Financial Performance - Jasper Therapeutics reported a net loss of 16.6 million in Q4 2023, resulting in a basic and diluted net loss per share of 4.89 for the year, respectively[9]. - Research and development expenses for Q4 2024 were 13.8 million in Q4 2023, while total operating expenses for the year were 68.9 million in 2023[9]. - Jasper's total operating expenses for the year included 20.4 million in general and administrative expenses[9]. - Total current assets decreased from 75,811 million in December 2024, a decline of approximately 14.8%[11]. - Cash and cash equivalents dropped from 71,637 million in December 2024, representing a decrease of about 17.5%[11]. - Total liabilities increased from 18,225 million in December 2024, an increase of approximately 10.7%[11]. - Current liabilities rose from 15,237 million in December 2024, marking an increase of about 23.1%[11]. - Accumulated deficit widened from (240,869) million in December 2024, reflecting a deterioration of approximately 42.0%[11]. - Total stockholders' equity decreased from 61,674 million in December 2024, a decline of about 21.3%[11]. - Additional paid-in capital increased from 302,541 million in December 2024, an increase of approximately 21.9%[11]. - Non-current portion of operating lease liabilities decreased from 724 million in December 2024, a reduction of about 60.0%[11]. - Property and equipment, net declined from 1,875 million in December 2024, a decrease of approximately 31.3%[11]. - Prepaid expenses and other current assets increased from 4,174 million in December 2024, an increase of about 103.5%[11]. Clinical Studies and Developments - The BEACON Phase 1b/2a study showed a more than 25-point improvement in urticaria activity score (UAS7) for multiple dosing regimens of briquilimab at doses ≥120mg[3]. - In the SPOTLIGHT Phase 1b/2a study, 93% of participants achieved a clinical response within six weeks, with 83% of those in the 120mg cohort experiencing a complete response[5]. - Jasper has regulatory clearance to evaluate 240mg Q8W and a 240mg loading dose followed by 180mg Q8W in the BEACON study, with data expected mid-2025 from four cohorts[3]. - The company plans to advance briquilimab into a pivotal Phase 2b study in CSU, expected to commence in the second half of 2025[2]. - Jasper commenced an open-label extension study for chronic urticarias, with initial data from approximately 30 patients expected around mid-2025[5]. - The ETESIAN Phase 1b/2a clinical challenge study for asthma has begun, aiming to enroll approximately 30 patients across seven sites in Canada[5].
Jasper Therapeutics(JSPR) - 2024 Q4 - Annual Results