Key result
Single-dose mRNA-1273.712 does not significantly increase cardiac troponin I levels compared to placebo.
Why the study?
Myocarditis is a very rare event following COVID-19 vaccination, primarily observed in young males, but cardiac troponin I is not etiologically specific; this study evaluated cTnI levels following mRNA-1273.712 vaccination versus placebo in individuals aged 12-30 years.
Does mRNA-1273.712 vaccination increase the incidence of elevated cardiac troponin I compared to placebo in healthy adolescents and young adults aged 12 to 30 years?
RCT (n=1,000)
Observer-blind
1:1 crossover
Yes
Does mRNA-1273.712 vaccination increase the incidence of elevated cardiac troponin I compared to placebo in healthy adolescents and young adults aged 12 to 30 years?
A single 50 μg dose of mRNA-1273.712 in adolescents and young adults is not associated with subclinical cardiac injury, as evidenced by a lack of vaccine-related cardiac troponin I elevations or myocarditis.
Background Myocarditis is a very rare event following COVID-19 vaccination, with highest risk observed in males aged 12–24 years. Cardiac troponin I (cTnI) is a cardiac-specific biomarker of myocardial injury but is not etiologically specific and may be elevated in the absence of cardiac pathology, including after vigorous physical activity. This study assessed cTnI levels following administration of mRNA-1273.712 vaccine versus placebo in participants aged 12–30 years. Methods In this phase 4, observer-blind, randomized, placebo-controlled, crossover study, participants received mRNA-1273.712 50 µg and placebo 28 days apart. cTnI was measured at baseline and 3 and 28 days after injection. The primary endpoint was the proportion of participants with elevated cTnI 3 days after injection. Safety was monitored throughout. Results Of 1000 participants randomized, 981 had evaluable cTnI results; most (>98%) maintained normal cTnI levels at all measured timepoints, including at 3 days post-injection. 18/981 participants had ≥1 elevated cTnI result at any study timepoint; 7 of those 18 had elevations at baseline prior to any injection. Of the remaining 11 participants with normal baselines and no prior elevations, 3 had elevated cTnI 28 days after receiving mRNA-1273.712 and 8 had elevations after placebo. 11/18 participants with elevated cTnI reported recent physical activity, and none exhibited clinical signs or symptoms of myocarditis or pericarditis. No new safety concerns were identified. Conclusions cTnI elevations were low overall and were observed after both placebo and mRNA-1273 administration. Vaccination with mRNA-1273.712 in adolescents and young adults was not associated with elevated cTnI. ClinicalTrials.gov identifier: NCT06634797
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Pfeiffer et al. (2026) conducted an RCT in Healthy individuals (COVID-19 vaccine recipients) (n=1,000). mRNA-1273.712 vs. Placebo was evaluated on Proportion of participants with elevated cTnI levels 3 days after injection (Difference: 0.6%, 95% CI -0.1, 1.4).
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