Trial intelligence / Profile preview

KT-621 in healthy volunteers

NCT06673667Phase 1Completed

Sponsor
Kymera Therapeutics
Start
Oct 2024
Primary completion
Apr 2025
Modality
Bivalent/Multivalent Binders, PROTACs (E3 ligase recruitment)
Countries
1
01

Overview

Phase 1, randomised, double-blind trial comparing KT-621 with Placebo (2 arms). Primary endpoints: Adverse Events at 38 days, Hematology Laboratory Parameters at 38 days and 7 more. Started Oct 2024; status: completed.

02

Drugs

KT-621

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