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 that the U.S. FDA granted Fast Track designation to KT-621, a first-in-class oral STAT6 degrader for moderate to severe atopic dermatitis (AD), on December 11, 2025.
Fast Track follows positive BroADen Phase 1b AD results showing STAT6 degradation, biomarker modulation, clinical activity and supportive safety. The KT-621 BROADEN2 Phase 2b AD trial is ongoing with data expected by mid-2027, and the BREADTH Phase 2b asthma trial is planned to start in 1Q 2026. The company intends these studies to enable dose selection for parallel Phase 3 registration studies across Type 2 indications.
Kymera Therapeutics (NASDAQ: KYMR) priced an upsized underwritten public offering of 7,000,000 shares at $86.00 per share, raising approximately $602.0 million in gross proceeds; underwriters have a 30‑day option to buy up to an additional 1,050,000 shares at the offering price, less discounts and commissions.
The offering is expected to close on December 11, 2025, subject to customary conditions. Net proceeds are intended to fund advancement of preclinical and clinical degrader programs and for working capital and general corporate purposes. The offering is made from an effective Form S-3 shelf registration filed October 31, 2024.
Kymera Therapeutics (NASDAQ: KYMR) commenced a proposed underwritten public offering of $500.0 million of common stock, with a 30-day underwriter option to purchase up to an additional $75.0 million.
The offering is subject to market and other conditions and may not be completed as proposed. Kymera intends to use net proceeds to advance its preclinical and clinical degrader programs and for working capital and general corporate purposes. The securities are offered under an effective Form S-3 shelf registration (No. 333-282912).
Kymera Therapeutics (NASDAQ: KYMR) reported positive Phase 1b BroADen results for KT-621, an oral STAT6 degrader, in 22 moderate‑to‑severe atopic dermatitis patients dosed for 28 days.
Key data: median STAT6 degradation of 98% in blood and 94% in skin; mean EASI reduction of 63%; median TARC reduction of 74% in patients with baseline TARC comparable to dupilumab studies; FeNO reductions up to 56% in patients with asthma. Safety: no serious adverse events, no treatment‑related TEAEs, and no conjunctivitis reported. BROADEN2 Phase 2b in AD is ongoing with data expected by mid‑2027; BREADTH Phase 2b in asthma planned to start 1Q26.
Kymera Therapeutics (NASDAQ: KYMR) will announce topline results from the BroADen Phase 1b trial of KT-621, an oral STAT6 degrader for moderate to severe atopic dermatitis, on Monday, December 8, 2025.
A press release will be issued at 7:00 a.m. ET, followed by a video conference call and webcast at 8:00 a.m. ET. A replay and presentation will be available after the event. Investors can register via the company website at www.kymeratx.com under News and Events.
Kymera Therapeutics (NASDAQ: KYMR) announced dosing has begun in the BROADEN2 Phase 2b trial of KT-621, an oral STAT6 degrader for moderate to severe atopic dermatitis (AD). The randomized, double-blind, placebo-controlled, dose-ranging study will enroll ~200 patients treated over 16 weeks with three dose arms and a primary endpoint of percent change in EASI score at Week 16.
The company expects BROADEN2 data by mid-2027, completed dosing in the Phase 1b BroADen trial with data due December 2025, and plans to initiate the BREADTH Phase 2b asthma trial in 1Q 2026. Patients may enter a 52-week open-label extension after the trial.
Kymera Therapeutics (NASDAQ: KYMR) will participate in three investor fireside chats in early December 2025: Piper Sandler 37th Annual Healthcare Conference in New York on Dec 2 at 2:30 p.m. ET, Citi 2025 Global Healthcare Conference in Miami on Dec 3 at 11:15 a.m. ET, and Evercore 8th Annual Healthcare Conference in Coral Gables on Dec 4 at 8:45 a.m. ET. Live webcasts and archived replays will be available in the Investors "News and Events" section at www.kymeratx.com.
Kymera Therapeutics (NASDAQ: KYMR) reported third-quarter 2025 results and pipeline progress. Key financials include cash of $978.7 million as of September 30, 2025, and an expected cash runway into the second half of 2028. The company posted a net loss of $82.2 million with R&D expense of $74.1 million in Q3.
Clinical highlights: KT-621 completed enrollment and dosing in the BroADen Phase 1b atopic dermatitis study with data expected in December 2025, initiated the BROADEN2 Phase 2b in AD, and is on track to start the BREADTH Phase 2b asthma trial in 1Q 2026. KT-579 completed IND-enabling studies with Phase 1 expected in early 2026.
Kymera Therapeutics (NASDAQ: KYMR) will participate in multiple investor fireside chats in November 2025. Events and times: Guggenheim Healthcare Innovation in Boston on Nov 10, 9:00 AM ET; UBS 2025 Global Healthcare in Palm Beach on Nov 10, 11:45 AM ET; Stifel 2025 Healthcare in New York on Nov 11, 1:20 PM ET; TD Cowen Virtual Immunology & Inflammation Summit on Nov 13, 10:30 AM ET; and Jefferies Global Healthcare in London on Nov 19, 11:00 AM GMT.
Live webcasts and replay archives will be available under News and Events in the Investors section of the company's website at www.kymeratx.com.
Kymera Therapeutics (NASDAQ: KYMR) will report third quarter 2025 financial results on November 4, 2025.
The company will host a video conference call and livestreamed webcast on November 4, 2025 at 8:30 a.m. ET. Investors can register to join the video call or view the webcast via the company’s Investors > News and Events page at www.kymeratx.com. A replay of the webcast will be archived and available after the event.