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Prelude Therapeutics(PRLD) - 2024 Q3 - Quarterly Results

Financial Performance - Prelude Therapeutics reported a net loss of 32.3million,or32.3 million, or 0.43 per share, for Q3 2024, compared to a net loss of 30.6million,or30.6 million, or 0.45 per share, in the same period last year[14]. - General and administrative expenses rose to 7.9millioninQ32024from7.9 million in Q3 2024 from 7.1 million in Q3 2023, mainly due to increased professional fees[13]. - Accumulated deficit increased from (456,390,000)to(456,390,000) to (554,832,000), indicating a worsening financial position[20]. Research and Development - Research and development expenses increased to 29.5millioninQ32024from29.5 million in Q3 2024 from 26.3 million in Q3 2023, primarily due to higher chemistry, manufacturing, and controls costs[12]. - PRT3789, a first-in-class intravenous SMARCA2 degrader, is in Phase 1 clinical development, with enrollment on track and monotherapy dose escalation expected to conclude by year-end 2024[4]. - Interim data from the PRT3789 trial showed partial responses in 4 out of 26 evaluable patients with advanced NSCLC or esophageal cancers[4]. - The company initiated a Phase 1 trial for PRT7732, an oral SMARCA2 degrader, with patient enrollment currently ongoing[6]. - Prelude presented preclinical data from its Precision ADC platform, demonstrating potent activity of SMARCA2/4 degrader payloads conjugated to various antibodies[8]. - PRT2527, a CDK9 inhibitor, is advancing in clinical trials, with interim data to be presented at the American Society of Hematology Annual Meeting in December 2024[10]. Financial Position - The company has 153.6millionincash,cashequivalents,andmarketablesecuritiesasofSeptember30,2024,whichisexpectedtofundoperationsinto2026[11].Totalcurrentassetsdecreasedfrom153.6 million in cash, cash equivalents, and marketable securities as of September 30, 2024, which is expected to fund operations into 2026[11]. - Total current assets decreased from 235,589,000 on December 31, 2023, to 156,387,000onSeptember30,2024,adeclineofapproximately33.5156,387,000 on September 30, 2024, a decline of approximately 33.5%[19]. - Cash and cash equivalents dropped from 25,291,000 to 11,134,000,representingadecreaseofabout56.011,134,000, representing a decrease of about 56.0%[19]. - Marketable securities decreased from 207,644,000 to 142,492,000,areductionofapproximately31.4142,492,000, a reduction of approximately 31.4%[19]. - Total stockholders' equity fell from 237,090,000 to 156,431,000,adeclineofaround33.9156,431,000, a decline of around 33.9%[20]. - Total liabilities remained relatively stable, increasing slightly from 40,575,000 to 40,789,000[19].Accountspayablerosefrom40,789,000[19]. - Accounts payable rose from 4,580,000 to 5,921,000,anincreaseofapproximately29.35,921,000, an increase of approximately 29.3%[19]. - Accrued expenses and other current liabilities decreased from 15,768,000 to 13,579,000,adeclineofabout13.913,579,000, a decline of about 13.9%[19]. - The company reported 42,178,012 shares issued and outstanding as of September 30, 2024, compared to 42,063,995 shares on December 31, 2023[19]. - Additional paid-in capital increased from 693,252,000 to $711,091,000, reflecting a growth of approximately 2.6%[20]. Collaborations - The company has entered into a collaboration agreement with Pfizer Ignite to support its SMARCA2 degrader development programs while retaining full ownership of its programs[7].