Biopharma Transcript

Kymera Therapeutics, Inc. KYMR

Nasdaq · Phase 2 · immunology/inflammation · small molecule · EDGAR · Updated Nov 5, 2026

Kymera Therapeutics, Inc. (Nasdaq: KYMR) is an immunology/inflammation drug developer. Its lead program, KT-621, is in Phase 2 for Atopic Dermatitis and Asthma.

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Pipeline

ProgramIndicationModalityStage
KT-621Moderate to Severe Atopic Dermatitis (AD)small moleculePhase 2
KT-621Moderate to Severe Asthmasmall moleculePhase 2
KT-579Lupussmall moleculePhase 1
KT-485/SAR447971Immunology/inflammation (excluding oncology)small moleculePhase 1
KT-200Undisclosedsmall moleculePre-clinical

Recent results and decisions

  1. Oct 29, 2026
    positive KT-579 Phase 1 healthy volunteer trial demonstrated deep sustained IRF5 degradation (≥90% median degradation), robust modulation of disease-relevant biomarkers, and favorable safety profile comparable to placebo.The positive results from the Phase 1 healthy volunteer trial of KT-579, which we reported today, demonstrate strong translation of its preclinical pharmacology into humans and highlight its potential to modulate multiple core inflammatory pathways. Filing
  2. Oct 29, 2026
    n/a KT-579 LUMORA Phase 1b trial in approximately 30 lupus patients planned to start by early 2027.The KT-579 LUMORA Phase 1b trial in lupus patients is planned to start by early 2027. Filing
  3. Oct 29, 2026
    completed enrollment Last patient completed last visit in KT-621 BROADEN2 Phase 2b atopic dermatitis trial, with topline data to be reported by year-end 2026.In October 2026, the last patient received their final dose and completed the week 16 visit in the KT-621 BROADEN2 Phase 2b clinical trial in patients with moderate to severe AD. Filing

5 more on record.

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