AEON gets FDA Type 2b feedback on ABP-450 biosimilar pathway for BOTOX
FDA meeting minutes support a potentially narrower clinical program, with an IND for a pharmacodynamic study planned for the fourth quarter of 2026.
SEC filing
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FDA meeting minutes support a potentially narrower clinical program, with an IND for a pharmacodynamic study planned for the fourth quarter of 2026.
SEC filing
The company reported cash of $3.4 million as of June 30, 2026, plus a July financing that it says extends its runway into early 2027 as it awaits further FDA feedback on its Botox biosimilar.
SEC filing
The biosimilar developer priced and closed an underwritten stock and warrant sale, netting $12.2 million with up to $29.6 million more possible if warrants are exercised.
SEC filing (3)