Financial Performance - Revenues for Q1 2025 were 89.0million,asignificantincreasefrom15.6 million in Q1 2024, primarily due to 71.8millionoflicenseandservicerevenuefromthecollaborationwithNipponShinyaku[13]−NetincomeforQ12025was6.1 million, or 0.12pershare,comparedtoanetlossof63.3 million, or 1.38pershare,inQ12024[17]−TotalrevenuesforQ12025reached89,012,000, a significant increase of 469% compared to 15,622,000inQ12024[26]−Licenseandroyaltyrevenuesurgedto87,049,000, up from 15,344,000inthesameperiodlastyear,markingagrowthof4670.12 in Q1 2025, compared to a loss of 1.38pershareinQ12024[26]−Thecompanyreportedacomprehensiveincomeof6,062,000 for Q1 2025, compared to a comprehensive loss of 62,130,000inQ12024[26]CashandAssets−Cash,cashequivalents,andmarketablesecuritiestotaled272.7 million as of March 31, 2025, up from 244.9millionattheendof2024,mainlyduetoa110 million upfront payment from the Nippon Shinyaku partnership[12] - Total current assets increased to 313,237,000asofMarch31,2025,comparedto278,001,000 at the end of 2024, reflecting a growth of 12.7%[25] - Total assets rose to 490,929,000,upfrom465,989,000 at the end of 2024, indicating a growth of 5.3%[25] - Total liabilities increased to 216,732,000from206,338,000, representing a rise of 5.7%[25] Expenses - Research and development expenses for Q1 2025 were 53.1million,adecreasefrom54.8 million in Q1 2024, primarily due to lower clinical trial expenses[15] - General and administrative expenses increased to 20.3millioninQ12025from18.3 million in Q1 2024, mainly due to higher personnel-related costs[16] - Total operating expenses decreased to 76,885,000inQ12025from79,485,000 in Q1 2024, a reduction of 3.9%[26] Clinical Development - The pivotal trial for RGX-202 in Duchenne muscular dystrophy is more than half enrolled, with completion expected in 2025 and a Biologics License Application (BLA) submission planned for mid-2026[5] - REGENXBIO expects to initiate commercial supply manufacturing for RGX-202 in Q3 2025, with all production sourced in the U.S.[6] - The FDA is expected to accept the BLA for clemidsogene lanparvovec (RGX-121) in May 2025, with potential approval in the second half of 2025[14] Partnerships - The partnership with Nippon Shinyaku includes an upfront payment of 110millionandpotentialadditionalpaymentsofupto700 million upon achieving certain milestones[11] - REGENXBIO's cash runway is expected to fund operations into the second half of 2026, excluding potential milestone payments and monetization of a Priority Review Voucher[18]