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Post-Market Surveillance Gap: Because AOD-9604 never received FDA approval for any indication, there is no post-market surveillance system capturing safety signals from widespread clinical use

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The best choice depends entirely on the dose sizes in your protocol and your comfort level with measuring smaller volumes

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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