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Fat droplet formation decreased, and the cells accumulated less fat even when exposed to conditions that normally promote fat storage

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Purity testing The company states each batch undergoes testing to confirm 99% or greater purity

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the FDA also notes these reports are likely underreported because state-licensed 503A pharmacies are generally not required to submit adverse events to FDA

Inclusion Criteria Exclusion Criteria Timeline for a Trial Participant Screening Participants are screened for eligibility to participate in the trial Treatment Participants receive weekly subcutaneous injections of either CagriSema or Tirzepatide, with a dose escalation period followed by maintenance dosing Follow-up Participants are monitored for safety and effectiveness after treatment What Are the Treatments Tested in This Trial