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Aptose Biosciences(APTO) - 2023 Q4 - Annual Results
APTOAptose Biosciences(APTO)2024-03-26 20:04

Financial Performance - Aptose reported a net loss of 51.2millionfortheyearendedDecember31,2023,anincreaseof51.2 million for the year ended December 31, 2023, an increase of 9.4 million compared to a net loss of 41.8millionin2022[12].Cashandcashequivalentsdecreasedto41.8 million in 2022[12]. - Cash and cash equivalents decreased to 9.3 million as of December 31, 2023, down from 47.0millionattheendof2022[10].Totalshareholdersequitydecreasedto47.0 million at the end of 2022[10]. - Total shareholders' equity decreased to (2.9) million as of December 31, 2023, compared to 37.7millionin2022[10].ResearchandDevelopmentResearchanddevelopmentexpensesroseto37.7 million in 2022[10]. Research and Development - Research and development expenses rose to 36.8 million in 2023, up 8.7millionfrom8.7 million from 28.1 million in 2022, primarily due to increased costs associated with the tuspetinib program[14]. - Tuspetinib achieved a complete response/complete response with partial hematologic recovery (CR/CRh) rate of 36% among patients naive to venetoclax at the recommended Phase 2 dose of 80 mg[5]. - The G3 formulation of luxeptinib demonstrated approximately 10-fold better absorption compared to the original G1 formulation, achieving desired plasma exposure levels[7]. - The company plans to initiate a pilot triplet study of tuspetinib, venetoclax, and a hypomethylating agent in frontline therapy for newly diagnosed AML patients in Summer 2024[8]. Capital and Funding - The company completed a public offering on January 30, 2024, raising approximately 9.7millionfromthesaleof5,649,122commonsharesat9.7 million from the sale of 5,649,122 common shares at 1.71 per share[3]. - A private placement with Hanmi Pharmaceutical on January 31, 2024, generated 4million,withsharessoldat4 million, with shares sold at 1.90 each, an 11% premium over the public offering price[4]. Risks and Uncertainties - The company acknowledges significant risks and uncertainties that could impact future results, including capital acquisition for research and operations[23]. - Early-stage drug development risks include demonstrating efficacy, development time/cost, and regulatory approval processes[23]. - There is a potential risk of new manufacturers failing to produce acceptable GMP batches in sufficient quantities[23]. - Unexpected manufacturing defects are highlighted as a significant risk factor[23]. - The company does not intend to update forward-looking statements unless required by law, indicating a cautious approach to investor communications[24]. - Investors are advised not to overly rely on forward-looking statements due to inherent uncertainties[24]. Administrative Expenses - General and administrative expenses increased to 15.6millionin2023,upfrom15.6 million in 2023, up from 14.5 million in 2022, driven by higher salaries and professional fees[17].