Kymera Therapeutics, Inc. · Healthcare · Biotechnology
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Mkt cap
$9.38B
P/E ratio
-32.36
FY Revenue
$51.48M
EPS
-3.58
Gross Margin
100.00%
Sector
Healthcare
AI report sections
BULLISH
KYMR
Kymera Therapeutics, Inc.
No AI report section text found yet for this symbol.
Kymera's CEO Sold $6 Million in Stock After a 170% Run
Kymera Therapeutics CEO Nello Mainolfi sold 50,000 shares for $6 million on July 7, 2026, following a 170% stock surge over 12 months. The sale involved exercising options at $2.08 and selling at $119 per share under a pre-scheduled Rule 10b5-1 trading plan. Despite the sale, Mainolfi retains 666,568 shares worth $79.5 million and 90,000 options, indicating continued confidence in the company's pipeline, particularly KT-621 in Phase 2b trials with FDA Fast Track status.
The CEO's sale is characterized as a non-event and routine option exercise rather than a sign of concern. The insider maintains substantial equity holdings ($79.5M in shares plus options), indicating confidence in the company. The article emphasizes upcoming 2027 clinical trial readouts as the real catalysts, with adequate cash runway ($1.55B) through 2029. The sale appears to be profit-taking after significant gains rather than a bearish signal.
PositiveGlobeNewswire Inc.• Na
Kymera Therapeutics Presents Phase 1 Data in Healthy Japanese Adults for KT-621, a First-in-Class Oral STAT6 Degrader, at the Japanese Dermatological Association Annual Meeting
Kymera Therapeutics announced Phase 1 results for KT-621, a first-in-class oral STAT6 degrader, in healthy Japanese adults at the Japanese Dermatological Association Annual Meeting. The data showed consistent safety and pharmacokinetic/pharmacodynamic profiles with previous studies, demonstrating rapid and sustained STAT6 degradation (≥98% at Day 7). The company has parallel Phase 2b trials ongoing in atopic dermatitis (BROADEN2) and asthma (BREADTH), with data expected by mid-2027 and late 2027, respectively.
KYMRSTAT6 degraderKT-621Phase 1 trialatopic dermatitisasthmaType 2 inflammationtargeted protein degradation
Sentiment note
The company reported consistent and favorable Phase 1 data across different populations (Japanese and non-Japanese adults), demonstrating robust STAT6 degradation, good safety profile, and clinical efficacy. Advancement of parallel Phase 2b trials in multiple indications and achievement of regulatory milestones support positive momentum in drug development pipeline.
PositiveGlobeNewswire Inc.• Kymera Therapeutics
Kymera Therapeutics Presents New Preclinical Lupus Data for KT-579, First-in-Class, Oral IRF5 Degrader, at EULAR and FOCIS Congresses
Kymera Therapeutics announced preclinical data for KT-579, an oral IRF5 degrader, demonstrating disease-modifying activity in lupus models comparable or superior to approved therapies. The compound showed consistent activity across multiple disease pathways including Type I interferons and pro-inflammatory cytokines. Phase 1 healthy volunteer trial is ongoing with data expected in the second half of 2026, followed by a planned patient proof-of-concept trial in lupus.
KYMRKT-579IRF5 degraderlupuspreclinical dataautoimmune diseasePhase 1 trialtargeted protein degradation
Sentiment note
Company presented promising preclinical data showing KT-579 demonstrates disease-modifying activity comparable or superior to approved therapies across multiple lupus models. The drug candidate shows broad activity across multiple disease-driving pathways with no adverse effects observed in preclinical safety studies. Phase 1 trial is progressing on schedule with data expected in 2H26, supporting advancement toward clinical proof-of-concept.
PositiveGlobeNewswire Inc.• Na
Kymera Therapeutics Announces Presentations on KT-621, a First-In-Class, Oral STAT6 Degrader, at the Society for Investigative Dermatology and American Thoracic Society Congresses
Kymera Therapeutics announced presentations of Phase 1b clinical data for KT-621, its first-in-class oral STAT6 degrader, at the Society for Investigative Dermatology and American Thoracic Society congresses. The data demonstrated deep STAT6 degradation in blood and skin, reductions in Type 2 inflammatory biomarkers, and favorable safety profile. Parallel Phase 2b trials in atopic dermatitis and asthma are ongoing with data expected by mid-2027 and late 2027, respectively.
KYMRKT-621STAT6 degraderatopic dermatitisasthmaPhase 1b clinical trialType 2 inflammationtargeted protein degradation
Sentiment note
The company reported encouraging Phase 1b clinical data for its lead candidate KT-621, demonstrating robust target engagement, meaningful biomarker reductions, clinical efficacy improvements, and favorable safety profile. Advancement to parallel Phase 2b trials in multiple indications and potential to address 140+ million patients with Type 2 inflammatory diseases supports positive outlook.
PositiveGlobeNewswire Inc.• Not Specified
Kymera Therapeutics to Participate in Upcoming May Investor Conferences
Kymera Therapeutics announced participation in upcoming investor conferences in May 2026 and presented preclinical data for KT-579, its first-in-class oral IRF5 degrader for inflammatory bowel disease, showing activity comparable or superior to approved therapies. The company has Phase 1 data expected in H2 2026 and ongoing Phase 2b trials for KT-621 with results anticipated by mid-to-late 2027.
