Hansoh Pharma says Phase III LIGHTEN trial shows 19.3% weight loss at week 48 with olatorepatide 15 mg

• Hansoh Pharma reported Phase III LIGHTEN results for olatorepatide at EASD 2026 in Milan as a late-breaking oral presentation.
• The China study showed clinically meaningful weight loss over 48 weeks, with continued reduction suggesting no plateau by study end.
• Safety looked consistent with the incretin class, with generally favorable gastrointestinal tolerability and no treatment-related discontinuations reported.
• The readout supports olatorepatide’s positioning as a potential new weight-management drug, strengthening Hansoh’s late-stage metabolic pipeline.

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