Kymera Investor Day Presentation Deck
KT-474 Phase 1 Trial Design Includes HV and Patients
Double-blind, placebo-controlled, Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) trial
Endpoints
Three-part Phase 1 Design
1
SAD Portion
Healthy Volunteers
• 7 cohorts
(up to 56 adult
healthy subjects)
8 per cohort
(6:2 randomization)
Single dosing
(starting dose 25 mg)
2
MAD Portion
Healthy Volunteers
5 cohorts
(up to 60 adult
healthy subjects)
12 per cohort
(9:3 randomization)
• 14x daily doses
(starting dose 25 mg)
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3
MAD Portion
Patient Cohort
• 1 cohort
(up to 20 AD and
HS patients)
Open-label
14x daily doses
Primary
Secondary/
Exploratory
SAD & MAD
Exploratory
SAD & MAD
Exploratory
MAD Only
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Pharmacokinetic measures
(half-life, bioavailability)
• IRAK4 knockdown in PBMC
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Safety & tolerability
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Ex vivo response of whole
blood to TLR agonists (SAD &
MAD) and IL-1B (MAD only)
IRAK4 knockdown in skin biopsies
Proinflammatory cytokine and
chemokine levels in skin biopsies
(Patients only)
Plasma C-reactive protein (HV and
Patients) and cytokine levels
(Patients only)
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