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Its Phase 3 weight-loss figures (in the low-to-mid 20% range) and its late-2025 FDA filing belong to the combination product, not to standalone cagrilintide, which remains at the Phase 2 stage with a peer-reviewed monotherapy result of about 10.8% at 26 weeks

Phase 2 human trials of full-length Thymosin Beta-4 in pressure ulcers and venous stasis ulcers reported no significant adverse events distinguishable from placebo