Core Insights - Kymera Therapeutics reported positive Phase 1 data for KT-621, a once-daily oral STAT6 degrader, which exceeded the company's target product profile and demonstrated a safety profile similar to placebo [1][2][3] - The company is on track to report data from the KT-621 BroADen Phase 1b trial in moderate to severe atopic dermatitis (AD) patients in Q4 2025, with Phase 2b trials in AD and asthma set to begin in Q4 2025 and Q1 2026, respectively [1][2][7] - Kymera has entered a strategic partnership with Gilead to develop CDK2 degraders, with potential total payments of up to $750 million [1][9] - As of July 31, 2025, the company had $1 billion in cash, providing a runway into the second half of 2028 [1][10] Business Highlights - KT-621 demonstrated over 90% mean STAT6 degradation at doses above 1.5 mg, with complete degradation at doses ≥50 mg [3][4] - The drug showed median reductions in Th2 biomarkers, with TARC reduction up to 37% and Eotaxin-3 reduction up to 63% [4] - KT-579, an oral IRF5 degrader, is expected to enter Phase 1 clinical trials in early 2026, showing promise in treating lupus and rheumatoid arthritis [5][8] Collaboration Updates - The partnership with Gilead includes an exclusive option and license agreement for the CDK2 program, with Kymera leading research activities [6][9] - Sanofi plans to advance KT-485, a second-generation IRAK4 degrader, into clinical studies, while Kymera achieved a $20 million milestone related to KT-485 [9] Financial Results - Collaboration revenues for Q2 2025 were $11.5 million, down from $25.7 million in Q2 2024, primarily due to the recognition of deferred revenue from the Sanofi collaboration [11] - Research and development expenses increased to $78.4 million in Q2 2025 from $59.2 million in Q2 2024, driven by investments in the STAT6 program [12] - The net loss for Q2 2025 was $76.6 million, compared to $42.1 million in Q2 2024 [14]

WATERTOWN, Mass., Aug. 04, 2025 (GLOBE NEWSWIRE) -- Kymera Therapeutics, Inc. (NASDAQ: KYMR), a clinical-stage biopharmaceutical company advancing a new class of oral small molecule degrader medicines for immunological diseases, will report second quarter 2025 financial results on August 11, 2025. The Company will host a video conference call and webcast at 8:30 a.m. ET that day. Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines ...

Core Insights - Kymera's shares have surged 70.7% over the past three months, significantly outperforming the industry gain of 9.7% and the broader S&P 500 index [1][9] - The company is focused on targeted protein degradation (TPD) to develop drugs for various immunological diseases [1] Collaboration with Gilead - Kymera has entered an exclusive option and license agreement with Gilead Sciences to advance a novel molecular glue degrader (MGD) program targeting cyclin-dependent kinase 2 (CDK2), which has potential applications in oncology [4][5] - Under the agreement, Kymera will receive an upfront payment of $85 million, with total potential payments reaching up to $750 million [6] - Kymera may also earn tiered royalties on net product sales, while it will lead research activities for the CDK2 program [7] Setback with Sanofi - Kymera faced a setback with Sanofi, which decided to prioritize the development of a different candidate, KT-485, over Kymera's KT-474, impacting potential milestone payments [10][14] - Despite this, Kymera achieved a $20 million milestone related to preclinical activities for KT-485, which is expected to enter early-stage testing next year [12][13] Pipeline Developments - Kymera's pipeline includes ongoing studies for KT-621 in atopic dermatitis and plans for two phase IIb studies in asthma and atopic dermatitis in late 2025 and early 2026 [15] - The company has identified KT-579 as its lead development candidate, with plans to advance it into phase I testing in early 2026 [16]

