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Each patient received 5.0 g of Epitalon per eye, injected parabulbarly for 10 consecutive days

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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

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Research Use Only Cagrilintide is supplied strictly for in-vitro laboratory research

Any perceived weight loss benefits typically relate to the correction of deficiency symptomssuch as fatigue and low moodwhich may indirectly improve an individual's capacity for physical activity and dietary adherence