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Lexeo Therapeutics(LXEO) - 2024 Q4 - Annual Results
LXEOLexeo Therapeutics(LXEO)2025-03-24 11:01

Financial Performance - Lexeo Therapeutics reported a net loss of 25.9millionor25.9 million or 0.78 per share for Q4 2024, compared to a net loss of 14.2millionor14.2 million or 0.86 per share for Q4 2023 [10]. - For the full year 2024, the net loss was 98.3millionor98.3 million or 3.09 per share, compared to a net loss of 66.4millionor66.4 million or 12.40 per share for 2023 [10]. - General and administrative expenses rose to 9.0millionforQ42024,comparedto9.0 million for Q4 2024, compared to 6.8 million in Q4 2023, with total expenses for the year reaching 31.7million,upfrom31.7 million, up from 15.4 million in 2023 [10]. Research and Development - Research and development expenses increased to 18.4millionforQ42024,upfrom18.4 million for Q4 2024, up from 8.2 million in Q4 2023, and totaled 74.1millionfortheyear,comparedto74.1 million for the year, compared to 53.1 million in 2023 [10]. - Interim update from cohort 1 of the LX2020 HEROIC-PKP2 trial showed 71% and 115% increases in PKP2 protein expression from baseline [10]. - The first participant evaluated 6 months post-treatment experienced a 67% reduction in premature ventricular contractions (PVCs), decreasing from 861 to 284 [10]. - Enrollment for cohort 2 of the LX2020 HEROIC-PKP2 trial has been completed, with interim clinical data expected in the second half of 2025 [10]. - Lexeo Therapeutics anticipates further regulatory clarity for LX2006, including the inclusion of pediatric cohorts in the planned pivotal study [10]. Cash Position - Cash, cash equivalents, and investments as of December 31, 2024, were $128.5 million, expected to fund operations into 2027 [10]. Regulatory Developments - The European Commission granted orphan medicinal product designation for LX2020 for the treatment of PKP2-ACM in March 2025 [10].