Financial Position - Nuvation Bio reported a strong balance sheet with cash, cash equivalents, and marketable securities totaling 502.7millionasofDecember31,2024[1].−NuvationBio′stotalassetsdecreasedto540.6 million as of December 31, 2024, down from 621.5millionin2023[17].−Theaccumulateddeficitincreasedto910.7 million as of December 31, 2024, compared to 342.8millionin2023[17].RevenueandProfitability−RevenueforQ42024was5,711,000 compared to 0inQ42023,indicatingasignificantincrease[18].−GrossprofitfortheyearendedDecember31,2024,was795,000, up from 0in2023[18].−ComprehensivelossfortheyearendedDecember31,2024,was567,547,000, compared to 70,095,000in2023[18].Expenses−ResearchanddevelopmentexpensesforQ42024were29.3 million, a significant increase from 15.4millioninQ42023,primarilyduetopersonnel−relatedcostsfromtheacquisitionofAnHeartTherapeutics[7].−Selling,general,andadministrativeexpensesroseto26.1 million in Q4 2024, compared to 5.5millioninQ42023,drivenbyincreasedpersonnelandmarketingexpenses[9].−TotaloperatingexpensesforQ42024were55,437,000, a substantial increase from 20,831,000inQ42023[18].−Thecompanyreportedasignificantincreaseintotaloperatingexpensesfortheyear,totaling593,422,000 compared to 99,822,000in2023[18].NetLoss−NuvationBioreportedanetlossof49.4 million, or (0.15)pershare,forQ42024,comparedtoanetlossof13.8 million, or (0.06)pershare,inthesameperiodof2023[10].−NetlossforQ42024was49,445,000, compared to a net loss of 13,787,000inQ42023[18].−NetlosspershareattributabletocommonstockholdersforQ42024was(0.15), compared to (0.06)inQ42023[18].FinancingandFunding−Thecompanysecuredupto250 million in non-dilutive financings from Sagard Healthcare Partners, which includes 150millioninroyaltyinterestfinancingand50 million in debt upon FDA approval of taletrectinib by September 30, 2025[5]. - Interest income for the year ended December 31, 2024, was 27,062,000,upfrom24,611,000 in 2023[18]. Product Development and Regulatory Updates - The FDA accepted and granted Priority Review to the NDA for taletrectinib for advanced ROS1-positive NSCLC, with a PDUFA goal date set for June 23, 2025[3]. - Taletrectinib has been approved by China's NMPA for adult patients with locally advanced or metastatic ROS1+ NSCLC, with Innovent Biologics commercializing the drug in Greater China[8]. - The company launched an Expanded Access Program in the U.S. for taletrectinib in February 2025, allowing eligible patients to access the drug outside of clinical trials[8]. Shareholder Information - The weighted average common shares outstanding increased to 336,934 in Q4 2024 from 218,993 in Q4 2023[18].