Key Takeaways KYMR stock soared 70.7% in 3 months, outperforming its industry and the broader market. A new $750M collaboration with GILD on CDK2 degraders has fueled investor enthusiasm. Despite a Sanofi setback, KYMR earned a $20M milestone and eyes key pipeline advances in 2025-2026.Shares of Kymera (KYMR) have surged 70.7% in the past three months compared with the industry’s gain of 9.7%. The stock has also outperformed the sector and the S&P 500 index during this timeframe.This clinical-stage biotec ...

Collaboration focuses on the discovery of novel, non-CRBN/VHL, Targeted Glue™ degraders for oncology and immunology indications At Amphista Therapeutics, we are focused on transforming the lives of patients with severe diseases, including cancer and neurodegenerative disorders, through the discovery of advanced, next generation targeted protein degradation (TPD) medicines. Amphista applies its proprietary Eclipsys® platform to generate unique, sequentially bifunctional Targeted Glue™ therapeutics with a dif ...

Agenda Kymera's Immunology Strategy Nello Mainolfi, PhD, Founder, President and Chief Executive Officer Oral Medicines with Biologics-like Activity Immunology Innovation Day May 9, 2025 STAT6 (KT-621) Update Jared Gollob, MD, Chief Medical Officer IRF5 (KT-579): Drugging a Genetically Validated Target Veronica Campbell, Senior Director, Immunology Question and Answer Session Forward Looking Statements This presentation contains forward-looking statements within the meaning of the Private Securities Litigati ...

January 2025 Revolutionizing Immunology: Oral Drugs with Biologics-Like Efficacy Science-driven clinical stage organization with industry-leading oral immunology pipeline J.P. Morgan Healthcare Conference Nello Mainolfi, Ph.D., Founder, President and CEO Forward Looking Statements This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and other federal securities laws. These statements include, but are not limited to, implied and expr ...

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]

June 2, 2025 KT-621 / STAT6 Degrader Phase 1 Healthy Volunteer Results Revolutionizing Immunology with Oral Small Molecule Degrader Medicines Agenda Introduction Justine Koenigsberg Vice President, Investor Relations Revolutionizing Immunology with Oral Medicines Nello Mainolfi, PhD Founder, President and Chief Executive Officer KT-621 Phase 1 Healthy Volunteer Data Jared Gollob, MD Chief Medical Officer Question and Answer Session 2 Forward Looking Statements This presentation contains forward-looking stat ...

Phase 1 healthy volunteer data of KT-621, a once-a-day STAT6 degrader, surpass Kymera’s target product profile, significantly derisking program and further validating its oral, biologics-like profile >90% mean STAT6 degradation in blood achieved at all doses above 1.5 mg Complete STAT6 degradation achieved in both blood and skin at all MAD doses ≥50 mg KT-621 impact on Th2 biomarkers in line or superior to dupilumab with median TARC reduction up to 37% and median Eotaxin-3 reduction up to 63% KT-621 was we ...

Company to host video webcast at 8:00 a.m. ET on Monday, June 2, 2025WATERTOWN, Mass., May 30, 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 announce results from the Phase 1 clinical trial evaluating single and multiple-ascending doses of KT-621 in healthy volunteers on Monday, June 2, 2025. The Company will host a video webcast at 8:00 a.m. ET tha ...