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Based on the Phase 2 results and the speed of Eli Lillys development timeline, analysts expect an FDA submission sometime in 2025 or 2026, with potential approval following 12 to 18 months after submission if the data holds
Your provider starts you on the lowest effective dose and gradually increases it to minimize side effects
Inflammatory macrophage memory in nonsteroidal anti-inflammatory drugexacerbated respiratory disease
Common patterns from user reports include substantial appetite suppression within the first week or two of treatment, meaningful weight loss averaging around 10% of starting body weight by month three, the phenomenon users describe as a "whoosh" of accelerated weight loss after each dose escalation, and significant psychological relief from constant food-related thoughts
Visible changes: noticeable to people around you, clothing sizes may change
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