications yet]) |
Novavax | Phase 1 | Pending Phase 1 results, “pro” may be safety |
Immunogenicity unclear at time of publication |
According to https://clinicaltrials.gov.