http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View Older Stories View More Recent Stories
-
Kymera Therapeutics to Report Second Quarter 2024 Financial Results on August 7
-
Kymera Therapeutics to Present in Fireside Chat at the UBS Virtual Targeted Protein Degradation Day
-
Kymera Therapeutics (KYMR) Announces Expansion of KT-474 HS and AD Phase 2 Studies
-
Kymera Announces Expansion of KT-474 (SAR444656) HS and AD Phase 2 Studies Following Interim Review of Safety and Efficacy
-
Biotechs Race to Develop New Treatments as Global Pancreatic Cancer Market Size Expected to Reach $7.5 Billion by 2033
-
Kymera Therapeutics (KYMR) Presents New Clinical Data from the Ongoing Phase 1 Trial of STAT3 Degrader KT-333 at EHA Annual Meeting
-
Kymera Therapeutics Presents New Clinical Data from the Ongoing Phase 1 Trial of STAT3 Degrader KT-333 at EHA Annual Meeting
-
Kymera Therapeutics Presents New Clinical Data from Ongoing Phase 1 Trial of MDM2 Degrader KT-253 at ASCO Annual Meeting
-
Kymera Therapeutics to Participate in Upcoming June Investor Conferences
-
Kymera Therapeutics to Participate in Upcoming June Investor Conferences
-
Kymera Therapeutics to Present New Clinical Data from Ongoing Phase 1 Trial of MDM2 Degrader KT-253 at ASCO Annual Meeting
-
Kymera Therapeutics Presents New Preclinical Data for KT-621, a First-In-Class, Oral STAT6 Degrader at the ATS Annual Meeting
-
Kymera Therapeutics to Present New Clinical Data from the Ongoing Phase 1 Trial of STAT3 Degrader KT-333 at EHA Annual Meeting
-
Kymera Therapeutics to Participate in Upcoming May Investor Conferences
-
Kymera Therapeutics Announces First Quarter 2024 Financial Results and Provides a Business Update
-
Kymera Therapeutics to Report First Quarter 2024 Financial Results on May 2
-
Kymera Therapeutics (KYMR) Announces Scientific Presentations at the American Association for Cancer Research
-
Kymera Therapeutics Announces Scientific Presentations at the American Association for Cancer Research 2024 Annual Meeting
-
Kymera Therapeutics (KYMR) Presents Preclinical Data for STAT6 and TYK2
-
Kymera Therapeutics Presents Preclinical Data for STAT6 and TYK2 First-In-Class, Oral Degrader Immunology Programs at the American Academy of Dermatology Annual Meeting
-
Kymera Therapeutics to Participate in Upcoming March Investor Conferences
-
Kymera Therapeutics Announces Fourth Quarter and Full Year 2023 Financial Results and Provides a Business Update
-
Kymera Therapeutics to Report Fourth Quarter and Full Year 2023 Financial Results on February 22
-
Kymera Therapeutics to Present in Fireside Chat at the Guggenheim Healthcare Conference
-
Kymera Therapeutics Outlines Key 2024 Objectives and Strategy to Progress Leading Portfolio of Immunology and Oncology Programs
-
R&D Day Highlights Kymera’s Immunology Strategy and Emerging Pipeline of Novel, First-in-Class Oral Degraders Addressing Multiple Highly Prevalent Immuno-inflammatory Diseases
-
R&D Day Highlights Kymera’s Immunology Strategy and Emerging Pipeline of Novel, First-in-Class Oral Degraders Addressing Multiple Highly Prevalent Immuno-inflammatory Diseases
-
Kymera Therapeutics to Present at the 42nd Annual J.P. Morgan Healthcare Conference on Tuesday, January 9, 2024
-
Kymera Therapeutics to Host Virtual Immunology R&D Day on January 4
-
Kymera Therapeutics to Host Virtual Immunology R&D Day on January 4
-
Kymera Therapeutics (KYMR) Presents Interim Results from STAT3 Degrader Phase 1 Trial
-
Kymera Therapeutics Presents Interim Results from STAT3 Degrader Phase 1 Clinical Trial at American Society of Hematology Annual Meeting
-
Kymera Therapeutics Announces First Patient Dosed in Phase 2 Atopic Dermatitis Clinical Trial of KT-474 (SAR444656), a First-in-Class, Investigational IRAK4 Degrader, Generating a $15 Million Payment
-
Kymera Therapeutics (KYMR) Announces Publication of Phase 1 Trial Results for KT-474
-
Kymera Therapeutics Announces Publication of Phase 1 Trial Results for KT-474 (SAR444656), a First-in-Class IRAK4 Degrader, in Nature Medicine
-
Kymera Therapeutics to Present New Clinical Data from the Phase 1 Trial of STAT3 Degrader KT-333 at the ASH Annual Meeting
-
Kymera Therapeutics Announces Third Quarter 2023 Financial Results and Provides a Business Update
-
Kymera Therapeutics to Participate in Upcoming November Investor Conferences
-
Kymera Therapeutics Announces First Patient Dosed in Phase 2 Hidradenitis Suppurativa Clinical Trial of KT-474 (SAR444656), a First-in-Class, Investigational IRAK4 Degrader, Generating $40 Million Pay
-
Kymera Therapeutics to Report Third Quarter 2023 Financial Results on November 2
-
Kymera Therapeutics (KYMR) Presents Preclinical Data Demonstrating Activity of MDM2 Degraders in Acute Myeloid Leukemia and Merkel Cell Carcinoma
-
Kymera Therapeutics Presents Preclinical Data Demonstrating Activity of MDM2 Degraders in Acute Myeloid Leukemia and Merkel Cell Carcinoma
-
Kymera Therapeutics (KYMR) Receives U.S. FDA Fast Track Designation for KT-333 for CTCL and R/R PTCL
-
Kymera Therapeutics Receives U.S. FDA Fast Track Designation for KT-333, a First-in-Class, Investigational STAT3 Degrader for the Treatment of Relapsed/Refractory Cutaneous T-Cell Lymphoma and Relapse
-
Kymera Therapeutics to Participate in Upcoming September Investor Conferences
-
Kymera Therapeutics Announces Second Quarter 2023 Financial Results and Provides a Business Update
-
Kymera Therapeutics to Report Second Quarter 2023 Financial Results on August 3
-
Kymera Therapeutics Receives FDA Orphan Drug Designation for KT-253, a Novel, Highly Potent and Selective MDM2 Degrader for the Treatment of Acute Myeloid Leukemia
-
Kymera Therapeutics' (KYMR) STAT3 Degrader KT-333 and IRAKIMiD Degrader KT-413 Demonstrate Desired Target Knockdown and Safety with Continued Dose Escalation in Ongoing Phase I Trials
-
Kymera Therapeutics’ STAT3 Degrader KT-333 and IRAKIMiD Degrader KT-413 Demonstrate Desired Target Knockdown and Safety with Continued Dose Escalation in Ongoing Phase I Clinical Trials

