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A candidate vaccine for Covid-19 developed by the drug maker Moderna appears to generate an immune response similar to the response seen in people who have been infected by the virus and recovered, the company said Monday.

In a Phase 1 trial, eight patients who received two doses of the vaccine at the lowest and middle doses tested — 25 and 100 micrograms — developed neutralizing antibodies to the virus at levels similar to people who had recovered from infection, the company said in a statement.

The data were limited and from only a small number of participants in the trial, led by the National Institute of Allergy and Infectious Diseases. But they are still likely to be seen as encouraging. Research aimed to develop a vaccine against SARS, a related virus responsible for a 2002-2003 outbreak, showed that neutralizing antibodies are pivotal for achieving protection.


Moderna is developing the vaccine in conjunction with the NIAID’s Vaccine Research Center.

“These interim Phase 1 data, while early, demonstrate that vaccination with mRNA-1273 elicits an immune response of the magnitude caused by natural infection starting with a dose as low as 25 μg,” said Tal Zaks, Moderna’s chief medical officer.


The statement noted that a new arm of the trial is being established to test a 50-microgram dose, which may suggest concern that the 25-microgram dose may be too low.

As the vaccine’s developers work to establish a dose, they must balance the need to achieve protection in individuals — including seniors, who are at highest risk in this pandemic but whose immune systems do not respond as well to vaccines — with the goal of using as little vaccine as possible per person to stretch out what will be limited supplies.

“I think 25 [micrograms] gets us there but you always want to have somewhat of a margin,” Zaks told STAT in an interview.

“The sense is at the end of the day we’re going to narrow it down on somewhere between 25 and 100,” he said. “It’s going to be really hard math for us.”

While some experts wanted more detail before commenting on the data, others saw it as a positive sign for this vaccine.

“The neutralizing antibody and safety results from the Phase 1 clinical study are promising for the Moderna mRNA vaccine candidate and supportive to proceed forward with the planned Phase 2 studies,” Robin Robinson, chief scientific officer at RenovaCare, told STAT. Robinson is a former director of the Biomedical Advanced Research and Development Authority.

Vaccination with the candidate vaccine, provisionally labeled mRNA-1273, also prevented viral replication in the lungs of mice in preclinical testing, the company’s statement said.

A Phase 2 trial has already been given the go-ahead by the Food and Drug Administration. CEO Stéphane Bancel said the company is pushing forward with a Phase 3 trial set to start in July and is ramping up its capacity to manufacture the vaccine.

“We are investing to scale up manufacturing so we can maximize the number of doses we can produce to help protect as many people as we can from SARS-CoV-2,” Bancel said, referring to the virus that causes Covid-19.

The company’s statement suggested the vaccine was well-tolerated in people who received it in the Phase 1 dosing trial. One of the people in the 100-microgram arm developed redness at the injection site that met the criteria for a Grade 3 adverse event. And three volunteers in the highest dose arm — 250 micrograms — developed Grade 3 systemic reactions after receiving the second of two doses. There were no Grade 4 or life-threatening adverse events recorded in the trial.

The early readout included arms of the trial involving people ages 18 to 55 years old who received either two doses at the 25 microgram or 100 microgram level or one dose at 250 microgram. There were 45 people involved in these three arms, though neutralizing antibody data are only available at this point for the first four patients each of the 25 microgram and 100 microgram cohorts.

People who received two doses at the 25 microgram level developed binding antibodies at levels consistent with those seen in the blood of people who have recovered from Covid-19 infection, the statement said. People who received two doses at 100 microgram had binding antibody levels that “significantly exceeded” the levels seen in the blood of Covid-19 survivors.

  • Certainly good news!

    One thing that is concerning is that Moderna did not quantify the neutralizing titers produced by vaccination, they only equated the response to those observed in recovered patients. As COVID produces a wide range of clinical symptoms from asymptomatic to fatal, it is important to know what type of patients they are making the comparison to- Asymptomatic patients? Intubated Patients? etc.

    There has been plenty of data revealed to date showing that recovered patients have a wide range of neutralizing antibody responses, with those with mild infections generally reported to have lower titers.l than those that were seriously ill.

  • What are the side effects from the early trial testing? How long are they monitoring these people who have been given this so called vaccine? Rushing to get a vaccine for a virus they have no ideal on how to fight against can lead to more people dying from them testing to get a vaccine. When getting vaccines in the past it wasn’t a hurry up and rush because people where important back then and they had casualties but it wasn’t a hurry up and rush process. It’s all about the rich getting rich and that is why so many people are dying in the first place. It doesn’t have to do with color, race, age or status the covid 19 virus is killing every and anybody who is not able to fight it off in their system. Please answer my questions and thank you for your response.

    • This vaccine model was already tested for Sars cov and there are people out there who had it during the first phases of those trials. Since Sars cov was contained and quit spreading the trials didnt/couldn’t finish. They just tweaked that vaccine to work for this vaccine. That’s why the trials are moving along as quickly as they are. The safety was already pretty well documented. It’s the efficacy they couldn’t account for.

      All the vaccines currently already in human trial are just tweaked versions of the original Sars or mers vaccines.

    • You’re right. Let’s just throw in the towel and forget science and modern innovation. If it wasn’t done in the past it can’t be done now. Nobody who is rich has died or was close to anyone who died from covid.

      You’re likely a liberal.

  • Can you ask your Lord Jesus why didn’t he stop the holocaust, stop the all the pandemics for the last thousand years, end starvation in poor countries, stop the abuse of children around the world, save animals for being slaughtered for trophies or for fun, cure for cancer, diabetes, etc? I want to know why? If I was GOD, I would make this whole world peaceful and loving place to live! I wouldn’t want to see anyone or anything suffer.

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