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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 from Sanofi
2023-12-15
Atopic Dermatitis (AD) trial is the second KT-474 Phase 2 clinical trial to begin enrolling patients this quarter following trial in Hidradenitis Suppurativa (HS) Topline Phase 2 data from both the AD
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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 Payment from Sanofi
2023-10-31
The dosing of the first patient in the Phase 2 Atopic Dermatitis (AD) clinical trial is expected later this quarterWATERTOWN, Mass., Oct. 27, 2023 (GLOBE N
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Kymera and its partner Sanofi announced plans to initiate a Phase 2 clinical trial of IRAK4 degrader KT474/SAR444656 in HS in the fourth quarter of 2023
2023-09-25
Recently, Kymera and its partner Sanofi announced plans to initiate a Phase 2 clinical trial of the IRAK4 degrader KT474/SAR444656 in HS in the fourth quarter of 2023. This news further confirms the s
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Kymera Therapeutics Presents Clinical Data from the Phase 1 Trial of IRAK4 Degrader, KT-474 (SAR444656), at the European Academy of Dermatology and Venereology Symposium
2023-05-18
In the Phase 1 trial, KT-474 showed evidence of robust IRAK4 degradation in blood and skin lesions as well as a systemic anti-inflammatory effect in hidradenitis suppurativa (HS) and atopic dermatitis
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Kymera Announces Positive Results from Phase 1 Clinical Trial Evaluating KT-474 in Patients with HS and AD and Sanofi's Decision to Advance KT-474 into Phase 2 Clinical Trials
2022-12-23
KT-474 Phase 1 clinical data in HS and AD patients demonstrate robust IRAK4 knockdown in blood and active skin lesions and systemic suppression of proinflammatory cytokines and chemokines with a favorable safety profile Clinical endpoints addressing disease burden and symptoms demonstrate a highly competitive profile after four weeks of dosing, with substantial responses in majority of both HS and AD patients Modest, non-adverse QTc prolongation spontaneously resolves back to baseline during the 4-week dosing period Sanofi has committed to advance KT-474 (SAR444656) into Phase 2 clinical trials
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Kymera Therapeutics to Hold Investor Webcast on December 14 to Share Clinical Data from KT-474 Phase I Patient Cohorts and Oncology Pipeline
2022-10-13
Dosing in KT-474 Phase 1 HS and AD patient cohort (Part C) complete KT-413 and KT-333 continuing in Phase 1 dose escalationKT-253 has completed IND enabling studiesWATERTOWN, Mass., Oct. 13, 2022 (GLO
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