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Kymera' s Q1 Loss Narrower Than Expected, Pipeline Progress Encouraging
KYMRKymera Therapeutics(KYMR) ZACKS· ZACKS·2025-05-09 18:30

Core Insights - Kymera Therapeutics reported a first-quarter 2025 loss of 82 cents per share, which is an improvement compared to the Zacks Consensus Estimate of a loss of 92 cents and a loss of 69 cents per share in the same quarter last year [1][2] - The year-over-year loss increase was attributed to higher research and development (R&D) expenses, which rose by 64.3% to 80.2million[4][5]Collaborationrevenuesreached80.2 million [4][5] - Collaboration revenues reached 22.1 million, exceeding the Zacks Consensus Estimate of 10millionandupfrom10 million and up from 10.3 million in the year-ago quarter [1][2] Financial Performance - R&D expenses increased significantly due to investments in the STAT6 and TYK2 degrader programs, as well as rising occupancy costs related to the growth of the R&D organization [4] - General and administrative expenses rose by 13% year over year to 16.3million,primarilyduetoincreasedlegalandprofessionalservicefees[5]AsofMarch31,2025,Kymerahad16.3 million, primarily due to increased legal and professional service fees [5] - As of March 31, 2025, Kymera had 775 million in cash and cash equivalents, providing a cash runway into the first half of 2028 [5] Pipeline Developments - Kymera completed a phase I study on KT-621, with data expected next month [8] - The company initiated dosing in the KT-621 BroADen phase Ib study for atopic dermatitis patients, with results anticipated in the fourth quarter of 2025 [9] - Plans are in place to begin two parallel phase IIb studies in atopic dermatitis and asthma patients in late 2025 and early 2026, respectively [10] Strategic Decisions - Kymera has named KT-579 as its lead development candidate, with plans to advance it into phase I testing in early 2026 [11] - The company is conducting two phase IIb dose-ranging trials for hidradenitis suppurativa and atopic dermatitis in collaboration with Sanofi, with primary completion expected in 2026 [12] - Kymera has decided not to advance KT-295 into clinical development, allowing a focus on other pipeline programs [13]