Welcome to our dedicated page for Kymera Therapeutics news (Ticker: KYMR), a resource for investors and traders seeking the latest updates and insights on Kymera Therapeutics stock.
Kymera Therapeutics, Inc. (KYMR) is a clinical-stage biopharmaceutical company advancing targeted protein degradation therapies for immune-inflammatory diseases and oncology. This dedicated news hub provides investors and industry observers with timely updates on the company’s scientific progress, clinical developments, and strategic initiatives.
Access comprehensive coverage of KYMR’s innovative pipeline, including updates on STAT6 and IRAK4 degrader programs, partnership announcements, and financial disclosures. Our curated news collection enables efficient tracking of milestones in protein degradation research – from preclinical breakthroughs to clinical trial results – while maintaining strict adherence to factual reporting standards.
Key content categories include regulatory filings, peer-reviewed research highlights, executive leadership updates, and analysis of therapeutic platform advancements. All materials are sourced from verified channels to ensure reliability for investment research and sector analysis.
Bookmark this page for streamlined access to KYMR’s latest developments in transforming undruggable targets into viable treatment pathways through proprietary degradation technology. Check regularly for updates on oral small molecule therapies that aim to combine biologics-like efficacy with enhanced patient convenience.
Kymera Therapeutics (NASDAQ: KYMR) reported significant progress in its clinical trials for novel protein degrader drugs. In a Phase 1 trial, KT-474, an IRAK4 degrader, achieved up to 96% degradation in blood and 97% inhibition of pro-inflammatory cytokines. The FDA cleared its IND application for KT-333, its STAT3 degrader, expected to enter clinical trials by year-end 2021. The company will host a virtual R&D Day on December 16, announcing further data and plans for its drug pipeline.
Kymera Therapeutics (NASDAQ: KYMR) announced the presentation of preclinical data on its STAT3 degrader program at the upcoming Society for Immunotherapy of Cancer (SITC) and American Society of Hematology (ASH) Annual Meetings. The data focuses on the treatment potential for hematological malignancies and solid tumors. The lead candidate, KT-333, is nearing a Phase 1 trial. The findings suggest synergistic effects when combining STAT3 degraders with immune checkpoint inhibitors, promising advancements in treating previously undruggable cancers.
Kymera Therapeutics, Inc. (NASDAQ: KYMR), a clinical-stage biopharmaceutical company, announced its participation in several upcoming virtual investor conferences. Notable events include a panel discussion at the UBS conference on November 1, 2021, and fireside chats at the Credit Suisse and Stifel healthcare conferences on November 11 and 15, respectively. Kymera focuses on targeted protein degradation, with its Pegasus™ platform addressing high-impact targets for immune-inflammatory diseases and cancers. For more details, webcasts will be available on their website.
Kymera Therapeutics (NASDAQ: KYMR) announced promising results from its Phase 1 trial of KT-474, a selective IRAK4 degrader. The Single Ascending Dose (SAD) trial showed up to 96% mean reduction of IRAK4 in PBMC within 48 hours, and up to 97% inhibition of pro-inflammatory cytokines. KT-474 was well-tolerated across all dose levels, with no serious adverse events reported. The MAD portion is underway, evaluating daily dosing. Kymera plans to present additional data before year-end, advancing its aim to target immune-inflammatory diseases.
Kymera Therapeutics (NASDAQ: KYMR) announced a conference call and webcast on October 27 to review data from the Single Ascending Dose (SAD) phase of the KT-474 trial. This presentation will feature Dr. Jared Gollob, the Chief Medical Officer, and will begin at 8:30 a.m. ET, followed by the conference call at 10:30 a.m. ET. The event aims to discuss Kymera's advancements in targeted protein degradation therapies, particularly for immune-inflammatory diseases and malignancies, highlighting its innovative Pegasus™ platform.
Kymera Therapeutics (NASDAQ: KYMR) announced multiple presentations at the 4th Annual Targeted Protein Degradation Summit from October 26-29, 2021. Keynote presentations will detail safety, pharmacokinetics (PK), and pharmacodynamics (PD) data from the Single Ascending Dose (SAD) phase of the KT-474 Phase 1 trial in healthy volunteers. KT-474, an orally available IRAK4 degrader, targets immune-inflammatory diseases like rheumatoid arthritis. The company plans to present further data from the Multiple Ascending Dose (MAD) phase by year-end.
Kymera Therapeutics (NASDAQ: KYMR), a clinical-stage biopharmaceutical company, announced participation in two upcoming investor conferences. The first is the Morgan Stanley 19th Annual Global Healthcare Conference, featuring a live webcast on September 9, 2021, at 1:15 p.m. ET. The second is the H.C. Wainwright 23rd Annual Global Investment Conference, with an on-demand presentation available from September 13, 2021, at 7:00 a.m. ET. Webcasts can be accessed on the Company's website, where archived versions will be available for 30 days.
Kymera Therapeutics (NASDAQ: KYMR) reported positive interim results from its Phase 1 trial of KT-474, a first-in-class oral IRAK4 degrader, demonstrating a 94% degradation rate. The company initiated dosing for the Multiple Ascending Dose (MAD) portion of the trial and expects Investigational New Drug Applications (IND) for KT-413 and KT-333 in 2H 2021. Following a successful follow-on offering, Kymera now has a pro forma cash position of $647 million to support ongoing development and pipeline expansion. Collaboration revenues rose to $18.5 million while net loss for Q2 2021 was $24.7 million.
Kymera Therapeutics (NASDAQ: KYMR) announced the appointments of Karen Weisbach as Vice President of People and Culture and Jolly Bhatia as Vice President of Quality. Weisbach brings over 15 years of HR experience from bluebird bio, focusing on talent strategies. Bhatia, with 25 years in quality oversight, previously held roles at X4 Pharmaceuticals and Alnylam Pharmaceuticals. These appointments are part of Kymera's effort to strengthen its capabilities in targeted protein degradation and expand its pipeline, which targets immune-inflammatory diseases and various cancers.