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. 2020 Jun 18;35:43–49. doi: 10.1016/j.prrv.2020.06.010

Table 1.

Candidate COVID-19 vaccines currently in phase 1 or 2 human clinical trials.

Platform Description Advantages Disadvantages
Recombinant Viral vector Unrelated virus engineered to encode the target gene of the pathogen. Viral vectors can be replicating or non-replicating Induces high cellular and humoral immune responses Possible pre-existing immunity against vector
Risk of reversion to virulence
Limitations in scaling-up production
Candidate vaccines: Ad5-CoV
Adenovirus Type 5 vector; antigen: Spike protein
Phase I: CanSino Biologics ChiCTR2000030906 [88]/NCT04313127 [89]
Phase II: Institute of Biotechnology; Academy of Military Medical Sciences
ChiCTR2000031781 [90]/NCT04341389 [91]
Participants: 18–60 years; Phase I n = 108Phase II: n = 508
Phase I: vaccine was safe and tolerable. No serious adverse effects. 63 participants (Low dose n = 18 [50%); moderate dose n = 18 [50%]; high dose n = 27 [75%]) developed four fold rise in neutralising antibody titres by Day 28. Pre-existing immunity to Ad5 neutralising antibody titre was observed in half of the participants before vaccination. Out of these, a low proportion seroconverted[76], [1]

AZD1222 (previous known as ChAdOx1 nCoV-19)
Simian adenoviral vaccine vector; antigen: Spike protein
Phase I/II: University of Oxford NCT04324606 [92]
Participants: 18–55 years; n = 1090
Inactivated Pathogen virus inactivated by chemicals or radiation Easy to prepare
High safety
Variable efficacy
Candidate vaccines: PiCoVacc
Phase I/II: Sinovac Biotech Co NCT04352608 [93]
Participants: 18–59 years; Phase I n = 144; Phase II n = 600

Phase I/II: Sinovac Biotech Co NCT04383574 [94]
Participants: ≥60 years; Phase I n = 72; Phase II n = 350
Inactivated novel coronavirus vaccine
Phase I/II: Beijing Institute of Biological Products/Sinopharm
ChiCTR2000032459 [95]
Recruitment: Age >/= 3 years; Phase I n = 480; Phase II n = 1168

Inactivated novel coronavirus vaccine
Phase I/II: Wuhan Institute of Biological Products/Sinopharm
ChiCTR2000031809 [95]
Participants: Age >/= 6 years; Phase I n = 288; Phase II n = 1168
Live attenuated Live virus whose genome(s) is mutated, inducing immune response but not disease Induces long-term immunity Expensive to produce
Candidate vaccines: Nil in clinical trials as yet
Protein subunit Components of target antigen protein produced in laboratory; some vaccines may use nanoparticle technology High safety
Scalability
High cost
Lower immunogenicity and may require adjuvant or repeat doses
Candidate vaccines: NVX-CoV2373
Phase I: Novovax NCT04368988 [96]
Participants: 18–59 years; n = 131
Virus like particle Non-infectious self- assembling viral structural proteins Induces strong immune response Limitations in manufacturing production
Candidate vaccines: Nil in clinical trial as yet
mRNA mRNA encoding target antigen (may be complexed with lipid- or polymer-based nanoparticles) Easier to design
Induces strong immune response
Rapid manufacture
Requires mRNA to be encapsulated otherwise unstable under physiological conditions
Candidate vaccines: BNT162
Phase I/II: BioNTech/Pfizer
Four candidates, two candidates include a nucleoside modified mRNA, one a uridine containing mRNA and the fourth self- amplifying mRNA. Each combined with a lipid nanoparticle formulation.

Germany 2020–001038-36 [97]
Participants: 18–55 years; n = 196

USA NCT04368728 [96]
Participants: 18–85 years; n = 7600

mRNA-1273
Lipid nano-particle (LNP)-encapsulated mRNA vaccine;
Coding antigen: full length S-protein
Phase I/II: Moderna/National Institute of Allergy and infectious diseases
NCT04283461 [59]
Participants: 18–55 years, extended to 99 years n = 155
Interim Phase 1 Data: 15 participants seroconverted by day 15; 8 participants: all developed neutralizing antibodies[77]
DNA DNA that encodes the target antigen Easier to design
Rapid manufacture
May require a special approach to administer the vaccine (e.g. electroporation device)
May requires adjuvant Uncertainty of safety issues
INO-4800
Phase I: Inovio Pharmaceuticals NCT04336410 [98]
Participants : 18–50 years n = 40

Plasmid DNA oral vaccine (bacTRL-IL-Spike-1)
Phase 1: Symvivo NCT04334980 [99]
Participants: 19 = 55 years; n = 84