A Phase I Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of HH30134 in Patients With Advanced Solid Tumours

  • participants needed
  • sponsor
    Haihe Biopharma Co., Ltd.
Updated on 31 January 2023


The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and to determine the maximum tolerable dose (MTD) and/or recommended phase 2 dose (RP2D) of HH30134 administered orally on a continuous once daily (QD) schedule in adults patients with advanced solid tumors.

Condition Advanced Solid Tumors
Treatment HH30134
Clinical Study IdentifierNCT04746612
SponsorHaihe Biopharma Co., Ltd.
Last Modified on31 January 2023

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