Table 2.
The most recently registered clinical trials for RSV vaccines, prophylactics and therapeutics since 2008
Drug name | Clinical trial status | Manufacturer/Institution | Experimental approach | Outcome |
---|---|---|---|---|
Vaccines | ||||
Live attenuated | ||||
MEDI-559 | Phase 1/2a | MedImmune LLC | Live attenuated | Increased rate of LRTIs in vaccine recipients, further study ongoing |
RSV LID ΔM2-2 | Phase 1 | NIAID | Recombinant live attenuated RSV | Estimated completion May 2016 |
RSV cps2, Lot RSV#005A | Phase 1 | MedImmune, NIAID | Recombinant live Attenuated RSV | Estimated completion May 2015 |
Chimeric/vectored | ||||
RSV 001 | Phase 1 | Okairos | Adenovirus vector and an MVA vector encoding RSV antigens | Commenced May 2013 |
Outcome awaited | ||||
MEDI-534 | Phase I | MedImmune LLC | Chimeric/vectored | Genetic variants within vaccine detected. Ongoing research. |
Nanoparticle | ||||
RSV F nanoparticle vaccine | Phase 2 | Novavax | Recombinant RSV F protein particle | Commenced October 2013 Outcome awaited |
Subunit | ||||
MEDI 7510 | Phase 1a | MedImmune LLC | RSV sF antigen + synthetic glucopyranosyl lipid A adjuvant | Estimated completion July 2015 |
RSV F subunit vaccine | Phase 1 | Novartis vaccines | F subunit vaccine | Estimated completion September 2016 |
GSK3003891A | Phase 1 | GlaxoSmithKline (GSK) Biologicals | Prefusion F subunit vaccine | Estimated completion March 2015 |
Prophylactics | ||||
Motavizumab (Numax/MEDI-524) | Phase 3 (completed 2008) | MedImmune | Affinity-matured palivizumab | Increased type I hypersensitivity. |
No FDA approval | ||||
MEDI 557 | Phase 1 | MedImmune | Recombinant human monoclonal antibody | Completed May 2013. Data not available |
MEDI 8897 | Phase 1b/2a | MedImmune | Human RSV monoclonal antibody | Estimated completion December 2014 |
RI-001 | Phase 2 | ADMA biologics Inc | Polyclonal immune globulin. Delivered intravenously | Completed May 2010 |
REGN2222 | Phase 3 | Regeneron pharmaceuticals | Human monoclonal anti-RSV F antibody | Estimated completion date February 2015 |
Therapeutics | ||||
GS-5806 | Phase 2b | Gilead | RSV entry inhibitor | Estimated completion June 2015 |
ALN-RSV01 | Phase 2b (completed May 2012) | Ablynx | siRNA targeting the N protein | Reduced bronchiolitis obliterans post-RSV infection in lung transplant recipients. |
ALS-008176 | Phase 2a | Alios biopharma Inc. | Nucleoside analogue | Estimated completion August 2014 |
Danirixin | Phase 1 | GlaxoSmithKline | CXCR2 antagonist. | Estimated completion July 2014 |
Inhibition of neutrophil activation | ||||
RV568 | Phase 1 | Respivert Ltd | Kinase inhibitor | Completed 2011. Data not available |
MDT-637 | Phase 1 | MicroDose Therapeutx, Inc | Fusion inhibitor | Commenced 2013. Data not available |
ALX-0171 | Phase 1 | Ablynx | Nanobody | Commenced 2014 |
Data not available |