Financial Performance - Prelude Therapeutics reported a net loss of 0.46 per share, for Q2 2024, compared to a net loss of 0.54 per share, in the same period last year[12]. - Total operating expenses for Q2 2024 were 32.4 million in the prior year period[16]. - Accumulated deficit increased significantly from 522,561,000, reflecting a rise of about 14.5%[19]. - Total stockholders' equity decreased from 182,276,000, a decline of approximately 23.1%[19]. Research and Development - Research and Development (R&D) expenses increased to 25.0 million in the prior year period, primarily due to increased chemistry, manufacturing, and controls (CMC) expenses[10]. - The interim Phase 1 data for PRT3789, a first-in-class SMARCA2 degrader, is scheduled for oral presentation at the ESMO Congress on September 13, 2024[6]. - Prelude has received IND authorization for PRT7732, its first-in-class oral SMARCA2 degrader, which is expected to enter Phase 1 clinical development in the second half of 2024[8]. - PRT2527, a selective CDK9 inhibitor, is on track to present interim Phase 1 data in Q4 2024, with ongoing dose escalation in both lymphoid and myeloid malignancies[9]. - The company is collaborating with Merck to evaluate PRT3789 in combination with KEYTRUDA® in patients with SMARCA4-mutated cancers, with a Phase 2 trial anticipated to start in Q4 2024[7]. - The company is advancing its clinical programs with a focus on the SMARCA pathway, aiming to address high unmet medical needs in cancer treatment[2]. Cash and Assets - As of June 30, 2024, the company had 235,589,000 on December 31, 2023, to 25,291,000 to 207,644,000 to 40,575,000 to 4,580,000 to 15,768,000 to 693,252,000 to 30,412,000 to $29,574,000, a reduction of about 2.8%[18]. Educational Initiatives - Prelude has launched an educational video series on SMARCA biology and the development of SMARCA2 degraders, available on its website[5].
Prelude Therapeutics(PRLD) - 2024 Q2 - Quarterly Results