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New England Journal of Medicine of Publishes Interim Results from Phase 1 Study of Moderna's mRNA Vaccine Against COVID-19
15 July 2020 - - An interim analysis of the open-label Phase 1 study of US-based biotechnology company Moderna, Inc's (NASDAQ: MRNA) mRNA-1273, its vaccine candidate against COVID-19 has been published in The New England Journal of Medicine, the company said.

This interim analysis evaluated a two-dose vaccination schedule of mRNA-1273 given 28 days apart across three dose levels (25, 100, 250 µg) in 45 healthy adult participants ages 18-55 years, and reports results through Day 57.

Results from participants in the initial dose cohorts who received both vaccinations and were evaluated at pre-specified timepoints reaffirm the positive interim data assessment announced on May 18th and show mRNA-1273 induced rapid and strong immune responses against SARS-CoV-2.

The study was led by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health.

mRNA-1273 was generally safe and well-tolerated, with no serious adverse events reported through Day 57. Adverse events were generally transient and mild to moderate in severity.

The most notable adverse events were seen at the 250 µg dose level, with three of those 14 participants reporting one or more severe events.

Solicited systemic adverse events were more common after the second vaccination and occurred in seven of 13 participants in the 25 µg group, all 15 participants in the 100 µg group and all 14 participants in the 250 µg group.

The most commonly reported systemic adverse events following second vaccination at the 100 µg dose were fatigue, chills, headache and myalgia, all of which were transient and mild or moderate in severity.

The most common solicited local adverse event at the 100 µg dose was pain at the injection site, which was also transient and mild or moderate in severity.

Evaluation of clinical safety laboratory values grade 2 or higher and unsolicited adverse events revealed no patterns of concern.

mRNA-1273 induced binding antibodies to the full-length SARS-CoV-2 Spike protein (S) in all participants after the first vaccination, with all participants seroconverting by Day 15.

Dose dependent increases in binding titers were seen across the three dose levels, and between prime and boost vaccinations within the dose cohorts.

After two vaccinations, at Day 57, geometric mean titers exceeded those seen in convalescent sera obtained from 38 individuals with confirmed COVID-19 diagnosis.

Of the 38 individuals in the convalescent sera group, 15% were classified as having severe symptoms (hospitalization requiring intensive care and/or ventilation), 22% had moderate symptoms and 63% had mild symptoms.

Convalescent sera samples were tested using the same assays as the study samples.

Neutralizing activity was assessed in two different assays, a live SARS-CoV-2 plaque-reduction neutralization test and a pseudovirus neutralization assay (pseudotyped lentivirus reporter single-round-of-infection neutralization assay, PsVNA).

No participants had detectable live SARS-CoV-2 virus neutralization or PsVNA responses prior to vaccination.

After two vaccinations, mRNA-1273 elicited robust neutralizing antibody titers. At Day 43, neutralizing activity against SARS-CoV-2 (PRNT80) was seen in all evaluated participants.

At the Phase 3 selected dose of 100 µg, the geometric mean titer levels were 4.1-fold above those seen in reference convalescent sera.

After the second vaccination, PsVNA neutralizing antibody titers were detected in all participants in all dose cohorts. The Day 57 geometric mean titers at the 100 µg dose were 2.1-fold higher than those seen in convalescent sera 3.

Strong correlations were observed between the binding and neutralization assays, and between the live virus and pseudovirus neutralization assays.

A clear dose response was seen in geometric mean titers between the 25 µg and 100 µg dose levels, with minimal additional increases at the 250 µg dose.

T-cell responses were also evaluated at the 25 µg and 100 µg dose levels. Following second vaccination, mRNA-1273 elicited Th1-biased CD4 T-cell responses without significant elevation of Th2-biased CD4 T-cell responses.

Evaluation of the durability of immune responses is ongoing, and participants will be followed for one year after the second vaccination, with scheduled blood collections throughout that period.

An additional seven cohorts in this Phase 1 study have completed enrollment: a 50 µg cohort in adults 18-55, three cohorts of older adults (n=30, ages 56-70, 25 µg, 50 µg, and 100 µg) and three cohorts of elderly adults (n=30, ages 71 and above, 25 µg, 50 µg, and 100 µg).

These data are expected to be published separately. Given the increased morbidity and mortality of COVID-19 in older and elderly adults, additional evidence for the potential of a vaccine to protect this population is an urgent priority.

Both cohorts, healthy adults ages 18-55 years (n=300) and older adults ages 55 years and above (n=300), in the company's Phase 2 study of mRNA-1273 are fully enrolled. This Phase 2 placebo-controlled, dose-confirmation study is evaluating the safety, reactogenicity and immunogenicity of two vaccinations of mRNA-1273 given 28 days apart. Each participant is receiving placebo, a 50 μg or a 100 μg dose at both vaccinations.

The Phase 3 study protocol has been reviewed by the US Food and Drug Administration and is aligned to recent FDA guidance on clinical trial design for COVID-19 vaccine studies. The randomized, 1: 1 placebo-controlled trial is expected to include approximately 30,000 participants at the 100 µg dose level in the US The primary endpoint will be the prevention of symptomatic COVID-19 disease.

Key secondary endpoints include prevention of severe COVID-19 disease (as defined by the need for hospitalization) and prevention of infection by SARS-CoV-2.

The primary efficacy analysis will be an event-driven analysis based on the number of participants with symptomatic COVID-19 disease. The target vaccine efficacy against COVID-19 for powering assumptions is 60% (95% confidence interval to exclude a lower bound >30%).

Data will be reviewed by an independent Data Safety Monitoring Board organized by NIH. The trial is expected to have two interim analyses (at approximately 53 and 106 events), prior to a final event-driven analysis, at approximately 151 events.

The primary efficacy analysis will be an event-driven analysis based on the number of participants with symptomatic COVID-19 disease. This Phase 3 study has been named the COVE study.

The ClinicalTrials.gov identifier is NCT04470427. Registration for the COVE study is expected to be available at study centers across the country beginning on July 21 with study initiation on July 27.

Moderna is working closely with Operation Warp Speed and the NIH, including NIAID's COVID-19 Prevention Trials Network (COVPN), to conduct the Phase 3 COVE study.

Working together with collaborators like NIH, the company hopes to achieve a shared goal that the participants in the COVE study are representative of the communities at highest risk for COVID-19 and of our diverse society.

Moderna has completed manufacture of vaccine required to start the Phase 3 study. With the Phase 3 dose being finalized at 100 μg, the company remains on track to be able to deliver approximately 500 m doses per year, and possibly up to 1 bn doses per year, beginning in 2021 from the company's internal US manufacturing site and strategic collaboration with Lonza.

In addition, Moderna recently announced a collaboration with Catalent for large-scale, commercial fill-finish manufacturing of mRNA-1273 at Catalent's biologics facility in Indiana.

On July 9, Moderna announced a collaboration with ROVI for large-scale, commercial fill-finish manufacturing of mRNA-1273 intended in principle to supply markets outside of the US starting in early 2021 at ROVI's facility in Madrid, Spain.

Funding from the Biomedical Advanced Research and Development Authority (BARDA), a division of the Office of the Assistant secretary for Preparedness and Response within the US Department of Health and Human Services, partially supported the planning for the Phase 2 and Phase 3 studies of mRNA-1273 and is supporting the execution of these studies, as well as the manufacturing process scale-up of mRNA-1273.

Moderna will also fund costs required to complete the development of mRNA-1273 including portions of the Phase 3 study and the scale up of manufacturing capacity at the final established dosage in order to obtain licensure for mRNA-1273.
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