KYMRtargeted protein degradationoral small molecule degraderKT-579IRF5 degraderinflammatory bowel diseaseKT-621STAT6
Sentiment note
The company demonstrated promising preclinical efficacy data for KT-579 showing activity comparable or superior to approved therapies, has ongoing Phase 1 and Phase 2b trials with near-term data expectations, and received FDA Fast Track designation, indicating clinical progress and regulatory support for its pipeline.
PositiveGlobeNewswire Inc.• Na
Kymera Therapeutics to Report First Quarter 2026 Financial Results on April 30, 2026
Kymera Therapeutics will report Q1 2026 financial results on April 30, 2026. The company announced FDA Fast Track designation for KT-621, a first-in-class oral STAT6 degrader for moderate to severe asthma, with Phase 2b trial data expected in late 2027. Additionally, Gilead Sciences exercised its option to license KT-200, triggering a $45 million milestone payment to Kymera.
GILDKYMRtargeted protein degradationKT-621STAT6 degraderasthmaFDA Fast TrackKT-200
Sentiment note
Company received FDA Fast Track designation for lead candidate KT-621, indicating regulatory support and accelerated development pathway. Additionally, Gilead's option exercise on KT-200 with a $45 million milestone payment demonstrates validation of Kymera's technology platform and provides significant funding.
NeutralThe Motley Fool• Jonathan Ponciano
Protagonist Stock Up 120%, but One Fund Just Revealed a $170 Million Exit
Hedge fund BVF fully exited its position in Protagonist Therapeutics (PTGX), selling 2.56 million shares worth $170.12 million. Despite the stock rallying 120% over the past year, the fund's exit reflects a disciplined capital rotation strategy following the company's New Drug Application submission for rusfertide in polycythemia vera, marking a shift from clinical-stage risk to regulatory execution risk.
PTGXKYMRRVMDRVMDWbiotech exithedge fund liquidationProtagonist TherapeuticsNDA submission
Sentiment note
Listed as BVF's top holding post-exit ($428.17M, 14.4% of AUM), indicating continued confidence, but no specific news or developments mentioned in the article.
PositiveThe Motley Fool• Jonathan Ponciano
Disc Medicine Stock Is Swinging, but This Fund's New $52 Million Bet Shows Conviction
Hedge fund BVF invested $52 million in Disc Medicine (IRON) by acquiring 650,000 shares in Q4, demonstrating conviction in the clinical-stage biotech company despite recent FDA setbacks. The investment was made before the FDA's Complete Response Letter in February and a subsequent 20% stock decline. With $791 million in cash runway through 2029, Disc Medicine's investment thesis now hinges on Phase 3 APOLLO trial data expected in Q4 and a potential FDA decision by mid-2027.
Listed as BVF's top holding at $428.2M (14.4% of AUM), indicating strong conviction and confidence in this biotech platform as a differentiated investment with binary catalysts.
PositiveGlobeNewswire Inc.• Kymera Therapeutics
Kymera Therapeutics Outlines Key 2026 Objectives and Strategy to Advance Industry Leading Portfolio of Oral Immunology Programs
Kymera Therapeutics announced its 2026 clinical and preclinical milestones, including ongoing Phase 2b trials for KT-621 in atopic dermatitis and asthma with data expected in 2027, initiation of Phase 1 testing for KT-579 in Q1 2026, and advancement of at least one new development candidate toward IND. The company maintains $1.6 billion in cash with runway into 2029.
Company announced strong 2026 objectives with multiple clinical milestones, positive Phase 1b data for KT-621 showing efficacy comparable to dupilumab, FDA Fast Track designation, robust cash position of $1.6 billion with runway into 2029, and expansion of pipeline with new development candidates. Successful execution of strategy and clinical progress support positive outlook.
PositiveInvesting.com• Leo Miller
Insider Buying: Smart Money Just Spent +$100M on These 3 Stocks
Three stocks have attracted over $100 million in insider buying from prominent institutional investors: DoorDash (Sequoia Capital), Kenvue (Starboard Value LP), and Kymera Therapeutics (Baker Bros. Advisors). While these purchases signal confidence from sophisticated capital, investors should consider offsetting insider sales and the long-term viability of these bets.
Baker Bros. Advisors purchased $172.5 million in shares, increasing its position by 30% following positive Phase 1b trial results for KT-621. This represents strong institutional confidence, though the drug remains early-stage and offsetting insider sales of $21.6 million provide some counterbalance.
PositiveBenzinga• Globe Newswire
Kymera Therapeutics Announces Closing of Upsized $602 Million Public Offering and Full Exercise of Underwriters' Option to Purchase Additional Shares
Kymera Therapeutics successfully closed a public offering of $602 million, selling 8,050,000 shares at $86.00 per share, including the full exercise of underwriters' option to purchase additional shares.
KYMRMSMSPAMSPEpublic offeringbiotechnologytargeted protein degradationsmall molecule degraders
Sentiment note
Successfully raised substantial capital ($692.3 million gross proceeds) through an upsized public offering, indicating strong investor confidence in the company's potential and clinical-stage biotechnology pipeline
PositiveGlobeNewswire Inc.• Justine Koenigsberg
Kymera Therapeutics Announces Pricing of Upsized $602 Million Public Offering
Kymera Therapeutics plans to raise $602 million through a public offering of 7 million common stock shares at $86 per share, with proceeds intended to advance its preclinical and clinical degrader programs.
KYMRMSMSPAMSPEpublic offeringsmall molecule degraderbiopharmaceuticalstock sale
Sentiment note
Company is raising significant capital ($602 million) to fund pipeline development, indicating strong financial strategy and investor confidence
News and sentiment labels describe article tone and are provided for research purposes only. They are not trading recommendations or forecasts.
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