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Phase I, Phase I

Phase 1 Trial of the Safety, Pharmacokinetics, Pharmacodynamics, and Preliminary Clinical Activity of RP-1664 in Participants With Advanced Solid Tumors

What is the purpose of this trial?

The primary objective of this study is to identify a safe and tolerated dose and schedule of the orally administered PLK4 inhibitor RP-1664. In addition, this study will examine the pharmacokinetics (PK), pharmacodynamics (PD) and preliminary anti-tumor activity of RP-1664 in advanced solid tumors.

Contact Information

For more information about this study, including how to volunteer, contact Ingrid Palma

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  • Last Updated
    09/10/2024
  • Study HIC
    #2000037177