Spyre Therapeutics reported a net loss of $38.8 million for the second quarter of 2024. The company's cash and cash equivalents, marketable securities, and restricted cash totaled $426.3 million as of June 30, 2024. Dosing was initiated in the Phase 1 trial of SPY001, with interim proof-of-concept data expected by year-end 2024.
Initiated dosing in Phase 1 trial of SPY001.
SPY002 remains on track to begin first-in-human trials in the second half of 2024.
Nominated a development candidate for SPY003, with expectations to begin a first-in-human trial in the first half of 2025.
$426 million of cash, cash equivalents, marketable securities, and restricted cash as of June 30, 2024, with expected runway well into 2027.
Spyre expects to have reported Phase 1 data from their α4β7 and TL1A programs and have an ongoing Phase 1 trial of their IL-23 program reporting data shortly thereafter.