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Nuvation Bio (NUVB) - 2024 Q2 - Quarterly Results
NUVBNuvation Bio (NUVB)2024-08-05 12:37

Financial Performance - Nuvation Bio reported a net loss of 462.5million,or462.5 million, or (1.89) per share, for Q2 2024, compared to a net loss of 20.6million,or20.6 million, or (0.09) per share, for the same period in 2023[6]. - Revenue for the three months ended June 30, 2024, was 1,435,000,comparedto1,435,000, compared to 0 for the same period in 2023[12]. - Gross profit for the three months ended June 30, 2024, was 88,000,indicatingagrossmarginofapproximately6.188,000, indicating a gross margin of approximately 6.1%[12]. - Total operating expenses increased significantly to 470,473,000 for the three months ended June 30, 2024, compared to 26,131,000forthesameperiodin2023[12].NetlossforthethreemonthsendedJune30,2024,was26,131,000 for the same period in 2023[12]. - Net loss for the three months ended June 30, 2024, was 462,492,000, compared to a net loss of 20,640,000forthesameperiodin2023,representinganincreaseinlossofapproximately2,23720,640,000 for the same period in 2023, representing an increase in loss of approximately 2,237%[12]. Research and Development - Research and development expenses for Q2 2024 were 29.2 million, up from 18.6millioninQ22023,primarilyduetoa18.6 million in Q2 2023, primarily due to a 5.9 million increase in personnel-related costs and a 4.7millionincreaseinthirdpartyresearchservices[5].ResearchanddevelopmentexpensesforthethreemonthsendedJune30,2024,were4.7 million increase in third-party research services[5]. - Research and development expenses for the three months ended June 30, 2024, were 29,247,000, up from 18,590,000forthesameperiodin2023,reflectingagrowthofapproximately57.318,590,000 for the same period in 2023, reflecting a growth of approximately 57.3%[12]. - Nuvation Bio has decided not to initiate a Phase 2 study of NUV-868 in solid tumor indications after reviewing data from earlier studies[4]. - The global Phase 2 study of safusidenib for diffuse IDH1-mutant glioma is ongoing[3]. Cash and Assets - As of June 30, 2024, Nuvation Bio reported cash, cash equivalents, and marketable securities totaling 577.2 million[5]. - Cash and cash equivalents decreased from 42,649,000asofDecember31,2023,to42,649,000 as of December 31, 2023, to 34,285,000 as of June 30, 2024, a decline of about 19.7%[11]. - Total current assets decreased from 616,434,000asofDecember31,2023,to616,434,000 as of December 31, 2023, to 587,172,000 as of June 30, 2024, a decline of approximately 4.3%[11]. - Class A convertible preferred stock outstanding as of June 30, 2024, was valued at 274,938,000,with851,202sharesissued[11].WeightedaveragecommonsharesoutstandingforthethreemonthsendedJune30,2024,were244,738,000,comparedto218,848,000forthesameperiodin2023,anincreaseofapproximately11.8274,938,000, with 851,202 shares issued[11]. - Weighted average common shares outstanding for the three months ended June 30, 2024, were 244,738,000, compared to 218,848,000 for the same period in 2023, an increase of approximately 11.8%[12]. Liabilities - Total liabilities increased from 16,362,000 as of December 31, 2023, to 62,665,000asofJune30,2024,anincreaseofapproximately28362,665,000 as of June 30, 2024, an increase of approximately 283%[11]. Regulatory and Product Development - Taletrectinib has been granted Orphan Drug Designation by the U.S. FDA for the treatment of ROS1-positive non-small cell lung cancer (NSCLC)[3]. - The company plans to present pooled data from the pivotal Phase 2 TRUST-I and TRUST-II studies at the ESMO Congress 2024 to support its planned New Drug Application (NDA) in the U.S.[2]. - Nuvation Bio aims to potentially commercialize taletrectinib in the U.S. in 2025, pending regulatory approval[2]. - The company recorded a 425.1 million charge for acquired in-process research and development expenses due to the acquisition of AnHeart Therapeutics[5].