Kymera Therapeutics to Announce KT-621 BroADen Phase 1b Atopic Dermatitis Trial Results on December 8, 2025
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.
Sentiment and the balance of points
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Rhea-AI Summary
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.
Details
News Market Reaction – KYMR
On Dec 8, the first trading day after this news, KYMR closed 41.55% above the previous close.
Data tracked by StockTitan Argus for the Dec 8 session.
Key Figures
- BroADen readout date
- December 8, 2025
- Phase 1b KT-621 atopic dermatitis trial results timing
- Current share price
- $66.56
- Price before Phase 1b readout announcement
- 52-week high
- $68.80
- Shares trading modestly below 52-week high pre-readout
- Cash balance
- $978.7M
- Cash, cash equivalents and marketable securities as of Sep 30, 2025 (10-Q)
- Q3 2025 net loss
- $82.175M
- Net loss in Q3 2025 per 10-Q
- Q3 2025 R&D expense
- $74.094M
- Research and development expense in Q3 2025
- Follow-on offering proceeds
- $288.4M
- Aggregate gross proceeds from June–July 2025 follow-on offering
- Potential Sanofi milestones
- $975M
- Future development, regulatory and commercial milestones under IRAK4 collaboration
Historical Context
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First patient dosed in BROADEN2 Phase 2b KT-621 AD trial.
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Participation in multiple December investor fireside chats.
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Q3 2025 results with strong cash and KT-621 clinical progress.
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Expanded November conference schedule and webcast availability.
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Announcement of Q3 2025 earnings release date and call details.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
phase 1b medical
atopic dermatitis medical
stat6 medical
oral small molecule degrader medical
webcast technical
AI-generated analysis. How Rhea-AI works. Not financial advice.
Company to host video conference call and webcast at 8:00 a.m. ET on Monday, December 8, 2025
WATERTOWN, Mass., Dec. 05, 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 BroADen Phase 1b clinical trial evaluating KT-621, its oral STAT6 degrader, in patients with moderate to severe atopic dermatitis (AD) on Monday, December 8, 2025. A press release detailing the results will be issued at 7:00 a.m. ET, followed by a video conference call and webcast at 8:00 a.m. ET.
To join the video call or view the livestreamed webcast, please register via this link, or visit “News and Events” in the Investors section of the Company’s website at www.kymeratx.com. A replay of the webcast and copy of the presentation will be available following the event.
About KT-621
KT-621 is an investigational, first-in-class, once daily, oral degrader of STAT6, the specific transcription factor responsible for IL-4/IL-13 signaling and the central driver of Type 2 inflammation. In the Phase 1 clinical study in healthy volunteers, KT-621 demonstrated complete STAT6 degradation in blood and skin following low daily oral doses, reductions of multiple disease relevant Type 2 biomarkers, and a safety profile undifferentiated from placebo. KT-621, the first STAT6-directed drug to enter clinical evaluation, has the potential to transform treatment paradigms for more than 130 million patients around the world, including children and adults, suffering from Type 2 diseases such as atopic dermatitis (AD), asthma, bullous pemphigoid (BP), chronic obstructive pulmonary disease (COPD), chronic rhinosinusitis with nasal polyps (CRSwNP), eosinophilic esophagitis (EoE), chronic spontaneous urticaria (CSU), and prurigo nodularis (PN), among others.
The Company’s KT-621 BROADEN2 Phase 2b trial in moderate to severe AD patients is ongoing, and patient dosing has commenced. Data is expected to be reported by mid-2027. The BREADTH Phase 2b trial in asthma is planned to start in the first quarter of 2026. These studies are intended to accelerate KT-621 development and enable dose selection for subsequent parallel Phase 3 registration studies across multiple Type 2 dermatology, gastroenterology and respiratory indications.
About Kymera Therapeutics
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X or LinkedIn.
Investor and Media Contact:
Justine Koenigsberg
Vice President, Investor Relations
investors@kymeratx.com
media@kymeratx.com
857-285-5300
FAQ
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