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Wall M (2017) Update on idiopathic intracranial hypertension
Lilly plans to complete seven additional Phase 3 trials in 2026, covering applications from sleep apnea to liver disease, before filing for FDA approval
The active ingredient itself (tirzepatide) has extensive FDA-approved clinical data behind it
Lack of dosing safety studies: Even small differences in dose may lead to drastically different outcomes due to its extreme potency
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