KYMR · Company research
5 upcoming catalysts · 0 phase 2+ trials on file
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Kymera expects to report results from its Phase 2b (enrollment complete) study of KT-621 (oral STAT6 degrader) for moderate-to-severe atopic dermatitis in Q4 2026 (Oct–Dec) (no exact date yet). This is the first look at whether the drug did what the company hoped.
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Kymera expects to report results from its Phase 1 study of KT-579 (oral IRF5 degrader) for immunology (lupus and other autoimmune diseases) in Q4 2026 (Oct–Dec) (no exact date yet). Phase 1 is an early safety study in a small group of people.
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KT-621 Phase 3 initiation in atopic dermatitis, expected in the first half of 2027 (no exact date yet). A company milestone for Kymera (KT-621 (oral STAT6 degrader) for moderate-to-severe atopic dermatitis): a step in the program rather than a decision or a data readout.
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Gilead IND filing for KT-200 CDK2 degrader, expected during 2027 (no exact date yet). A company milestone for Kymera (KT-200 for oncology (CDK2)): a step in the program rather than a decision or a data readout.
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Kymera expects to report results from its Phase 2b study of KT-621 (oral STAT6 degrader) for asthma in the second half of 2027 (no exact date yet). This is the first look at whether the drug did what the company hoped.
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BROADEN2 enrollment done early; KT-621 topline pulled forward to YE2026, on Jun 25, 2026. A company milestone for Kymera (KT-621 for moderate-to-severe atopic dermatitis): a step in the program rather than a decision or a data readout.
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