Company Strategy & Vision - Kymera is developing oral therapies with biologics-like profiles by combining the "right target" with Targeted Protein Degradation (TPD), aiming to expand patient access globally[12] - The company's vision is to reinvent disease treatment as a fully integrated commercial global biotech, supported by $775 million in cash and equivalents, providing a runway into the first half of 2028[20] - Kymera has delivered 5 new investigational degrader drugs into the clinic since 2020, and is on track to deliver a total of 10 by 2026[17] Immunology Market & TPD - The immunology market is large and underserved, with approximately 160 million total patients across key immunologic diseases[26] - Only ~5 million patients (3%) are on systemic advanced therapies, representing >$100 billion in annual sales for key I/I indications, with 2/3 of these therapies being injectable biologics[27] - Targeted Protein Degradation (TPD) can unlock the undrugged proteome, addressing the 80% of disease-causing proteins currently out of reach for existing technologies[22][23] - In industry surveys, 75% of patients would switch from injectable biologics to oral medications with a similar profile[34] Pipeline Programs & Milestones - **STAT6 (KT-621):** Phase 1 Healthy Volunteer (HV) data is expected in June 2025, with Phase 1b Atopic Dermatitis (AD) patient data anticipated in Q4 2025; Phase 2b trials in AD are expected to start in Q4 2025 and in Asthma in Q1 2026[52][83] - The total potential patient impact for STAT6 (KT-621) is >130 million patients, with only ~1% having access to advanced systemic therapies; the market is projected to reach $23B+ with new indications/entrants[83] - **IRF5 (KT-579):** IND-enabling studies are ongoing, with a Phase 1 trial start expected in early 2026[90][175] - In mouse models of lupus, KT-579, dosed once a day for 63 days, leading to 85% and >90% IRF5 degradation, reduced proteinuria (key disease marker) and prevented disease associated mortality better than all other approved or clinically active agents tested[164]

Company Overview - Kymera is a science-driven clinical stage organization focused on developing oral drugs with biologics-like efficacy in immunology[6] - The company has raised $1.7 billion to date, with $850 million in cash on hand, providing a runway to mid-2027[11] - Kymera has delivered 5 new investigational degrader drugs into the clinic since 2020 and is on track to deliver a total of 10 by 2026[14] Targeted Protein Degradation (TPD) Technology - TPD is a small molecule-based modality with gene silencing power that can unlock the undrugged proteome[23, 22] - TPD has been validated across multiple FDA-approved drugs with >$17 billion in combined peak WW sales[23] - Kymera utilizes comprehensive proprietary technologies to identify novel ligands to undrugged proteins, leading to >8 development candidates, including >4 targeting undrugged transcription factors[39, 41] Immunology Market and Oral Degraders - The immunology market has ~160 million total patients across key immunologic diseases[24] - Approximately 5 million patients (3% of total diagnosed) are on systemic advanced therapies with >$100 billion in annual sales for key I/I indications[28] - In multiple surveys, 75% of patients would switch from injectable biologics to oral with similar profile[31] Pipeline and Clinical Development - KT-474 (IRAK4 degrader) has shown >95% IRAK4 degradation in humans[68] with Phase 2b trials in HS and AD ongoing, with completion expected in 1H 2026 (HS) and mid-2026 (AD)[69] - KT-295 (TYK2 degrader) is undergoing IND-enabling studies with Phase 1 healthy volunteer start planned for 2Q 2025[57] - KT-621 (STAT6 degrader) is in Phase 1 trial with recruitment ongoing and multiple SAD/MAD cohorts completed[92] - Kymera aims to build a STAT6 franchise to serve >130 million diagnosed mild and moderate/severe patients with Th2 inflammation[85]

Core Viewpoint - Kymera Therapeutics, Inc. has announced a public offering of $250.8 million in common stock and pre-funded warrants to advance its pipeline of oral small molecule degrader medicines for immunological diseases [1][2]. Group 1: Offering Details - Kymera is selling 5,044,500 shares of common stock at a price of $44.00 per share and pre-funded warrants to purchase 655,500 shares at $43.9999 each [1]. - The gross proceeds from the offering are expected to be approximately $250.8 million, before deducting underwriting discounts and commissions [1]. - The underwriters have a 30-day option to purchase up to an additional 855,000 shares at the public offering price [1]. Group 2: Use of Proceeds - The net proceeds from the offering will be used to advance Kymera's pipeline of preclinical and clinical degrader programs, as well as for working capital and other general corporate purposes [2]. Group 3: Company Background - Kymera Therapeutics is a clinical-stage biotechnology company focused on targeted protein degradation (TPD) to develop innovative medicines for significant health issues [6]. - The company aims to provide a new generation of effective therapies for patients with immunological diseases [6].

