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. (NASDAQ: KYMR) is a clinical-stage biotechnology company advancing a pipeline of oral small molecule degrader medicines based on targeted protein degradation (TPD). This news page aggregates company announcements, clinical updates, collaboration developments and capital markets activity related to Kymera’s work in immunological and other serious diseases.
Readers can follow detailed updates on KT-621, Kymera’s investigational first-in-class oral STAT6 degrader in Phase 2 clinical testing for Type 2 inflammatory diseases such as atopic dermatitis and asthma. News items include Phase 1b and Phase 2 trial progress, biomarker and clinical endpoint data, and regulatory milestones such as U.S. FDA Fast Track designation for moderate to severe atopic dermatitis. Coverage also extends to KT-579, an investigational oral IRF5 degrader for immune-mediated conditions, as it moves from preclinical work toward first-in-human studies.
In addition to internal programs, this feed highlights updates on Kymera’s partnered assets, including the IRAK4 degrader KT-485/SAR447971 in collaboration with Sanofi for immuno-inflammatory diseases and the oral CDK2 molecular glue degrader program with Gilead Sciences for potential use in breast cancer and other solid tumors. Investors can also find information on public offerings of common stock, shelf registration statements, and other corporate events disclosed through press releases and SEC filings.
By reviewing Kymera news on this page, users can track clinical trial milestones, regulatory interactions, collaboration announcements and financing transactions that shape the company’s development trajectory. For those researching KYMR stock or the evolution of targeted protein degradation in immunology and oncology, this consolidated news view provides ongoing context around Kymera’s pipeline and corporate strategy.
Kymera Therapeutics (NASDAQ: KYMR) announced a virtual investor event scheduled for December 14, 2022, where they will share clinical updates on their Phase 1 trial of the IRAK4 degrader KT-474. This trial targets patients with hidradenitis suppurativa or atopic dermatitis. Additionally, the company will discuss its oncology pipeline developments. Kymera focuses on targeted protein degradation to develop innovative therapies for various diseases, leveraging its proprietary Pegasus platform.
Kymera Therapeutics (NASDAQ: KYMR) announced substantial developments in its clinical programs and financial status. The company completed the patient cohort of the KT-474 Phase 1 trial, focusing on autoimmune diseases, and is on track for regulatory submissions for KT-253. In Q3 2022, Kymera raised $150 million in private equity, closing with a cash balance of $596 million, projected to sustain operations into 2025. However, collaboration revenues fell to $9.6 million from $20.3 million year-over-year, contributing to a net loss of $43 million.
Kymera Therapeutics (NASDAQ: KYMR) appointed Dr. Victor Sandor to its Board of Directors on November 3, 2022, to leverage his extensive experience in biopharmaceutical clinical development. Dr. Sandor, previously Chief Medical Officer at Array BioPharma, is expected to enhance Kymera’s capabilities in advancing targeted protein degradation therapies. The company acknowledged the contributions of retiring board member Don Nicholson, PhD, who has served for five years. Kymera aims to capitalize on its Pegasus platform to develop innovative treatments for various diseases.
Kymera Therapeutics (NASDAQ: KYMR) will announce its Q3 2022 financial results on November 3, 2022, hosting a conference call at 8:30 a.m. ET. The company is also set to participate in several investor conferences, including:
- Credit Suisse Annual Healthcare Conference on November 9
- Stifel Healthcare Conference on November 15
- Piper Sandler Healthcare Conference from November 29 to December 1
- Bank of America Biotech Conference on December 7
Access the call at kymeratx.com.
Kymera Therapeutics (NASDAQ: KYMR) has completed dosing in Part C of its Phase 1 clinical trial for KT-474, aimed at treating hidradenitis suppurativa (HS) and atopic dermatitis (AD). This Phase 1 trial showcases positive pharmacokinetics and safety results. Concurrently, the company continues dose escalation for KT-333 and KT-413, both targeting cancer indications. Additionally, IND enabling studies for KT-253 are complete, with an expected IND filing by year-end. A webcast on December 14 will present further details on clinical data and development pipelines.
Kymera Therapeutics (NASDAQ: KYMR) announced on September 15, 2022, that the FDA has granted orphan drug designation for its candidate KT-333 to treat Cutaneous T-cell Lymphoma (CTCL). This marks the second orphan designation for KT-333, which is a first-in-class STAT3 degrader. Currently, no approved therapies specifically target this pathway in CTCL. The FDA's designation allows for various development incentives such as tax credits and seven-year marketing exclusivity upon approval. The ongoing Phase 1 trial for KT-333 evaluates its safety in patients with aggressive lymphomas.
Kymera Therapeutics (NASDAQ: KYMR) announced that its Co-Founder, President, and CEO, Nello Mainolfi, will participate in several upcoming investor conferences. Key events include the 2022 Wells Fargo Healthcare Conference on September 7 at 1:20 p.m. ET, the Morgan Stanley 20th Annual Global Healthcare Conference on September 14 at 8:00 a.m. ET, and the 2022 Guggenheim Nantucket Therapeutics Conference on September 28 at 2:15 p.m. ET. Presentation webcasts will be accessible on Kymera's website, with archived replays available for 90 days.
Kymera Therapeutics (NASDAQ: KYMR) has announced a PIPE financing, issuing 2,769,228 shares of common stock at $26.00 each and pre-funded warrants for 3,000,000 shares at $25.9999. The anticipated gross proceeds of approximately $150 million will support ongoing R&D and general corporate needs. The financing is led by notable healthcare investors and is expected to close on August 22, 2022. Following the transaction, Kymera's cash reserves are projected to exceed $600 million by August 31, 2022.
Kymera Therapeutics (NASDAQ: KYMR) initiated dosing in Part C of its Phase 1 clinical trial for the IRAK4 degrader KT-474, aiming to share data by year-end 2022. The company has also launched Phase 1 trials for oncology programs KT-333 and KT-413, with results expected soon. As of June 30, 2022, Kymera reported a cash balance of approximately $482.5 million, providing a runway into 2025. Despite an increase in research and development expenses leading to a net loss of $40.3 million for Q2 2022, the company remains on track for significant clinical milestones this year.
Kymera Therapeutics, a clinical-stage biopharmaceutical company, is set to reveal its second quarter 2022 financial results on August 9, 2022. A conference call will follow at 8:30 a.m. ET, accessible via phone or a live webcast on their website. The company focuses on targeted protein degradation, utilizing its Pegasus platform to develop novel therapies for treating various immune-inflammatory diseases and cancers. Founded in 2016 and headquartered in Watertown, Mass., Kymera has gained recognition as an industry leader.
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