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Spyre Therapeutics Reports Fourth Quarter and Full Year 2024 Financial Results and Provides Corporate Update
SYRESpyre Therapeutics(SYRE) Prnewswire·2025-02-27 21:05

Core Insights - Spyre Therapeutics reported positive interim pharmacokinetic and safety data for SPY001 in a Phase 1 trial and raised 230millionthroughapublicofferingtostrengthenitsbalancesheet[1][12]Thecompanyisontrackformultiplemilestones,includinginterimPhase1datareadoutsforSPY002andSPY003expectedin2025,andtheinitiationofaPhase2trialforSPY001inulcerativecolitisplannedformid2025[1][2]ThecompanyaimstoexpandSPY002intorheumatoidarthritiswithaPhase2trialinitiationalsoexpectedinmid2025[1][11]FinancialOverviewAsofDecember31,2024,thecompanyhadcash,cashequivalents,andmarketablesecuritiestotaling230 million through a public offering to strengthen its balance sheet [1][12] - The company is on track for multiple milestones, including interim Phase 1 data readouts for SPY002 and SPY003 expected in 2025, and the initiation of a Phase 2 trial for SPY001 in ulcerative colitis planned for mid-2025 [1][2] - The company aims to expand SPY002 into rheumatoid arthritis with a Phase 2 trial initiation also expected in mid-2025 [1][11] Financial Overview - As of December 31, 2024, the company had cash, cash equivalents, and marketable securities totaling 603 million, providing a financial runway into the second half of 2028 [1][12] - Research and development expenses for Q4 2024 were 50.5million,anincreasefrom50.5 million, an increase from 33.7 million in Q4 2023, driven by clinical development and manufacturing costs [13] - General and administrative expenses decreased to 10.8millioninQ42024from10.8 million in Q4 2024 from 14.1 million in Q4 2023, attributed to higher stock compensation expenses in the previous year [14] Development Pipeline - The company has four programs in development, with three targeting inflammatory bowel disease (IBD) and one undisclosed target [4] - SPY001 is a monoclonal antibody targeting α4β7, showing a favorable safety profile and a half-life greater than 90 days, supporting potential Q6M maintenance dosing [5][6] - SPY002 and SPY003 are also being developed with half-life extension technology, aiming for infrequent subcutaneous maintenance dosing [6][7] Recent Corporate Updates - The company initiated first-in-human trials for SPY002 in December 2024, with interim data expected in Q2 2025 [11] - SPY003 is on track to begin its first-in-human trial in Q1 2025, with interim data anticipated in the second half of 2025 [11] - Spyre was added to the Nasdaq Biotechnology Index in December 2024, reflecting its growing presence in the biotech sector [11]