Workflow
Abeona Therapeutics(ABEO) - 2024 Q3 - Quarterly Results

Financial Performance - Abeona Therapeutics reported a net loss of 30.3millionforQ32024,comparedtoanetlossof30.3 million for Q3 2024, compared to a net loss of 11.8 million in Q3 2023, reflecting an increase in losses due to higher expenses[8]. - Abeona's total expenses for Q3 2024 were 15.3million,comparedto15.3 million, compared to 11.3 million in Q3 2023, indicating a significant increase in operational costs[12]. - Research and development expenses for Q3 2024 were 8.9million,upfrom8.9 million, up from 7.1 million in the same period of 2023, while general and administrative expenses rose to 6.4millionfrom6.4 million from 4.2 million[8]. - Total stockholders' equity increased to 45,773millionasofSeptember30,2024,comparedto45,773 million as of September 30, 2024, compared to 14,826 million as of December 31, 2023[15]. - Accumulated deficit rose to (803,965)millionfrom(803,965) million from (749,524) million[15]. - Total liabilities and stockholders' equity reached 120,592million,upfrom120,592 million, up from 64,002 million[15]. - Additional paid-in capital increased to 849,388millionfrom849,388 million from 764,151 million[15]. - Accumulated other comprehensive loss increased to (84)millionfrom(84) million from (66) million[15]. - Total shares issued and outstanding remained at 26,523,878 as of September 30, 2024, unchanged from December 31, 2023[15]. Cash Position - As of September 30, 2024, the company had cash, cash equivalents, short-term investments, and restricted cash totaling 110.0million,downfrom110.0 million, down from 123.0 million as of June 30, 2024[6]. - Abeona's current cash resources are estimated to fund operations into 2026, excluding potential revenue from pz-cel sales[7]. Product Development and Regulatory Progress - The FDA accepted the resubmission of Abeona's Biologics License Application (BLA) for pz-cel, with a target action date set for April 29, 2025[1][4]. - Abeona has made significant progress in commercial readiness for pz-cel, including discussions with payors and onboarding treatment centers[2][4]. - The Centers for Medicare and Medicaid Services (CMS) assigned a product-specific procedure code for pz-cel, facilitating higher reimbursement levels for the therapy[3]. - The company has received new patents related to pz-cel, which are expected to enhance its intellectual property position in the market[3]. Operational Expansion - The company entered a lease agreement for additional manufacturing space in Cleveland, Ohio, to expand its production capacity[3].