Kymera Therapeutics, Inc. (KYMR) Stock Analysis
Breakout setup
Healthcare · Biotechnology
Sell if holding. Engine safety override at $87.44: Quality below floor (1.6 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.8/10 and A.R:R 1.5:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 16%; Elevated put/call ratio: 2.30; Below-average business quality.
Kymera Therapeutics is a clinical-stage biopharmaceutical company developing oral targeted protein degraders for immune-inflammatory diseases, with lead programs KT-621 (STAT6, Phase 2b in atopic dermatitis and asthma) and KT-579 (IRF5, Phase 1). Revenue comes from collaboration... Read more
Sell if holding. Engine safety override at $87.44: Quality below floor (1.6 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.8/10 and A.R:R 1.5:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 16%; Elevated put/call ratio: 2.30; Below-average business quality. Chart setup: Golden cross, above all MAs, RSI 60, MACD bullish. Score 5.8/10, moderate confidence.
Passes 6/7 gates (positive momentum, favorable risk/reward ratio, clean insider activity, earnings proximity 55d clear, semi cycle peak clear, materials cycle peak clear). Suitability: aggressive.
About Kymera Therapeutics, Inc.
About Kymera Therapeutics, Inc.
Kymera Therapeutics has advanced its lead STAT6 degrader, KT-621, into two concurrent Phase 2b clinical trials—BROADEN2 in atopic dermatitis and BREADTH in asthma—with data expected by mid-2027 and late-2027, respectively. The company held $1,619.4 million in cash and marketable securities at December 31, 2025, supporting operations through a projected 2029 runway, against an accumulated deficit of $1,066.0 million. KT-579 (IRF5) began Phase 1 testing in healthy volunteers during 2025, and Sanofi plans to advance KT-485/SAR447971 (IRAK4) into clinical testing in 2026.
Kymera generates collaboration revenue rather than product sales. The Sanofi partnership covers IRAK4 degraders outside oncology and immuno-oncology; in June 2025, Sanofi exercised its participation election for KT-485/SAR447971, which it intends to advance clinically in 2026. A separate June 2025 agreement with Gilead Sciences targets CDK2 molecular glue degraders. The company's discovery platform applies targeted protein degradation, a modality that recruits the body's natural ubiquitin-proteasome machinery to eliminate disease-causing proteins—enabling it to target historically undrugged transcription factors such as STAT6 and IRF5. Drug manufacturing is outsourced to contract manufacturers, which the filing identifies as a critical dependency for clinical supply. Net losses were $311.4 million in 2025, $223.9 million in 2024, and $147.0 million in 2023, driven entirely by research, development, and general and administrative costs.
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The company's clinical valuation rests heavily on KT-621's Phase 2b data readouts. The 10-K acknowledges that "no product candidate using a heterobifunctional degrader has been approved in the United States or Europe," marking the BROADEN2 and BREADTH trials as binary inflection points for the entire TPD platform thesis. Prior discontinuations—KT-295 (TYK2) in May 2025 and Sanofi's decision to abandon first-generation KT-474 in favor of KT-485 in June 2025—demonstrate that late-stage clinical redirection is possible and can impair program-level investment value.
See also: Healthcare · Biotechnology
From Kymera Therapeutics, Inc.'s most recent 10-K filing, extracted June 11, 2026.
Recent developments
updated 2026-06-17Recent Developments — Kymera Therapeutics, Inc.
Material events (past 30 days)
- 8K Jun 8, 2026 MEDIUM Item 5.02: COO Jeremy Chadwick resigned effective June 5, 2026, citing personal reasons; no disagreement with company practices cited. Chadwick will remain as employee/advisor until November 2026. No successor named.
Latest news
- NEWS Kymera Therapeutics Announces Results From Its Phase 1 Study Of KT-621 In Healthy Japanese Adults Were Shared At The Jap — benzinga Jun 12, 2026 positive
- NEWS Kymera Therapeutics Announces First Participant Dosed In First-In-Human Phase 1 Clinical Trial Evaluating KT-485, Oral, — benzinga Jun 9, 2026 positive
- NEWS Kymera Therapeutics Presents New Preclinical Data For KT-579, Selective, Oral IRF5 Degrader, Demonstrating Disease-Modif — benzinga Jun 8, 2026 positive
- NEWS Kymera Therapeutics Announces Presentations On Results From KT-621 Clinical Trial At Annual Meetings May 13-16 — benzinga May 15, 2026 positive
- NEWS Canaccord Genuity Initiates Coverage On Kymera Therapeutics with Buy Rating, Announces Price Target of $106 — benzinga May 6, 2026 positive
Generated 2026-06-17T10:41:47Z.
Upcoming dated catalysts
Thesis
Key Metrics
Quality Signals
Options Flow
Concentration Risks(10-K Item 1A)
- MEDIUMpipelinelead programs10-K Item 1A: 'We depend heavily on the successful development of our lead programs.'
Material Events(8-K, last 90d)
- 2026-06-08Item 5.02MEDIUMCOO Jeremy Chadwick resigned effective June 5, 2026, citing personal reasons; no disagreement with company practices cited. Chadwick will remain as employee/advisor until November 2026. No successor named.SEC filing →
Model-generated analysis — not investment advice. Not a registered investment advisor. Past performance does not guarantee future results.
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Rating Breakdown
4 floor-breakers·1 ceiling hit
Risk profile below the gate floor. Component breakdown shows what dragged the score down.static
Quality below the gate floor. Component breakdown shows what dragged the score down.static
Technicals below the gate floor. Component breakdown shows what dragged the score down.static
No near-term catalyst priced in. Thesis progression will come from fundamentals grinding, not event reaction.static
Price Targets
Position Sizing
Risk Alerts
Earnings
Verdict History
Frequently Asked Questions
Sell if holding. Engine safety override at $87.44: Quality below floor (1.6 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.8/10 and A.R:R 1.5:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 16%; Elevated put/call ratio: 2.30; Below-average business quality. Chart setup: Golden cross, above all MAs, RSI 60, MACD bullish. Prior stop was $81.32. Score 5.8/10, moderate confidence.
Take-profit target: $107.49 (+22.9% upside). Prior stop was $81.32. Stop-loss: $81.32.
Quality below floor (1.6 < 4.0).
Kymera Therapeutics, Inc. trades at a P/E of N/A (forward -19.7). TrendMatrix value score: 7.5/10. Verdict: Sell.
30 analysts cover KYMR with a consensus score of 4.3/5. Average price target: $119.
What does Kymera Therapeutics, Inc. do?Kymera Therapeutics is a clinical-stage biopharmaceutical company developing oral targeted protein degraders for...
Kymera Therapeutics is a clinical-stage biopharmaceutical company developing oral targeted protein degraders for immune-inflammatory diseases, with lead programs KT-621 (STAT6, Phase 2b in atopic dermatitis and asthma) and KT-579 (IRF5, Phase 1). Revenue comes from collaboration agreements with Sanofi and Gilead rather than product sales; the company held $1.6 billion in cash as of December 31, 2025. It has never generated product revenue.