Reuters Vaccine Tracker
| Developer/country | Vaccine
  type | Seroconversion
  Rate | Protective
  Efficacy | Status | 
| Pfizer/BioNTech
  – US/Germany | mRNA
  spike LNP | 95.2% CD4+ T cell  | Full FDA Approval Dec 10, 2021 | |
| Moderna/NIAID
  - US Prescribing info | 94.1% after 2 doses | |||
| Oxford/Astra
  Zeneca - UK | Chimp adenovirus vectors - spike  | Germany approve use only in under 65s due to lack of data Over 65s now getting it preferentially due to blood clots in younger subjects. | 70.4% overall | Several countries hold off due to rare blood clots.   | 
| Gamaleya (Russia) | Human adenovirus vector - 2 spike | 91.4% after 2 doses Lancet | ||
| CureVac (Germany) | May cover variants - no need for sub-zero | Deal w/UK to focus on variants | EU begins review 03/21 | |
| Sanofi/Translate Bio | mRNA | 1 or 2 doses | Phase 1/2 Trials initiated 03/21 | |
| Sanofi/GSK | 89.6%
  18-49 yo | Delayed due to poor response in older subjects 11/12/20 | ||
| Novavax  (Nuvaxovid, CovoVax) | rDNA/Matrix-M™
  adjuvant: Production by India's SII the world's largest producer of vaccines by volume | 100% after dose 2 96.4% effective against original strain in UK trial, 86% UK, 55% SA strains 
 | 89.3% in US/Mex 60% in SA in HIV neg subj | Delayed (Q3) Delayed again (Q4) EMA started a rolling review of NVX-CoV2373 in early 2021 | 
| Sinopharm
  (China) | Inactivated
  virus | 
 | 79.34% | China
  approved Dec31 WHO approved 07-05-21 Clin Trial results JAMA 26/5/21 | 
| Sinovac
  (China) – | Inactivated virus - 2nd vaccine in China | 
 | 50.4% Brazil, 78% Brazil, 65.3% Indonesia, 91.25 Turkey | WHO approval expected 03/21 | 
| J&J
  /Janssen (US) 
   | AdVac® human attenuated adenovirus vectors
  carrying complete spike protein rDNA | 98% After 1 dose, 100% in interim results 1 vs 2 dose trial | enrolment completed - | US approved Jan 27 EU applied 16/02/21 EU approved 11-03-21 Merck/Sanofi/others to help manufacture, fill & pack J&J temp suspended release due to rare blood clots in younger, mostly women. | 
|  | Combination vaccine - recombinant nanoparticle protein-based COVID-19 and NanoFlu™ vaccines with Matrix-M™ adjuvant |  |  | |
|  |  |  |  |  | 
| APC/Vaxine |  | Phase 2 initiated | Manufacturing
  scale-up in Dublin | |
| Valneva (France)VLA2001 | inactivated adjuvanted whole virus vaccine | 89.8% in the medium-dose and 100% in the high-dose group after 2 doses 95% response | Phase 3 better response than AZ vaccine - sig better tolerability | Phase 3 trial underway Completed and showed superior response to AZ vaccine and good antibody response. | 
| Zydus Cadila  | 1st
  plasmid DNA vaccine (3 dose) |  |  | Clin trials
  in 50 centers | 
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| Multivalent, Multiviral Vaccines | ||||
| Moderna  Quadrivalent
  flu | Phase 1  | GMT
  against all strains at 29 days A/H1N1,
  A/H3N2, influenza B/Yamagata- and B/Victoria-lineages | Phase 3 prep
  underway |  | 
| Moderna mRNA-1011 Multivalent
  flu | Strategic
  planning mRNA |  |  |  | 
| Moderna mRNA-1020 Sars-CoV-2/Flu/RSV
  booster |  |  |  | |
|  | Spike Ferritin Nanoparticle COVID-19 vaccine |  |  | |
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| Veklury
  (remdesivir) | IV 10 days | Shorter time
  to recovery and less progression to severe disease | Viral RNA
  polymerase inhibitor | |
| Lageviro (molnupiravir) | 50 % effective given within 5 days of the onset of symptoms | PO  40 pills over five days | 5 days no
  detectable virus | |
| Yeliva
  (opaganib) | PO | Reduces need
  for oxygen in hospitalised patients | sphingosine
  kinase-2 (SK2) selective inhibitor | |
| upamostat | PO |  | Serine protease
  inhibitor Phase
  2/3 trial | |
| bamlanivimab/etesevimab | IV infusion | Reduces risk
  of hospitalisation and death by 87% | Mab | 
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|  | GlaxoSmithKline (GSK) with U.S. partner Vir |  |  | |
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