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Kymera reports Q1 2026 results, advances KT-621 and KT-579 trials, and gains $45M milestone from Gilead licensing KT-200.

Company Fundamentals
30 Apr 2026
GlobeNewsWire
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Bullish
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Kymera Therapeutics announced its Q1 2026 financial results, highlighting ongoing Phase 2b trials for KT-621 in atopic dermatitis and asthma with data expected by mid and late 2027. The FDA granted Fast Track status to KT-621 for moderate to severe asthma. KT-579 is in Phase 1 trials with data expected in the second half of 2026. Gilead Sciences licensed KT-200, triggering a $45 million milestone payment, with IND planned in 2027. Kymera holds $1.55 billion in cash, supporting operations into 2029 and continues to advance its pipeline with a focus on oral small molecule degraders for immunological diseases.

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