|Videos|May 11, 2020

The Pursuit of a COVID-19 Vaccine

Preventive medicine expert William Schaffner, MD, discusses what it will take for investigators to properly assess and manufacture a vaccine.

This month has been marked by clinical launches for potential coronavirus 2019 (COVID-19) vaccines.

Investigators from the University of Oxford began testing a potential vaccine in 1100 volunteer patients, while the vaccine undergoes early mass manufacturing in hopes early results show benefit.

The ChAdOx1 nCoV-19 is comprised of genetic material used to make Spike glycoproteins, a surface protein from SARS-CoV-2 that plays an essential role in the virus’ binding to ACE2 inhibitors and eventual infection of the person.

A week later, Pfizer and BioNTech announced first dosing for a phase 1/2 clinical trial assessing mRNA vaccine candidate in global patients stratified by age groups.

The investigators are hoping to simultaneously evaluate the 4 different mRNA candidates while sharing data with regulatory authorities in real-time—streamlining the process from identifying a safe and viable vaccine, and it reaching the public market.

Another mRNA candidate, mRNA-1273 from Moderna, will be assessed as 2 different doses in 600 participants versus placebo—with hope and expectation of federal support that it will reach phase 3 trial analysis in the Fall.

What is there to make of all these differing candidates? What’s the value of different trial designs? What is a realistic timeline for results?

Answers to these questions are highly dependent on what is learned from clinical results, but a lot could be learned from previous prophylaxis development.

In an interview with Contagion, William Schaffner, MD, professor of Preventive Medicine and Medicine at the Vanderbilt University Medical Center, discussed the finer details of these vaccine candidates and their trial makeup—and gave perspective as to what people should expect in the coming months.

Namely, is it reasonable to begin manufacturing a vaccine for a pandemic disease before it’s known whether it works?

“It’s a little like a horse race,” he said. “The horses haven’t gone around the track yet, but you put your money down.”


Related to this article

Cefiderocol Continues to Show Activity Against Resistant Gram-Negative Infections
Shionogi data presented at IDWeek 2026 demonstrated a 76.7% clinical response with cefiderocol in carbapenem-resistant respiratory infections and high in vitro activity against resistant P aeruginosa VAP isolates. Christine Slover, PharmD, vice president, Infectious Diseases US Medical Affairs, Shionogi, offers insights on the data as well as clinical considerations for providers when weighing the antibiotic for patients.
Pfizer 25-Valent Pneumococcal Vaccine Boosts Serotype 3 Response in Infants
Alejandra Gurtman, MD, discussed the phase 2 data at IDWeek 2026 which showed the investigational 25-valent pneumococcal conjugate vaccine 25vPnC produced serotype 3 antibody levels about 15-fold higher than Prevnar 20 after the booster dose, targeting a serotype still behind 10.6% of invasive pneumococcal disease in US children younger than five years.
Household Contacts Drive Most Hepatitis B Exposures in Young Children
Karen B. Jacobson, MD, MPH, of Kaiser Permanente Northern California, presented data at IDWeek 2026 showing 58.2% of children younger than five years exposed to active hepatitis B in the home were exposed by someone other than their birth mother, a risk maternal screening alone would miss under the CDC’s revised birth dose recommendation.