Core Insights - Kymera Therapeutics, Inc. (KYMR) faced a setback as partner Sanofi (SNY) decided not to advance the development of lead IRAK4 degrader KT-474, but this was somewhat mitigated by an exclusive option and license agreement with Gilead Sciences, Inc. (GILD) [1][8] - Kymera also announced a public offering of $250 million of its common stock to fund clinical programs and general corporate purposes [1][14] Group 1: Sanofi Partnership Update - Sanofi has chosen to advance KT-485/SAR447971, a new oral candidate targeting IRAK4 for immuno-inflammatory diseases, into clinical studies, while discontinuing KT-474, which was in phase IIb studies for hidradenitis suppurativa and atopic dermatitis [5][6] - Kymera achieved a $20 million milestone in Q2 2025 related to preclinical activities associated with KT-485 [7] - The decision to advance KT-485 delays potential milestone payments for Kymera that could have been realized with KT-474's approval [15] Group 2: Collaboration with Gilead - Kymera entered into an exclusive option and license agreement with Gilead for a novel molecular glue degrader (MGD) program targeting CDK2, with potential applications in oncology [10] - The agreement includes an upfront payment of $85 million and potential milestone payments up to $750 million [11] - Kymera may also receive tiered royalties ranging from high single-digit to mid-teens on net product sales, while leading all research activities for the CDK2 program [12] Group 3: Financial Developments - Kymera's stock decreased by 1.4% on June 25 and dropped 6.91% in after-market trading, likely due to the Sanofi setback and equity dilution from the stock offering [2] - Year-to-date, KYMR shares have gained 15.5%, contrasting with a 2% decline in the industry [4] - The proceeds from the $250 million stock offering will be used to advance preclinical and clinical degrader programs and for general corporate purposes [14]

Company Overview - Proactive is a financial news publisher that provides fast, accessible, informative, and actionable business and finance news content to a global investment audience [2] - The company has a team of experienced and qualified news journalists who produce independent content [2] Market Focus - Proactive specializes in medium and small-cap markets while also covering blue-chip companies, commodities, and broader investment stories [3] - The news team delivers insights across various sectors including biotech and pharma, mining and natural resources, battery metals, oil and gas, crypto, and emerging digital and EV technologies [3] Technology Adoption - Proactive is recognized for its forward-looking approach and enthusiastic adoption of technology to enhance workflows [4] - The company utilizes automation and software tools, including generative AI, while ensuring that all content is edited and authored by humans [5]

Financial Data and Key Metrics Changes - The meeting reported that proxies were received for approximately 61.66 million shares, representing about 94.68% of the total shares entitled to vote, indicating strong shareholder engagement [7] Business Line Data and Key Metrics Changes - No specific business line data or key metrics were discussed in the provided content Market Data and Key Metrics Changes - No specific market data or key metrics were discussed in the provided content Company Strategy and Development Direction and Industry Competition - The proposals included the election of directors and the approval of executive compensation, indicating a focus on governance and management alignment with shareholder interests [8][9] Management's Comments on Operating Environment and Future Outlook - No specific comments from management regarding the operating environment or future outlook were provided in the content Other Important Information - The meeting concluded with all proposals being carried, including the election of directors and the ratification of the independent accounting firm, Ernst and Young, for the fiscal year ending December 31, 2025 [14] Q&A Session Summary - There were no questions raised during the meeting, indicating a smooth process without shareholder concerns [12]

Core Insights - Sanofi has decided to advance Kymera's next-generation oral IRAK4 degrader candidate, KT-485, into clinical testing while not proceeding with KT-474 [1][3] - KT-485 has shown increased selectivity and potency with a favorable safety profile in preclinical testing [1][5] - Kymera is eligible for up to $975 million in collaboration milestones and has achieved a $20 million milestone related to preclinical activities for KT-485 [4][6] Company and Product Development - Kymera Therapeutics is a clinical-stage biopharmaceutical company focused on developing oral small molecule degrader medicines for immunological diseases [2][7] - KT-485, also known as SAR447971, is a first-in-class oral IRAK4 degrader aimed at treating immuno-inflammatory diseases [6] - The collaboration with Sanofi includes a 50/50 development and profit share option for KT-485 in the U.S. [1][4] Clinical and Market Potential - The advancement of KT-485 into Phase 1 testing is expected next year, reflecting its compelling preclinical profile [3][5] - The IRAK4 pathway is targeted due to its role as a master regulator of innate immunity, which could lead to a broad anti-inflammatory effect [6] - The collaboration aims to transform treatment paradigms in immunology by leveraging the unique properties of degraders compared to traditional small molecule inhibitors [5]