Financial Performance - Total revenues for Q1 2025 were 517,000,with147,000 from the initial U.S. commercial launch of Symvess and 370,000fromaresearchcollaboration[11].−NetincomeforQ12025was39.1 million, compared to a net loss of 31.9millioninQ12024,largelyduetoanon−cashremeasurementofthecontingentearnoutliability[11].−TotalrevenueforQ12025was517,000, compared to 0inQ12024,indicatingasignificantgrowth[27].−Productrevenuewas147,000, while contract revenue was 370,000,bothcontributingtothetotalrevenue[27].−Operatingexpensesdecreasedto23,701,000 in Q1 2025 from 26,578,000inQ12024,reflectingareductionofapproximately1139,139,000, a turnaround from a net loss of 31,896,000inQ12024[27].−Netincomepershare,basic,was0.28 in Q1 2025, compared to a loss of 0.29pershareinQ12024[27].CashandAssets−AsofMarch31,2025,Humacytereportedcash,cashequivalents,andrestrictedcashof113.2 million[11]. - Cash and cash equivalents increased to 62,847,000asofMarch31,2025,upfrom44,937,000 at the end of 2023[29]. - Total assets rose to 162,553,000asofMarch31,2025,comparedto137,872,000 at the end of 2023, marking an increase of approximately 18%[29]. - Total liabilities decreased significantly to 126,510,000from190,541,000, indicating a reduction of about 34%[29]. - Stockholders' equity improved to 36,043,000asofMarch31,2025,comparedtoadeficitof52,669,000 at the end of 2023[29]. Cost Management - The company implemented cost reduction measures, including a workforce reduction of approximately 31 employees, expected to save about 13.8millionin2025andupto38.0 million in 2026[7]. - Research and development expenses for Q1 2025 were 15.4million,downfrom21.3 million in Q1 2024, primarily due to decreased materials costs[11]. Product Development and Market Approval - 45 hospitals have initiated the Value Analysis Committee (VAC) approval process for Symvess, with five hospitals already approving its purchase[4]. - A total of 84 patients have been enrolled in the V012 Phase 3 clinical trial for dialysis, with an interim analysis planned upon reaching the one-year follow-up for the first 80 patients[8]. - Humacyte plans to file an Investigational New Drug (IND) application with the FDA for first-in-human clinical testing of the small-diameter ATEV in coronary artery bypass grafting (CABG) later this year[8]. Economic Value - The economic value of Symvess is projected to be lower than that of synthetic grafts, with significant cost savings attributed to reduced amputation and infection rates[8]. - The company reported a change in fair value of contingent earnout liability of 49,731,000inQ12025,comparedtoalossof4,593,000 in Q1 2024[27].