AT1001 for the Treatment of COVID-19 Related MIS-C

This is a registry record, not a result. A trial being listed, recruiting or completed says nothing by itself about whether the compound works or is safe.

Registry numberNCT05022303
StatusTerminated
PhasePhase 2
SponsorMassachusetts General Hospital
Enrollment12 participants
DesignInterventional, Randomized, Parallel, Masking: Double
ConditionsCovid19; Multisystem Inflammatory Syndrome in Children
InterventionsLarazotide Acetate; Placebo
StartOct 1, 2021
Primary completionMay 15, 2024
Study completionMay 15, 2024
Results postedNot yet
Registry last updatedJun 13, 2024

Compounds on this site that cite this trial

What the registry says the trial is about

The primary aim of this study is to evaluate the efficacy and safety of AT1001 versus placebo in pediatric patients with SARS-CoV-2 infection who experience early signs of MIS-C and are at high risk of progression.

AT1001 10 μg/kg/dose up to 500 μg/dose (rounded to the nearest 50 μg) or matching placebo will be administered orally four times a day (QID) to the standard of care for MIS-C.

Primary outcomes

These are what the trial was designed to measure first. They are registered in advance, which is what makes a later result checkable.

Outcome measureTime frame
Evaluate the efficacy and safety of AT1001 versus placebo on mitigating symptoms of MIS-C24 weeks
Determine proportion of participants with improvement in MIS-C related GI symptoms and no progression of disease24 weeks

11 secondary outcomes also registered. See the registry record for the full list.

Source: ClinicalTrials.gov (U.S. National Library of Medicine). Last checked against the registry on Oct 3, 2026. See the trial changes feed for what has changed recently.