Product Development and Approvals - LYTENAVA™ is the first and only approved ophthalmic formulation of bevacizumab for the treatment of wet AMD in the EU and UK, with the first commercial launch anticipated in H1 CY25[2] - The company plans to resubmit the BLA for ONS-5010 in Q1 CY2025, with final efficacy data from NORSE EIGHT expected in January 2025[6][9] - Initial commercial launches of LYTENAVA™ in Europe are planned to commence in H1 CY2025[6] - Potential US FDA approval of ONS-5010 is anticipated in H2 CY2025[6] Financial Performance - Outlook Therapeutics had cash and cash equivalents of 14.9millionasofSeptember30,2024[10]−Thecompanyreportedanetlossof75.4 million, or 4.06perbasicanddilutedshare,forthefiscalyearendedSeptember30,2024,comparedtoanetlossof59.0 million, or 4.72perbasicanddilutedshare,forthepriorfiscalyear[18]−Researchanddevelopmentexpensesincreasedto41.8 million in FY2024 from 26.5millioninFY2023[23]−Generalandadministrativeexpensesincreasedto29.9 million in FY2024 from 26.7millioninFY2023[23]−Totalassetsdecreasedto28.8 million as of September 30, 2024, from 32.3millionasofSeptember30,2023[24]−Totalstockholders′deficitincreasedto73.1 million as of September 30, 2024, from $14.4 million as of September 30, 2023[24]