Kymera Results Presentation Deck
Tumor Volume (mm³)
Mean, +SEM
KT-333 Highly Active on Intermittent Dosing Regimens
Complete Tumor Regressions Associated with Robust STAT3 KD for ~48h in Preclinical Models
3000
2000
1000-
0
SU-DHL-1
Weekly Dosing
Vehicle
KT-333, 5 mg/kg, QW
KT-333, 10 mg/kg, QW
[ITHH
HH
10
5
15
Days (Post-randomization)
HH
20
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25
Dose- and degradation-dependent tumor growth
inhibition observed with once-weekly dosing in ALK+
ALCL
10 mg/kg sufficient to drive full tumor regression in
SU-DHL- 1 that was durable for multiple weeks after
the last dose (on day 14)
100000
KT-333 Concentration
(ng/ml or ng/g)
10000
1000
100
10
Preclinical PK/PD
•Tumor PK
48
Plasma PK
96
Time (hr)
144
Tumor PD
192
240
150
100
50
-0
Based on preclinical model (STAT3 dependent ALK+
ALCL), target PD >90% STAT3 KD for ~48 hours to
achieve robust anti-tumor activity
% of Vehicle Control
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